Pacira BioSciences, Inc. v. Fortis Advisors LLC
This text of Pacira BioSciences, Inc. v. Fortis Advisors LLC (Pacira BioSciences, Inc. v. Fortis Advisors LLC) is published on Counsel Stack Legal Research, covering Court of Chancery of Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.
Opinion
IN THE COURT OF CHANCERY OF THE STATE OF DELAWARE
PACIRA BIOSCIENCES, INC. and ) PACIRA CRYOTECH, INC., ) ) Plaintiffs/Counterclaim- ) Defendants, ) ) v. ) C.A. No. 2020-0694-PAF ) FORTIS ADVISORS LLC, solely in its ) capacity as representative of the former ) securityholders of MYOSCIENCE, INC., ) ) Defendant/Counterclaim- ) Plaintiff. )
MEMORANDUM OPINION
Date Submitted: March 11, 2024 Date Decided: January 21, 2025
Lisa A. Schmidt, Raymond J. DiCamillo, Kevin M. Kidwell, RICHARDS, LAYTON & FINGER, P.A., Wilmington, Delaware; Anne Champion, Zainab Ahmad, Timothy Sun, Maya Danaher, GIBSON, DUNN & CRUTCHER LLC, New York, New York; Attorneys for Plaintiffs/Counterclaim-Defendants Pacira BioSciences, Inc. and Pacira CryoTech, Inc.
Lauren K. Neal, Courtney Kurz, MORRIS, NICHOLS, ARSHT & TUNNELL LLP, Wilmington, Delaware; Christopher J. Marino, Taylor P. Lovejoy, DAVIS MALM & D’AGOSTINE, P.C., Boston, Massachusetts; Attorneys for Defendant/Counterclaim-Plaintiff Fortis Advisors LLC.
FIORAVANTI, Vice Chancellor Two corporations agreed that it would be in their mutual interest for one to
acquire the other but were unable to agree on an up-front purchase price. To bridge
the gap, they attempted to create objective milestones to measure the target’s success
in the following years and conditioned almost half of the merger consideration on
achievement of certain conditions. After closing, a dispute arose over whether some
of those conditions had been triggered. In other words, this is an earnout case.
This is, for the parties, a $30 million question. For the court, it is one of
contract interpretation. At issue in this post-trial opinion are the meanings of two
phrases in the earnout provision. Under the contract, certain earnout payments are
tied to the reimbursement rate for a medical procedure using the target’s device.
Reimbursement rates are set using procedural code numbers, and they vary based on
the care setting and by locality. The parties dispute whether the contract ties the
earnout payment to a national benchmark reimbursement rate or a locality-adjusted
reimbursement rate. The buyer insists that the contract contemplates use of a
national rate. The sellers argue that local rates control. On this issue, the court
concludes that the contract is ambiguous and that the extrinsic evidence
overwhelmingly supports the buyer’s interpretation.
The parties also dispute whether the applicable reimbursement rate is tied to
a single, specific reimbursement code or could be triggered by multiple
reimbursement codes. On this issue, the contract is unambiguous, and the earnout is not limited to a single, specific reimbursement code. Nevertheless, the sellers
have not proved, as a matter of fact, that the earnout was triggered under their other
proffered codes. Accordingly, judgment will be entered in favor of the buyer.
I. BACKGROUND These are the facts as the court finds them after trial.1
A. The Parties
In 2019, Pacira Biosciences, Inc. (“Pacira”) acquired MyoScience, Inc.
(“MyoScience”). 2 At the time of the merger, MyoScience had one product: iovera®
(“iovera”), a handheld medical device used primarily for pain relief. 3
The terms of the acquisition are contained in an Agreement and Plan of
Merger, dated March 4, 2019, by and among Pacira Pharmaceuticals, Inc., 4 PS
Merger, Inc., MyoScience, and Fortis Advisors LLC (“Fortis”), as the
1 Other factual findings are contained in the analysis of the claims. The trial record consists of trial testimony from ten witnesses, deposition testimony from 15 witnesses, and 248 exhibits. Deposition testimony is cited as “(Surname) Dep.”; trial exhibits are cited as “JX”; stipulated facts in the pre-trial order are cited as “PTO”; and references to the docket are cited as “Dkt.,” with each followed by the relevant section, page, paragraph, exhibit, or docket number. Trial testimony is cited in the form “Tr. (X),” with “X” representing the surname of the speaker. After being identified initially, individuals are referenced herein by their surnames without regard to formal titles such as “Dr.” No disrespect is intended. 2 PTO ¶¶ 43, 79. Pacira CryoTech, Inc. is the successor to MyoScience. Id. ¶ 41. 3 Id. ¶¶ 69–70; JX 2 at 2. 4 Pacira Pharmaceuticals, Inc. changed its name to Pacira Biosciences, Inc. (i.e., Pacira) after the merger. PTO ¶ 2 n.1.
2 Securityholders’ Representative (the “Merger Agreement”).5 Fortis serves as the
representative for certain former MyoScience securityholders, including the
beneficiaries of the earnout payments at issue in this action. 6 A group of former
MyoScience securityholders directs Fortis’s actions with respect to the Merger
Agreement (the “Advisory Group”). 7
B. CPT Codes and CMS Reimbursement Rates When billing for a medical procedure, health care providers must submit a bill
for their services using standardized diagnosis and procedure codes.8 Among these
procedure codes are Category I Current Procedural Terminology (“CPT”) codes,
numerical codes ranging from CPT code 00100 to 99499, each of which corresponds
to a specific procedure. 9 The American Medical Association (“AMA”) defines and
updates the CPT codes. 10 The Centers for Medicare and Medicaid (“CMS”) set, and
5 JX 101. 6 Id. at 6, 17–18, 105, 114; PTO ¶ 42. 7 PTO ¶ 44. The current members of the Advisory Group are Brian Farley, Valiance Asset Management Ltd. (“Valiance”), and AMV Partners I, L.P. (“AMV”). Id. Farley was the chair of MyoScience’s board of directors from April 2018 until the merger. Id. ¶ 51. Jan Pensaert is Valiance’s designee and Anthony Lando is AMV’s designee. Id. ¶ 44. The original members of the Advisory Group were Lando, Pensaert, and Timothy Still. Id. Still was MyoScience’s chief executive officer from October 2018 until the merger. Id. ¶ 50. Still left the Advisory Group after he was served as a defendant under the original complaint in this action in August 2020. Id. ¶ 44. 8 Id. ¶ 59. 9 Id. ¶ 60. 10 Id. ¶¶ 4, 19.
3 annually update, how much Medicare—a major insurance provider—will reimburse
health care providers for each CPT-coded procedure. 11 The amount Medicare pays
for a procedure varies depending on the care setting, resulting in different rates in
hospital outpatient, ambulatory surgery center (“ASC”), and physician’s office
settings.12 That, however, is not the only variable.
CMS releases “national” reimbursement rates for each CPT code, but the
national reimbursement rate is not the exact amount a medical professional would
receive from Medicare if reimbursed for the procedure. 13 Care providers are paid
based on a calculation that produces a “locality-adjusted” reimbursement rate that
takes into account the relative cost of care in the geographic location where the
patient is served.14 For example, in 2020, the geographic wage index of different
places across the country ranged from 0.7543 to 1.8551.15 Thus, depending on
where a procedure was performed, the amount that Medicare would reimburse a
medical professional could vary significantly. 16 By contrast, the artificial national
11 Id. ¶ 61; Tr. 15:10–11 (Stack). 12 PTO ¶ 61. 13 “The existence of a CPT code does not guarantee payment of any particular procedure. Payment of any procedure by Medicare is predicated, for example, on the medical necessity of the service and adequate documentation of the procedure.” Id. ¶ 63. 14 Id. ¶ 64. 15 JX 231 ¶ 59. 16 Id. ¶¶ 57–60.
4 reimbursement rate assigned to each CPT code is the dollar value output if all
Free access — add to your briefcase to read the full text and ask questions with AI
IN THE COURT OF CHANCERY OF THE STATE OF DELAWARE
PACIRA BIOSCIENCES, INC. and ) PACIRA CRYOTECH, INC., ) ) Plaintiffs/Counterclaim- ) Defendants, ) ) v. ) C.A. No. 2020-0694-PAF ) FORTIS ADVISORS LLC, solely in its ) capacity as representative of the former ) securityholders of MYOSCIENCE, INC., ) ) Defendant/Counterclaim- ) Plaintiff. )
MEMORANDUM OPINION
Date Submitted: March 11, 2024 Date Decided: January 21, 2025
Lisa A. Schmidt, Raymond J. DiCamillo, Kevin M. Kidwell, RICHARDS, LAYTON & FINGER, P.A., Wilmington, Delaware; Anne Champion, Zainab Ahmad, Timothy Sun, Maya Danaher, GIBSON, DUNN & CRUTCHER LLC, New York, New York; Attorneys for Plaintiffs/Counterclaim-Defendants Pacira BioSciences, Inc. and Pacira CryoTech, Inc.
Lauren K. Neal, Courtney Kurz, MORRIS, NICHOLS, ARSHT & TUNNELL LLP, Wilmington, Delaware; Christopher J. Marino, Taylor P. Lovejoy, DAVIS MALM & D’AGOSTINE, P.C., Boston, Massachusetts; Attorneys for Defendant/Counterclaim-Plaintiff Fortis Advisors LLC.
FIORAVANTI, Vice Chancellor Two corporations agreed that it would be in their mutual interest for one to
acquire the other but were unable to agree on an up-front purchase price. To bridge
the gap, they attempted to create objective milestones to measure the target’s success
in the following years and conditioned almost half of the merger consideration on
achievement of certain conditions. After closing, a dispute arose over whether some
of those conditions had been triggered. In other words, this is an earnout case.
This is, for the parties, a $30 million question. For the court, it is one of
contract interpretation. At issue in this post-trial opinion are the meanings of two
phrases in the earnout provision. Under the contract, certain earnout payments are
tied to the reimbursement rate for a medical procedure using the target’s device.
Reimbursement rates are set using procedural code numbers, and they vary based on
the care setting and by locality. The parties dispute whether the contract ties the
earnout payment to a national benchmark reimbursement rate or a locality-adjusted
reimbursement rate. The buyer insists that the contract contemplates use of a
national rate. The sellers argue that local rates control. On this issue, the court
concludes that the contract is ambiguous and that the extrinsic evidence
overwhelmingly supports the buyer’s interpretation.
The parties also dispute whether the applicable reimbursement rate is tied to
a single, specific reimbursement code or could be triggered by multiple
reimbursement codes. On this issue, the contract is unambiguous, and the earnout is not limited to a single, specific reimbursement code. Nevertheless, the sellers
have not proved, as a matter of fact, that the earnout was triggered under their other
proffered codes. Accordingly, judgment will be entered in favor of the buyer.
I. BACKGROUND These are the facts as the court finds them after trial.1
A. The Parties
In 2019, Pacira Biosciences, Inc. (“Pacira”) acquired MyoScience, Inc.
(“MyoScience”). 2 At the time of the merger, MyoScience had one product: iovera®
(“iovera”), a handheld medical device used primarily for pain relief. 3
The terms of the acquisition are contained in an Agreement and Plan of
Merger, dated March 4, 2019, by and among Pacira Pharmaceuticals, Inc., 4 PS
Merger, Inc., MyoScience, and Fortis Advisors LLC (“Fortis”), as the
1 Other factual findings are contained in the analysis of the claims. The trial record consists of trial testimony from ten witnesses, deposition testimony from 15 witnesses, and 248 exhibits. Deposition testimony is cited as “(Surname) Dep.”; trial exhibits are cited as “JX”; stipulated facts in the pre-trial order are cited as “PTO”; and references to the docket are cited as “Dkt.,” with each followed by the relevant section, page, paragraph, exhibit, or docket number. Trial testimony is cited in the form “Tr. (X),” with “X” representing the surname of the speaker. After being identified initially, individuals are referenced herein by their surnames without regard to formal titles such as “Dr.” No disrespect is intended. 2 PTO ¶¶ 43, 79. Pacira CryoTech, Inc. is the successor to MyoScience. Id. ¶ 41. 3 Id. ¶¶ 69–70; JX 2 at 2. 4 Pacira Pharmaceuticals, Inc. changed its name to Pacira Biosciences, Inc. (i.e., Pacira) after the merger. PTO ¶ 2 n.1.
2 Securityholders’ Representative (the “Merger Agreement”).5 Fortis serves as the
representative for certain former MyoScience securityholders, including the
beneficiaries of the earnout payments at issue in this action. 6 A group of former
MyoScience securityholders directs Fortis’s actions with respect to the Merger
Agreement (the “Advisory Group”). 7
B. CPT Codes and CMS Reimbursement Rates When billing for a medical procedure, health care providers must submit a bill
for their services using standardized diagnosis and procedure codes.8 Among these
procedure codes are Category I Current Procedural Terminology (“CPT”) codes,
numerical codes ranging from CPT code 00100 to 99499, each of which corresponds
to a specific procedure. 9 The American Medical Association (“AMA”) defines and
updates the CPT codes. 10 The Centers for Medicare and Medicaid (“CMS”) set, and
5 JX 101. 6 Id. at 6, 17–18, 105, 114; PTO ¶ 42. 7 PTO ¶ 44. The current members of the Advisory Group are Brian Farley, Valiance Asset Management Ltd. (“Valiance”), and AMV Partners I, L.P. (“AMV”). Id. Farley was the chair of MyoScience’s board of directors from April 2018 until the merger. Id. ¶ 51. Jan Pensaert is Valiance’s designee and Anthony Lando is AMV’s designee. Id. ¶ 44. The original members of the Advisory Group were Lando, Pensaert, and Timothy Still. Id. Still was MyoScience’s chief executive officer from October 2018 until the merger. Id. ¶ 50. Still left the Advisory Group after he was served as a defendant under the original complaint in this action in August 2020. Id. ¶ 44. 8 Id. ¶ 59. 9 Id. ¶ 60. 10 Id. ¶¶ 4, 19.
3 annually update, how much Medicare—a major insurance provider—will reimburse
health care providers for each CPT-coded procedure. 11 The amount Medicare pays
for a procedure varies depending on the care setting, resulting in different rates in
hospital outpatient, ambulatory surgery center (“ASC”), and physician’s office
settings.12 That, however, is not the only variable.
CMS releases “national” reimbursement rates for each CPT code, but the
national reimbursement rate is not the exact amount a medical professional would
receive from Medicare if reimbursed for the procedure. 13 Care providers are paid
based on a calculation that produces a “locality-adjusted” reimbursement rate that
takes into account the relative cost of care in the geographic location where the
patient is served.14 For example, in 2020, the geographic wage index of different
places across the country ranged from 0.7543 to 1.8551.15 Thus, depending on
where a procedure was performed, the amount that Medicare would reimburse a
medical professional could vary significantly. 16 By contrast, the artificial national
11 Id. ¶ 61; Tr. 15:10–11 (Stack). 12 PTO ¶ 61. 13 “The existence of a CPT code does not guarantee payment of any particular procedure. Payment of any procedure by Medicare is predicated, for example, on the medical necessity of the service and adequate documentation of the procedure.” Id. ¶ 63. 14 Id. ¶ 64. 15 JX 231 ¶ 59. 16 Id. ¶¶ 57–60.
4 reimbursement rate assigned to each CPT code is the dollar value output if all
modifiers in the payment calculation are set to 1. 17 Due to the variability across
different localities, the national reimbursement rate is used in the industry as a
reference point to compare the reimbursement rates for various procedures.18
C. iovera and CPT Codes
iovera is a patented handheld medical device with Class II U.S. Food and Drug
Administration (“FDA”) clearance.19 iovera delivers “intense (extreme) cold via
closed-end needles called ‘Smart Tips’” to targeted locations, temporarily destroying
peripheral nerves and thereby preventing the transmission of pain signals to the
brain.20 The base iovera device is reusable, but the Smart Tip needles that deliver
the cold to the target location are single use. 21
17 Tr. 869:16–870:4 (Yeung). “It is a fictitious, artificial number that provides a useful, shorthand way to compare differences in national rates between different CPT codes.” Def.’s Reply Br. 13. 18 JX 231 ¶¶ 61, 74, 84; see also Tr. 893:4–18 (Yeung) (“Q. And you think that national rates are used in the industry to compare reimbursement for different items and services. Correct? A. That’s correct. I think they can be used to compare different items and services. Q. And national -- you also think national rates can be helpful to compare reimbursement across different sites of service. Correct? A. Correct. Q. And if one didn’t know where a service was being performed, you think that a national rate would be helpful to give a general idea of how that service is reimbursed. Correct? A. The national rate can be helpful, yes, to give a general idea.”). 19 JX 2 at 2; JX 4 at 4. 20 PTO ¶ 70. 21 JX 21 at 5.
5 iovera’s 510(k) clearance from the FDA permits application of the product to
peripheral nerves throughout the body, but makes special note of iovera’s use “for
the relief of pain and symptoms associated with osteoarthritis of the knee for up to
90 days.”22 Indeed, since iovera’s introduction to the market in 2014, it has primarily
been used on the genicular nerves to treat knee pain associated with arthroplasty and
osteoarthritis. 23 MyoScience’s commercial focus was to “own the knee.” 24 This
objective was in large part due to promising data from clinical studies demonstrating
iovera’s efficacy in the knee25 and the large potential market for pain treatment in
the knee.26
22 PTO ¶ 71. iovera’s 510(k) clearance from the FDA provides: The iovera system is used to destroy tissue during surgical procedures by applying freezing cold. It can also be used to produce lesions in the peripheral nervous tissue by the application of cold to the selected site for the blocking of pain. It is also indicated for the relief of pain and symptoms associated with osteoarthritis of the knee for up to 90 days. The iovera system is not indicated for treatment of central nervous system tissue. Id.; see JX 4 at 3, 5. 23 JX 21 at 4. 24 JX 8 at 8, 32, 56. 25 JX 3 at 18–19. The presence of clinical studies and associated data is essential to the commercialization of a medical device or product. Tr. 373:11–374:7 (Kleinhans). 26 Tr. 507:23–508:5 (Farley) (discussing MyoScience’s market penetration into pain treatment for knee-replacement surgery, a procedure performed about a million times each year); see also id. at 11:11–17 (Stack) (“Q: Is there anything in particular about the knee market? A: It’s a large market and -- roughly a million patients a year. And it is very painful. And so, you know, no matter what we do in the marketplace, the pain profile of a total knee arthroplasty is such that it can always be improved.”).
6 Like other medical devices, the commercial success of iovera is heavily
influenced by the reimbursement rates clinicians and health care providers receive
for its use. 27 Prior to the merger, MyoScience saw a large potential market for
iovera, but low CMS reimbursement rates under CPT code 64640.28 Thus,
physicians had to take a loss on a procedure using iovera, which discouraged
widespread adoption.29 Were Medicaid’s reimbursement rates for procedures using
iovera to meet or exceed physicians’ costs, physician demand for iovera, and,
therefore, the value of MyoScience, was expected to increase.30
In May 2018, the AMA announced a new CPT code, then temporarily labeled
as “64xx1,” to report destruction of genicular nerves by a neurolytic agent, which
was expected to take effect in 2020. 31 The application that led to 64xx1 pertained
primarily to a different medical device called “COOLIEF,” which used a targeted
27 Id. at 360:12–24 (Kleinhans); id. at 14:12–15:19 (Stack); id. at 119:8–120:5 (Ellis). 28 Id. at 507:19–508:24, 530:4–15 (Farley). 29 Id. at 508:12–24 (Farley); id. at 530:4–532:2 (Farley) (“Q: [I]t was very difficult for doctors who were using the iovera device in the clinic to turn any sort of profit. Right? A: It would have been the exception, yes. . . . Q: And that factor was hindering adoption of the iovera device in the marketplace? A: We were still growing 100 percent year over year, but we thought we could do better with better reimbursement. . . . Anytime you ask a doctor to not get compensated for their time, and possibly not even have the reimbursement cover the cost of the supply, that would be a headwind.”). 30 Id. at 128:10–14 (Ellis); id. at 22:11–18 (Stack). 31 PTO ¶ 75; see JX 30.
7 application of heat to relieve pain by killing nerves.32 Because the creation of 64xx1
was responsive to an application relating to COOLIEF, which utilized a different
method of treatment and targeted different parts of the knee, there was a risk that
64xx1 would not be applicable to reimburse for iovera. 33 Nevertheless, MyoScience
was hopeful that the new CPT code would cover iovera and took affirmative steps
to influence the parameters of the new CPT code to ensure its applicability to
iovera.34 If the finalized code applied to iovera, it would bode well for MyoScience’s
commercial prospects, as COOLIEF’s higher input costs would be reflected in the
reimbursement rate for CPT code 64xx1. 35 MyoScience learned about this
potentially significantly accretive CPT coding change in May 2018, but the
uncertainty surrounding the scope and reimbursement level of the potential new CPT
code also created challenges in valuing iovera and MyoScience. 36
32 Tr. 511:11–512:14 (Farley); id. at 97:20–98:23 (Stack). 33 Id. at 438:6–9 (Kleinhans); id. at 542:16–543:8 (Farley); JX 65 at 1, 3. 34 Tr. 513:4–16 (Farley); JX 65 at 1 (“There is not much in control [sic] at this point. We will have our attorney present at the upcoming February meeting to make sure our case is appropriately represented and no one provides incorrect information to the committee.”); id. at 1 (Farley responding to the inquiry “how can we increase the number of RVUs for the iovera treatment?” stating that “We can’t. . . . If we tried to influence doctors about this, it would violate the AMA rules . . . .”); id. at 2 (“We’ve already sent in this cost information and it’s been accepted by the RUC.”). 35 Tr. 538:18–539:22 (Farley); JX 65 at 3. 36 While iovera has other uses, there was no immediate prospect for another new CPT code that would be accretive to MyoScience’s value. Applying for a new CPT code requires
8 D. Pacira and MyoScience Explore a Partnership, Then a Merger. In the late summer of 2018, Pacira and MyoScience began discussing a
“possible partnership.” 37 Like MyoScience, Pacira, at the time, sold a single, non-
opioid pain relief product: EXPAREL® (“EXPAREL”), which was FDA approved
for post-surgical acute pain control.38 The effects of iovera and EXPAREL were
complementary,39 and early discussions focused on a co-promotion partnership
proposing a non-opioid pain management protocol 40 and Pacira making an equity
five published papers showing clinical evidence, so when MyoScience was negotiating with Pacira, “[t]here [was] nothing to be done today regarding getting codes for the use of iovera for treatment of other nerve branches” because MyoScience was “quite away from having this.” JX 65 at 2. 37 PTO ¶ 72. 38 Tr. 6:9–24 (Stack); id. at 110:12–18 (Ellis). 39 JX 21 at 4 (“When used in combination, there is an additive effect with a higher likelihood for a completely opioid-free patient journey.”); Tr. 8:6–19 (Stack) (“And so we saw the MyoScience asset as a way to complement the use of EXPAREL. So, you know, use the MyoScience device a couple of weeks to a month before the surgery and allow the patient to undergo what we call ‘prehabilitation,’ start going up and down stairs, get out of the wheelchair, et cetera. You would use EXPAREL, then, for the acute pain of the surgical procedure itself, the total knee arthroplasty. And then that would take you through the acute pain cycle, the three- or four-day cycle. And then you would still benefit from iovera when you went into physical therapy and you had the extended duration of pain based on activity and early ambulation.”). 40 Tr. 11:7–10 (Stack) (“[I]t made sense to be talking to the same clinicians about a protocol of care that would provide additional benefit when used together.”); id. at 376:10–21 (Kleinhans) (“The opportunity to be able to have a protocol was very important to Ron to think about having something that they could have before the surgery with iovera, during the surgery with EXPAREL, after the surgery -- they had just signed a strategic deal -- recently signed a strategic deal with J&J for extra-strength Tylenol. There was this alignment between the strategies of the company to be able to create opioid-free protocols for surgeries. And that was a very powerful message that he was delivering to me and something that resonated with me based on how much I believed in our product.”).
9 investment in MyoScience. 41 The arrangement would provide Pacira an entry-point
into the chronic pain market 42 and allow MyoScience to expand its commercial reach
through Pacira’s well-developed, internal sales force. 43
By December 2018, the proposed structure of the transaction shifted to Pacira
acquiring MyoScience in its entirety. 44 Unsurprisingly, the parties struggled to reach
an agreement on a purchase price.45 They resolved to employ an expanded earnout
mechanism to bridge the gap. 46
On January 2, 2019, Pacira and MyoScience executed a final term sheet,
which contemplated Pacira purchasing 100% of the equity interests in MyoScience
41 JX 21 at 2, 4, 9. 42 Tr. 111:22–112:1 (Ellis) (“The concept is [iovera] could be complementary for Pacira in the knee operative setting as well as offer Pacira an entree into the chronic pain setting.”). 43 Id. at 112:23–113:2 (Ellis); id. at 764:11–16 (Still); id. at 382:3–11 (Kleinhans) (“[Pacira] had a pretty extensive sales force with over 200 sales reps . . . . And so the conversation, as I recall, was they were going to go to their direct sales force to sell our product and to -- as they were selling EXPAREL. And then that we were looking at how we were going to terminate the distributor relationships that we had on our side.”). 44 JX 31. 45 Tr. 766:16–767:1 (Still) (“Q: What was the amount that the board of directors originally demanded from Pacira? A. 225 million. Q. And do you remember what Pacira’s first offer to MyoScience was? A. It was around 140, 145 million. Q. And of that amount, how much was -- was it all -- how was that amount spread out? A. It was about 90 or 95 million was cash up front, and then the balance was on the sales goal.”). 46 Id. at 137:10–16 (Ellis); compare id. at 201:2–5 (Ellis) (“Q: Do you remember roughly how much the first offer was? A: The upfront was less than 100 million, and then 50 sounds right for the milestones.”), with JX 59 at 2–5 (providing, in the final indication of interest, an offer of $120 million in cash up-front and up to an additional $100 million in the earnout), and JX 101 (providing, in the final agreement, $120 million in cash up-front and up to an additional $100 million in the earnout).
10 for up to $220 million, consisting of an upfront payment of $120 million and $100
million in potential milestone payments.47 The term sheet attached half of the value
of the potential milestone payments to three CMS reimbursement-related
milestones.48
E. The Merger Agreement
The parties executed the Merger Agreement on March 4, 2019 49 and
consummated the transaction on April 9, 2019. 50 The upfront purchase price was
$120 million. 51 Thereafter, qualifying former MyoScience stockholders or option
holders (the “Escrow Participants”) were entitled to up to $100 million in contingent
earnout payments (“Milestone Payments”), with $50 million of the Milestone
Payments tied to CMS reimbursement rates (the “CMS Reimbursement
47 PTO ¶ 74; JX 59 at 2–5. 48 PTO ¶ 74; JX 59 at 5. 49 PTO ¶ 77; JX 101. 50 PTO ¶ 79. Section 9.7 of the Merger Agreement provides that: This Agreement and all disputes and controversies arising hereunder will be governed by and construed in accordance with the Laws of the State of Delaware without reference to any jurisdiction’s principles of conflicts of law. Each Party irrevocably consents to the exclusive jurisdiction of and venue in any state or federal court located in the State of Delaware in connection with any matter based upon or arising out of, or with respect to, this Agreement or the matters contemplated herein, and waives and covenants not to assert or plead any objection which such Party might otherwise have to such jurisdiction and venue . . . . JX 101 § 9.7. 51 PTO ¶ 77.
11 Milestones”).52 The Milestone Payments could be achieved between January 1,
2019 and December 31, 2023 (the “Milestone Achievement Period”). 53 Some of the
CMS Reimbursement Milestones were worth more if achieved earlier.54
Specifically, Section 1.15(a)(iv) of the Merger Agreement provides:
(iv) CMS Reimbursement Milestones. Parent will pay the Escrow Participants an amount equal to:
(1) in the case of reimbursement related to use of the Smart Tip Products to treat a patient in the office setting, (A) $20,000,000, if CMS Reimbursement is effective in fiscal year 2020 in an amount equal to or greater than $600.00 per such procedure using such product pursuant to CPT Code 64xx1 (or a different code that is appropriate to describe a procedure in which the Smart Tip Products are used), or in the alternative only, (B) in the event that the condition in subclause (iv)(1)(A) is not met, $10,000,000, if CMS Reimbursement is effective at any time during the Milestone Achievement Period after the end of fiscal year 2020 in an amount equal to or greater than $600.00 per such procedure using such product pursuant to CPT Code 64xx1 (or a different code that is appropriate to describe a procedure in which the Smart Tip Products are used);
(2) in the case of reimbursement related to use of the Smart Tip Products to treat a patient in the ambulatory surgery centers setting, (A) $20,000,000, if CMS Reimbursement is effective in fiscal year 2020 in an amount equal to or greater than $800.00 per such procedure using such product pursuant to CPT Code 64xx1 (or a different code that is appropriate to describe a procedure in which the Smart Tip Products are used), or in the alternative only, (B) in the event that the condition in subclause
52 JX 101 § 1.15(a). 53 Id. § 1.15(b)(i). 54 Compare id. § 1.15(a)(iv)(1)(A), with id. § 1.15(a)(iv)(1)(B); compare id. § 1.15(a)(iv)(2)(A), with id. § 1.15(a)(iv)(2)(B).
12 (iv)(2)(A) is not met, $10,000,000, if CMS Reimbursement is effective at any time during the Milestone Achievement Period after the end of fiscal year 2020 in an amount equal to or greater than $800.00 per such procedure using such product pursuant to CPT Code 64xx1 (or a different code that is appropriate to describe a procedure in which the Smart Tip Products are used); or
(3) in the case of reimbursement related to use of the Smart Tip Products to treat a patient in the out-patient hospital setting, $10,000,000, if CMS Reimbursement is effective at any time during the Milestone Achievement Period in an amount equal to or greater than $1,400.00 per such procedure using such product pursuant to CPT Code 64xx1 (or a different code that is appropriate to describe a procedure in which the Smart Tip Products are used).55
F. Post-Merger Events On July 29, 2019, CMS issued proposed—but not yet final—reimbursement
rates for 2020, including for CPT code 64xx1. 56 Pacira reviewed the preliminary
national reimbursement rates for CPT code 64xx1 and stated that, based on the
proposed reimbursement rates, there was “no iovera milestone triggered.”57
Internally, Still expressed that he “want[ed] to make sure that Pacira is not missing
anything here that will wind up costing myoscience shareholders 3 milestones based
55 PTO ¶ 78; JX 101 § 1.15(a)(iv). 56 PTO ¶ 80. 57 Id.; JX 125 at 2; Tr. 172:8–173:9 (Ellis) (explaining that the reimbursement rates identified in JX 125 “reflect the national reimbursement for the proposed CPT code 64xx1 by the three sites of care”).
13 on proposed rates.”58 To improve the chances that the reimbursement rates for CPT
code 64xx1 would be increased, Still sought to re-engage Gail Daubert, a
reimbursement attorney who had worked with MyoScience in the past. 59 Still also
told Dave Stack, Pacira’s chief executive officer and board chair, that the
preliminary rates were “fraught with misinformation and miscalculations,” and
offered his “assistance” to Pacira to “correct the misinformation / miscalculations.”60
Fortis, through counsel, sent a letter to Pacira contending that Pacira was
unreasonably delaying in its efforts to increase the value of 64xx1,61 and former
MyoScience securityholders expressed concern internally. 62 On September 13,
2019, Pacira “urg[ed] CMS to revise the proposed valuation of new CPT code
64xx1,” which by then was identified as 64624.63
CMS issued the final 2020 reimbursement rates in November 2019.64
Internally, Pacira identified the final 2020 national reimbursement rates for CPT
58 JX 130 at 2. 59 Id. at 1–3; JX 47. 60 JX 135 at 3–4; PTO ¶ 46. 61 JX 137. This letter was approved by the Advisory Group. JX 136; Tr. 807:21–809:14 (Still). 62 See, e.g., JX 138 at 1. 63 JX 140 at 1. 64 PTO ¶ 81. The new CPT code 64624 was described as “destruction by neurolytic agent, genicular nerve branches including imaging guidance, when performed.” Id. ¶ 83; see JX
14 code 64624 as $417.56 for the physician office setting, $471.33 for the ASC setting,
and $1,871.82 for the hospital outpatient setting.65 Based on these rates, Pacira
determined that the CMS Reimbursement Milestone for the hospital outpatient
setting had been met.66 On January 13, 2020, Pacira notified Fortis that the CMS
Reimbursement Milestone for the hospital outpatient setting had been triggered,67
and, on or about May 22, 2020, Pacira paid that milestone.68
Fortis appears to have initially believed that the CMS Reimbursement
Milestones for the ASC and physician office settings had not been met. On January
8, 2020, Still sent an email to the other members of the Advisory Group, stating:
“[W]e have achieved the Hospital Reimbursement Milestone from CMS for 2020.
The clinic and ASC Milestones were not achieved in 2020; however, we still have
until 2023 to achieve partial payment.”69 The email attached a presentation that
listed the national reimbursement rates for CPT codes 64640 and 64624. 70 The only
145 at 3. The description also includes a parenthetical stating that “64624 requires the destruction of each of the following genicular nerve branches: superolateral, superomedial, and inferomedial. If a neurolytic agent for the purposes of destruction is not applied to all of these nerve branches, report 64624 with modifier 52.” PTO ¶ 83; see JX 145 at 7. 65 JX 145 at 5; JX 146 at 2. PTO ¶ 81; JX 143. A reimbursement rate of at least $1,400 was required to trigger the 66
CMS Reimbursement Milestone for the hospital outpatient setting. JX 101 § 1.15(a)(iv)(3). 67 PTO ¶ 85; JX 161. 68 PTO ¶ 86. 69 JX 159 at 1. 70 Id. at 5–8.
15 immediate concern raised by any member of the Advisory Group or individual at
Fortis upon Pacira’s notification was Still’s admonition that payment for the hospital
outpatient milestone should be made sooner.71
A few months later, Fortis took a more aggressive approach. On May 29,
2020, after Pacira made the hospital outpatient milestone payment, Fortis sent a letter
to Pacira asserting that the CMS Reimbursement Milestones in the ASC and
physician office settings had been met under the final 2020 CMS reimbursement
rates. 72 Fortis pointed to several CPT codes other than 64640 and 64624 and
contended that locality-adjusted rates or combination billing yielded rates in excess
of the payment threshold for the outstanding milestones.73
G. Procedural History On August 21, 2020, Plaintiffs commenced this action, filing claims against
Fortis and various individual defendants. 74 On October 5, 2020, Fortis filed a partial
71 JX 162 at 1. 72 PTO ¶ 87; JX 192. 73 JX 192. Fortis has since modified the list and combinations of CPT codes it believes entitle the Escrow Participants to the Milestone Payments for the CMS Reimbursement Milestones in the ASC and physician office settings. Compare id., with Def.’s Answering & Opening Br. 24–25. 74 Dkt. 1. The individual defendants were Still, Gumballa Kris Kumar, and Jessica Preciado. Dkt. 1. Kumar was MyoScience’s head of product management and marketing at the time of the merger. PTO ¶ 54. Post-merger, Kumar worked as a consultant for Pacira for approximately six months. Id. Preciado was MyoScience’s director of clinical operations at the time of the merger. Id. ¶ 53. Post-merger, Preciado worked at Pacira in various capacities until August 2020. Id.
16 motion to dismiss, submitted an answer, and asserted a counterclaim against
Pacira.75 That same day, the individual defendants moved to dismiss all claims
against them. 76 On October 25, 2021, the court granted both motions to dismiss in
their entirety, with the only remaining claims being Plaintiffs’ claim for declaratory
judgment and Defendant’s mirror-image counterclaim for breach of contract. 77
As trial approached, the parties collectively filed four motions in limine, two
of which warrant discussion. Plaintiffs indicated that they intended to introduce
evidence and argument regarding reimbursement for and usage of specific CPT
codes with iovera. Defendant contended that Plaintiffs sprung this theory on
Defendant on the eve of trial and failed to put Defendant on notice of this theory
during fact discovery. In response, Defendant moved to exclude all argument and
evidence regarding reimbursement and usage. 78 Defendant did not request a remedy
other than the wholesale exclusion of all evidence and argument on the subjects, but
did proffer Andrea Trescot, M.D. as a fact witness on the subject shortly before trial,
should Defendant’s motion in limine fail. Plaintiffs opposed Defendant’s motion,
contending that reimbursement and usage were relevant and that Plaintiffs had put
75 Dkts. 12–13. 76 Dkt. 14. 77 Dkt. 56. 78 Dkt. 122; Dkt. 143 ¶¶ 7–8.
17 Defendant on notice of the theory earlier in the case. 79 Separately, Plaintiffs sought
to exclude Trescot’s testimony on the grounds that Defendant did not identify
Trescot until after the close of fact discovery.80 The court denied both motions,
allowing argument and evidence on reimbursement and usage and permitting
Trescot to testify as a fact witness at trial. 81 The court held trial from September 19
to 21, 2023, and, after briefing, heard post-trial argument on March 11, 2024.82
II. ANALYSIS The parties dispute only whether the conditions precedent set forth in Sections
1.15(a)(iv)(1)(A), 1.15(a)(iv)(1)(B), and 1.15(a)(iv)(2)(A) of the Merger Agreement
have been satisfied (the “Disputed Milestones”). Defendant contends that the
Disputed Milestones were triggered in 2020 by locality-adjusted reimbursement
rates for CPT codes 64600, 64640, and 64681, and by local or national
79 Dkt. 136. 80 Dkt. 123. 81 Dkt. 177 at 54:22–56:9, 56:24–57:11; Dkts. 170–71. 82 Dkts. 178, 184, 189, 191, 193, 195. During the pendency of this action, CMS issued new reimbursement rates, effective January 1, 2021. The 2021 national reimbursement rates for CPT code 64624 in the hospital outpatient, ASC, and physician office settings were $1,754.39, $804.72, and $424.65, respectively. JX 231 at 26–27. On January 18, 2021, Pacira notified Fortis that the CMS Reimbursement Milestone for the ASC setting had been met for calendar year 2021 and confirmed that Pacira would pay $10 million, less any applicable deductions and withholdings. PTO ¶ 91; JX 207. Pacira made that milestone payment on May 28, 2021. PTO ¶ 92.
18 reimbursement rates for CPT codes 64605 and 64610.83 Plaintiffs argue that only
national reimbursement rates for CPT code 64624 can trigger the Disputed
Milestones and that, in any event, iovera must have been used for a procedure
described by the triggering CPT code. The dispositive disputes can be distilled into
two questions. First, must one look to the “national” or “locality-adjusted”
reimbursement rate to determine whether a Disputed Milestone was triggered?
Second, which CPT codes can trigger the Disputed Milestones? The resolution of
these questions is the province of well-settled principles of contract interpretation.
A. Standard of Review
The Declaratory Judgment Act authorizes Delaware courts to “declare rights,
status and other legal relations whether or not further relief is or could be claimed.”
10 Del. C. § 6501. A party “may have determined any question of construction or
validity arising under [a] contract . . . and obtain a declaration of rights, status or
other legal relations thereunder.” Id. § 6502. Plaintiffs seek a declaration that no
sums are owed under the Disputed Milestones. Defendant’s counterclaim is the
other side of the coin; Defendant argues that Pacira breached the Merger Agreement
by failing to make payments under the Disputed Milestones.
83 See Def.’s Answering & Opening Br. 24–25. For some of these codes, Defendant also adds the value of CPT code 76942 or counts the value of the code multiple times, but while the parties spar over the propriety of each of those approaches as well, the court need not reach these issues.
19 Neither party disputes that the Merger Agreement is a valid and binding
contract,84 and neither party contests the calculation of the remedy the other seeks.
The sole dispute is the proper construction of the Merger Agreement. 85
“The proper construction of any contract . . . is purely a question of law.”
Rhone-Poulenc Basic Chems. Co. v. Am. Motorists Ins. Co., 616 A.2d 1192, 1195
(Del. 1992). The court must review the Merger Agreement using the well-
established principles of contract construction to ascertain what the parties intended.
See GreenStar IH Rep, LLC v. Tutor Perini Corp., 2017 WL 5035567, at *6 (Del.
Ch. Oct. 31, 2017) (interpreting an earnout provision in a merger agreement and
explaining that the court is “bound by the language within the contract unless that
language is ambiguous” and that “the role of a court . . . is to effectuate the parties’
intent” (internal quotation marks omitted)), aff’d, 186 A.3d 799 (Del. 2018)
(TABLE).
In reviewing merger agreements and other contracts, Delaware courts
“adhere[] to the ‘objective’ theory of contracts, i.e. a contract’s construction should
be that which would be understood by an objective, reasonable third party.” Osborn
ex rel. Osborn v. Kemp, 991 A.2d 1153, 1159 (Del. 2010) (internal quotation marks
84 Dkt. 1 ¶ 260; Dkt. 12 at 123. 85 While the burden may vary between the parties’ respective claims, see State Farm Mutual Automobile Insurance Co. v. Spine Care Delaware, LLC, 238 A.3d 850, 860 n.55 (Del. 2020), the evidence here is not in equipoise, so who bears the burden is immaterial.
20 omitted). The court must read the contract “as a whole and enforce the plain
meaning of clear and unambiguous language.” Manti Hldgs., LLC v. Authentix Acq.
Co., 261 A.3d 1199, 1208 (Del. 2021). If the contractual language is clear, the court
“will give priority to the parties’ intentions as reflected in the four corners of the
agreement, construing the agreement as a whole and giving effect to all its
provisions.” In re Viking Pump, Inc., 148 A.3d 633, 648 (Del. 2016) (internal
quotation marks omitted). Contractual language is clear “[w]hen the plain, common,
and ordinary meaning of the words lends itself to only one reasonable
interpretation.” Sassano v. CIBC World Mkts. Corp., 948 A.2d 453, 462 (Del. Ch.
2008).
If a contract’s language is ambiguous, then the court must look to other
sources to determine what an objectively reasonable third party would have
understood the parties’ intent to be. United Rentals, Inc. v. RAM Hldgs., Inc., 937
A.2d 810, 834–35 (Del. Ch. 2007). “A contract is not rendered ambiguous simply
because the parties do not agree upon its proper construction. Rather, a contract is
ambiguous only when the provisions in controversy are reasonably or fairly
susceptible of different interpretations or may have two or more different meanings.”
Rhone-Poulenc, 616 A.2d at 1196. Nor is a contract unambiguous simply because
both sides contend that its meaning is plain. See Sunline Com. Carriers, Inc. v.
CITGO Petroleum Corp., 206 A.3d 836, 847 n.68 (Del. 2019) (explaining that
21 “whether a contract is unambiguous is a question of law; this Court cannot find an
ambiguous contract unambiguous because each party interprets the contract
differently to find it unambiguous”). Ambiguity exists if “the provisions in
controversy are fairly susceptible of different interpretations.” Eagle Indus., Inc. v.
DeVilbiss Health Care, Inc., 702 A.2d 1228, 1232 (Del. 1997). “The determination
of ambiguity lies within the sole province of the court.” Osborn, 991 A.2d at 1160.
“[T]he introduction of extrinsic, parol evidence does not alter or deviate from
Delaware’s adherence to the objective theory of contracts”; rather, “the extrinsic
evidence may render an ambiguous contract clear so that an ‘objectively reasonable
party in the position of either bargainer would have understood the nature of the
contractual rights and duties to be.’” United Rentals, 937 A.2d at 835 (quoting U.S.
W., Inc. v. Time Warner Inc., 1996 WL 307445, at *10 (Del. Ch. June 6, 1996)).
The crux of the parties’ dispute is whether the Disputed Milestones were
triggered, thus requiring Pacira to make the corresponding payments. The parties’
claims turn on two determinations: (1) whether “CMS Reimbursement” rate refers
to the national or locality-adjusted reimbursement rates, and (2) whether “a different
code that is appropriate to describe a procedure in which the Smart Tip Products are
used” encompasses all CPT codes that could theoretically be used to reimburse for
iovera. The starting point for each of these inquiries is the Merger Agreement and
the words that the contracting parties chose to govern their rights and obligations.
22 B. The Defined Term “CMS Reimbursement” is Ambiguous, but the Extrinsic Evidence Demonstrates that the Parties Intended the Disputed Milestones to Be Triggered by the National Reimbursement Rate.
The parties’ first dispute concerns whether the “national” or a “locality-
adjusted” reimbursement rate is the appropriate metric for determining whether
reimbursement for a given CPT code exceeds a milestone threshold.
1. The plain language of the Disputed Milestones regarding the reimbursement rate is ambiguous.
The court starts with the plain language of the Disputed Milestones, which
provides that “[Pacira] will pay . . . if the CMS Reimbursement is effective . . . in an
amount equal to or greater than [$600.00/$800.00] per such procedure . . . .” 86 In
turn, the Merger Agreement defines “CMS Reimbursement” as “the reimbursement
scheme authorized and approved by the Centers for Medicare & Medicaid Services
for the relevant procedure that involves the use of the Company product.” 87 The
court must determine the “amount” at which the CMS “reimbursement scheme” is
“effective” for a procedure related to the use of iovera to determine if the Disputed
Milestones are owed. The key dispute here is over the meaning of “reimbursement
scheme.”
86 JX 101 §§ 1.15(a)(iv)(1)–(2). Aside from the threshold amounts and site of service, the relevant language is substantively identical for each of the Disputed Milestones. 87 Id. at 101.
23 Defendant argues that “reimbursement scheme” refers to the locality-adjusted
reimbursement rates because that is what a medical care provider gets paid, prior to
any reductions. Defendant contends that the “scheme” refers to the system of
locality-adjusted reimbursement rates with respect to each CPT code, not the
generalized benchmark national rates. In sum, Defendant argues that the language
requires payment if, pursuant to the scheme for geographic adjustment calculations,
any single locality-adjusted reimbursement rate for a relevant code exceeds the
payment threshold.
By contrast, Plaintiffs contend that “reimbursement scheme” refers to the
broader system of national reimbursement rates promulgated by CMS, and that the
national rate for a relevant CPT code is the correct metric. In other words, Plaintiffs
argue that the language requires payment only if, under CMS’s scheme of national
benchmark reimbursement rates, the national rate for a relevant code exceeds the
The parties advance only these two metrics, and no other value against which
to measure the Disputed Milestones is compelled by the Merger Agreement’s plain
language. Neither interpretation is especially compelling based only on the language
in the Merger Agreement, but both are metrics from which one can determine an
“effective” “amount,” and each plays a significant role in a “reimbursement
24 Each side advances a slew of arguments as to why its construction is the only
reasonable one, but neither party can muster a conclusive refutation of the other’s
interpretation. Neither side finds specific language in the Merger Agreement to
bolster their own interpretation or to undermine the other side’s construction. The
defined term “CMS Reimbursement” is used only in the CMS Reimbursement
Milestones; there is no other reference to CMS in the Merger Agreement and neither
side proffers support for its interpretation from other language in the four corners of
the contract. Nor does the concept of a national or locality-adjusted reimbursement
rate appear in the pertinent language or draw direct support from words used
elsewhere in the agreement. Both parties’ interpretations can be reasonably traced
to the broad, sparse language in Section 1.15(a) and the definition of CMS
Reimbursement, but neither interpretation finds strong enough foothold to firmly
displace the other. Rather, the words on the page of the Merger Agreement leave
plenty of room for both interpretations. Finally, each party offers arguments as to
why the other’s interpretation might be unnatural or ill-advised. For example,
Defendant highlights that the national reimbursement rate is “a fictional number, not
a reimbursement payment value,”88 and Plaintiffs contend that “monitoring
hundreds of locality-adjusted rates across three sites of service over four years would
88 Def.’s Answering & Opening Br. 38.
25 be a massive burden that no rational party would have (tacitly) agreed to
undertake.”89 But the national rate does not need to be an actual reimbursement
payment value to serve as a metric for an earnout, and Plaintiffs’ hyperbole about
the “burden” of occasionally multiplying the highest locality modifiers against the
handful of potentially applicable code inputs is unpersuasive. Neither side convinces
the court that the other’s construction “produces an absurd result or one that no
reasonable person would have accepted when entering the contract.” Osborn, 991
A.2d at 1160.
When faced with two reasonable interpretations of a contract, the court does
not simply end the inquiry by deciding which of two reasonable interpretations is
“more” reasonable. Terrell v. Kiromic Biopharma, Inc., No. 131, 2024, slip op. at
12 (Del. Jan. 21, 2025) (explaining that a “trial court cannot choose between two
reasonable interpretations of an ambiguous contract” as a matter of law); Bank of
N.Y. Mellon v. Commerzbank Cap. Funding Tr. II, 65 A.3d 539, 550 (Del. 2013)
(“Although the more natural reading is a factor to be considered, it does not conclude
the analysis. Even a less natural reading of a contract term may be reasonable for
purposes of an ambiguity inquiry.” (cleaned up)); AM Gen. Hldgs. LLC v. Renco
Gp., Inc., 2017 WL 2167193, at *2 n.8 (Del. Ch. May 17, 2017) (“Even if the Court
89 Pls.’ Reply & Answering Br. 13.
26 determines that one party’s reading of the contract is more reasonable or ‘natural,’
that does not preclude a finding of ambiguity.”), reargument denied, 2017 WL
3046819 (Del. Ch. July 18, 2017); Cities Serv. Co. v. Gardinier, Inc., 344 A.2d 254,
259 n.7 (Del. Super. 1975) (denying summary judgment despite one side having
acknowledged that the other’s interpretation was “the more reasonable among the
two possible interpretations arising out of the ambiguity,” explaining that “extrinsic
evidence may, in fact, demonstrate” that the parties agreed to the second,
nevertheless reasonable interpretation), appeal refused, 349 A.2d 744 (Del. 1975).
The court’s role in interpreting a contract is to give effect to the parties’ intent.
The parties’ intent is the central focus, and if the court cannot determine the parties’
intent from the agreement’s language, the court turns to the extrinsic evidence. See
United Rentals, 937 A.2d at 835 (explaining that “the extrinsic evidence may render
an ambiguous contract clear”); see also Martin Marietta Mat’ls, Inc. v. Vulcan
Mat’ls Co., 56 A.3d 1072, 1105–06 (Del. Ch. 2012) (observing that the court first
looks to “the plain and unambiguous terms of a contract as the binding expression
of the parties’ intent” but “if words in the contract are ambiguous, then [the court]
must look to extrinsic evidence to determine the parties’ intent”), aff’d, 45 A.3d 148
(Del. 2012) (TABLE), and aff’d, 68 A.3d 1208 (Del. 2012), as corrected (July 12,
2012).
27 This is the course the court must follow here to determine what the parties
meant by “CMS Reimbursement.” Both interpretations point to metrics that fall
within the un-specific language at issue and are reasonable interpretations of the
Disputed Milestones. The ambiguity or uncertainty in issue is plainly discernable
from a reading of the Merger Agreement without consideration of any extrinsic
evidence. Therefore, the Merger Agreement is ambiguous as to the appropriate
metric, and the court must turn to extrinsic evidence to determine the parties’ shared
intent at the time of contracting.
2. The extrinsic evidence demonstrates that the parties intended to tie the Disputed Milestones to a national reimbursement rate. The extrinsic evidence overwhelmingly indicates that the parties’ shared
intent at the time of the Merger Agreement was for the national reimbursement rates
to serve as the relevant metric. First, the parties discussed national reimbursement
rates throughout their negotiations, but never discussed that the thresholds in the
CMS Reimbursement Milestones could be triggered by locality-adjusted
reimbursement rates.90 For example, MyoScience’s presentations to Pacira in
October 2018 and January 2019 provided only the national reimbursement rates for
90 See, e.g., Tr. 600:16–601:10 (Farley) (explaining that MyoScience only looked at the national reimbursement rates when analyzing the potential reimbursement rates that would apply for CPT code 64xx1).
28 CPT code 64640 in the hospital outpatient, ASC, and physician office settings.91
Ron Ellis, Pacira’s chief strategy officer, testified that he understood that the
reimbursement rates discussed by the parties were the national reimbursement
rates. 92 No one from MyoScience looked into any locality-adjusted reimbursement
rates during the parties’ negotiations, 93 and Stack was not even aware that locality-
adjusted reimbursement rates existed for medical devices.94 The pre-merger
evidence alone supports a finding that both parties understood and intended for the
Disputed Milestones to be triggered, if at all, by the national reimbursement rates.
Second, evidence from after the Merger Agreement’s execution further
confirms that the parties had intended for the national reimbursement rates to serve
as the relevant metric.95 As CMS announced the proposed and finalized
91 JX 24 (native) at 50 (October 24, 2018 presentation listing national reimbursement rates for the three sites of service); Tr. 126:1–4 (Ellis) (confirming the reimbursement rates in the October 24, 2018 presentation were the national rates); JX 66 at 5 (January 9, 2019 presentation listing national reimbursement rates for the three sites of service). 92 Tr. 139:17–23 (Ellis); PTO ¶ 45. 93 Pensaert Dep. at 219:13–22. 94 Tr. 32:14–33:3 (Stack) (explaining that his “prior experience was in pharmaceuticals. And I was aware that that would be common practice in pharmaceuticals, but I didn’t have any previous device experience. And so I did not understand that, no.”). 95 Defendant broadly avers to the following language in Section 9.2 of the Merger Agreement: No prior draft of this Agreement nor any course of performance or course of dealing shall be used in the interpretation or construction of this Agreement. No parole evidence shall be introduced in the construction or interpretation
29 reimbursement rates in July and November 2019, the parties’ correspondence
between each other and internally reflected only the national reimbursement rates.96
of this Agreement unless the ambiguity or uncertainty in issue is plainly discernable from a reading of this Agreement without consideration of any extrinsic evidence. JX 101 § 9.2. Through this language, the parties to the Merger Agreement permissibly agreed that prior drafts, course of performance, and course of dealing would not be used to interpret or construe the Merger Agreement. See Tex. Pac. Land Corp. v. Horizon Kinetics LLC, 306 A.3d 530, 552–53 (Del. Ch. 2023) (“The No Drafting History Clause is a rational way for parties to address known risks. . . . Ambiguity is a known risk, and parties can contract to address that risk. . . . Enforcing the clause also seems warranted because it does not unduly burden the court’s ability to consider relevant evidence. It allows the parties to agree on what evidence is relevant.”), aff’d, 314 A.3d 685 (Del. 2024) (TABLE). Section 9.2 also recites Delaware’s well-established rule regarding extrinsic evidence. See Cox Commc’ns, Inc. v. T-Mobile US, Inc., 273 A.3d 752, 760 (Del. 2022) (“We do not consider extrinsic evidence unless we find that the text is ambiguous.”), reargument denied (Mar. 22, 2022). For the avoidance of doubt, the court does not consider the parties’ prior drafts in interpreting the Merger Agreement. Nor does the court consider the parties’ course of performance which, here, amounts to Pacira’s payment and Fortis’s acceptance of the two undisputed Milestone Payments. See Motors Liquid. Co., Dip Lenders Tr. v. Allianz Ins. Co., 2013 WL 7095859, at *5 (Del. Super. Dec. 31, 2013) (“Course of performance is a sequence of conduct where: (1) the agreement of the parties involves repeated occasions for performance by a party; and (2) the other party knowingly accepts the performance or acquiesces in it without objection.”), aff’d, 191 A.3d 1109 (Del. 2018) (TABLE). Finally, the parties here have no course of dealing to consider. See Restatement (Second) of Contracts § 223 (Am. L. Inst. 1981) [hereinafter “Restatement (Second) of Contracts”] (“A course of dealing is a sequence of previous conduct between the parties to an agreement which is fairly to be regarded as establishing a common basis of understanding for interpreting their expressions and other conduct.”). 96 In July 2019, CMS issued proposed reimbursement rates for 2020. Pacira reviewed only the proposed national reimbursement rates for CPT code 64xx1 and determined that “no iovera milestone [was] triggered.” JX 125 at 2; Tr. 172:8–173:9 (Ellis) (explaining that the reimbursement rates identified in JX 125 “reflect the national reimbursement for the proposed CPT code 64xx1 by the three sites of care”). The internal Pacira email was forwarded to Still, who then forwarded it to Daubert and Farley. JX 126 at 1–3. None of
30 For months, former MyoScience securityholders’ only concerns were that Pacira
might not be effectively advocating for rate increases and that Pacira’s proposed
payment timeline was slow.97 In reaction to the finalized national reimbursement
rates, MyoScience’s former chief executive officer lamented that, based on the
them discussed the possibility that the locality-adjusted reimbursement rates should be considered. In November 2019, again referring only to the national reimbursement rates for CPT code 64624 (the finalized version of 64xx1), Ellis told Stack that “it now appears that CMS granted a healthy increase in [the hospital outpatient setting], triggering a $10M milestone payment.” JX 150 at 1, 4; see Tr. 176:15–177:5 (Ellis); see also JX 143 at 1. In the months following the November 2019 rate announcements, MyoScience securityholders and their representatives consistently indicated that they believed that they had missed the Disputed Milestones based on the national reimbursement rate. Between November 2019 and January 2020, Still repeatedly told Fortis and other MyoScience securityholders that only the hospital outpatient milestone had been met and that the ASC and physician office milestones had not been met. JX 153 at 1 (November 26, 2019 email from Still to Lando stating that it “looks good for CMS milestone for hospital; Clinic is close; ASC won’t happen for 2020”); JX 159 at 1, 3–8 (January 8, 2020 email from Still forwarding Pacira’s presentation showing only the national reimbursement rates for CPT codes 64640 and 64624 to Fortis and the Advisory Group, stating: “You will see from the attached that we have achieved the Hospital Reimbursement Milestone from CMS for 2020. The clinic and ASC milestones were not achieved in 2020; however, we still have until 2023 to achieve partial payment.”); JX 163 at 1 (January 22, 2020 email from Still to Andrew Jones, MyoScience’s vice president of finance, stating that the CMS reimbursement rate for the physician office setting was “$26 dollars short for 2020.... wound up costing us $10M”). In January 2020, Kumar stated to Still: “Unfortunately, we did not trigger the milestone for clinic payment,” citing only the “nat’l avg” for CPT code 64624. JX 159 at 2. 97 See, e.g., JX 162 at 1 (discussing former MyoScience securityholders’ desire for earlier payment and basis for contending that the hospital outpatient milestone should be paid at the end of February, rather than waiting until June 1); JX 138 at 1 (email from Pensaert to Valiance stating that “we will need to monitor closely whether Pacira is making all reasonable efforts to obtain the reimbursement levels as agreed, which risks delaying reimbursement until 2021” and thus “reduc[ing] the potential CMS Reimbursement Milestone . . . from a total of $50,000,000 to $30,000,000”).
31 national reimbursement rate for 64640, “we were a mere $24.00 short.”98 Both pre-
merger and post-merger evidence confirms Plaintiffs’ interpretation.
Where, then, did the locality-adjusted reimbursement rate theory originate?
Plaintiffs persuasively showed that a consultant devised the theory in the spring of
2020. 99 When the consultant first proposed the concept, Farley expressed skepticism
as to its viability, emailing Still his concerns that “[i]t’s unclear from this
presentation how we hope to use the argument that in certain locations such as Santa
Clara county, the $600 milestone threshold is achieved.” 100 Still explained that “We
will try to argue that our milestone has been met - even though national average is
light.... We’ll see :).”101 To Defendant’s credit, its consultant proffered a reasonable
interpretation of the relevant language. But proffering a reasonable interpretation of
ambiguous language cannot, alone, carry the day. Defendant’s attempt to show that
the parties intended to use the locality-adjusted reimbursement rates falls apart once
the court reaches the extrinsic evidence, which shows that Defendant’s position lacks
support in the record.
Based on the extrinsic evidence, the court finds that the parties’ shared
understanding at the time of contracting was that the Disputed Milestones could be
98 JX 169 at 1. 99 See JX 173; JX 174; JX 178; JX 184; JX 183. 100 JX 183 at 1. 101 Id.
32 triggered only if the national reimbursement rate for certain CPT codes exceeded the
threshold for the relevant care settings. This is not, however, the end of the inquiry.
The court must now decide whether and the extent to which the Disputed Milestones
can be triggered by reimbursement rates for CPT codes other than 64624.
C. The Disputed Milestones Can Be Triggered by Any CPT Code Appropriate to Describe a Procedure for Which iovera Is Actually Used, but Defendant Has Not Shown that the Reimbursement Rate for Any Other Applicable Code Exceeded the Threshold for Payment.
The parties next dispute whether the Disputed Milestones can be triggered by
CPT codes other than 64xx1, as finalized. Plaintiffs contend that the unambiguous
language of the Merger Agreement provides that 64624 is the only CPT code that
can trigger the Disputed Milestones. Defendant contends that other CPT codes can
trigger the Disputed Milestones.
1. CPT codes other than 64624 can trigger the Disputed Milestones but iovera must have actually been used for a procedure appropriately described by such CPT code.
The pertinent language from the Merger Agreement provides for payment of
each Disputed Milestone:
[I]n the case of reimbursement related to use of the Smart Tip Products to treat a patient in [a given care] setting, [] if CMS Reimbursement is effective [] in an amount equal to or greater than [$600.00/$800.00] per such procedure using such product pursuant to CPT Code 64xx1 (or a different code that is appropriate to describe a procedure in which the Smart Tip Products are used).102
102 JX 101 §§ 1.15(a)(iv)(1)–(2).
33 Plaintiffs contend that, under this language, the Disputed Milestones can only
be triggered by reimbursement rates for CPT code 64624 that exceed the specified
threshold amount. Defendant argues that the phrase “or a different code”
unambiguously provides that CPT codes other than 64xx1 can trigger the Disputed
Milestones, highlighting that nothing in the Disputed Milestones indicates that the
parenthetical modifies 64xx1. Plaintiffs counter that the parenthetical serves only to
modify “64xx1” to address what Plaintiffs argue is the risk that 64xx1 would be
finalized in another family of codes. Not so.
“64xx1” referred to what was, at the time of the Merger Agreement, a
provisional, yet-to-be-finalized CPT code. And there is precedent for CPT codes
being finalized in “code families” other than their provisional code.103 But once
finalized, regardless of what the final number ended up being, which CPT code had
been finalized from 64xx1 would be objectively verifiable.104 Therefore, reference
103 Tr. 278:11–279:20 (Kahan) (explaining that placeholder code 37x01 had been finalized as CPT code 30469, in a different “family” of codes). 104 Even if a placeholder code is finalized in a different family of codes, the federal register provides information in an appendix to the final rule with which one can identify the final CPT code’s placeholder predecessor. Id. at 278:11–279:20 (Kahan) (“A: “[W]e know that [30469] was the code that was finalized from the [37x01] placeholder code because the federal register gives us that information in an appendix to their final rule. Q: So this is all publicly available information? A: It is.”).
34 to “CPT Code 64xx1” in a merger agreement dated March 4, 2019,105 was sufficient
to identify the finalized code in 2020. Plaintiffs’ interpretation, therefore, renders
the entire parenthetical surplusage. See NAMA Hldgs., LLC v. World Mkt. Ctr.
Venture, LLC, 948 A.2d 411, 419 (Del. Ch. 2007) (“Contractual interpretation
operates under the assumption that the parties never include superfluous verbiage in
their agreement, and that each word should be given meaning and effect by the
court.”), aff’d, 945 A.2d 594 (Del. 2008) (TABLE).
Construing the parenthetical to refer to CPT codes other than 64624 gives that
language meaning. Plaintiffs insist, however, that reading the parenthetical to
include other CPT codes renders “64xx1” meaningless surplusage. It does not, for
at least two reasons.
First, Defendant’s interpretation creates two categories of CPT codes for
potential Milestone Payments: 64xx1 or a “different” code. 64xx1 is not a different
code from 64xx1. Therefore, Plaintiffs’ argument boils down to, essentially, a
complaint that Defendant’s interpretation could have been said in fewer words.106
But concision, though a virtue, is not a principle of contract interpretation.
105 64xx1, like other placeholder codes, can be, and actually was, reused after CPT code 64624 was finalized. See JX 231 ¶ 37. Placeholder codes are, however, only reused once the first proposed codes are finalized, so, on March 4, 2019—the date of the Merger Agreement—there was only one “64xx1.” See id. ¶¶ 36–38 (explaining that a placeholder code is only given a permanent CPT code number once the application is accepted and showing that the placeholder code “64xx1” was not reused until 2022). 106 In Plaintiffs’ words, “why single out 64xx1 at all?” Pls.’ Opening Br. 21.
35 Second, under the plain language of the Merger Agreement, 64xx1 and
“different” codes are not treated the same for purposes of determining whether a
Disputed Milestone is achieved. The main phrase requires only that CMS
reimbursement be “effective” for 64xx1. By contrast, the parenthetical requires that
“different” codes describe a procedure in which the Smart Tip Products (i.e., iovera)
“are used.”
A version of the word “use” appears in the relevant provisions three times:
first, in the opening clause, “in the case of reimbursement related to use of the Smart
Tip Products to treat a patient in [a given] setting”; second, in the core of the main
clause, “per such procedure using such product pursuant to”; and third, in the
parenthetical, “code that is appropriate to describe a procedure in which the Smart
Tip Products are used.” 107 The second instance falls within a phrase referring back
to the first (“such procedure using such product”). Thus, there are, in effect, two
constructions, which differ materially in structure. Compare (“in the case of
reimbursement related to use of the Smart Tip Products to treat a patient in [a given
setting]”), with (“a procedure in which the Smart Tip Products are used”). If the
parenthetical were intended to have the same meaning, the drafters knew how to
employ phrasing to do so. They did not; therefore, it is reasonable to conclude that
107 JX 101 §§ 1.15(a)(iv)(1)–(2).
36 they intended another meaning—and one is plainly apparent. The first instance
contemplates hypothetical use; “in the case of reimbursement related to use”
indicates that the milestone does not, necessarily, require actual use. See City of
Newark v. Donald M. Durkin Contr., Inc., 305 A.3d 674, 680 (Del. 2023)
(“Delaware courts recognize the phrases ‘relating to’ and ‘arising out of’ as
‘paradigmatically broad terms.’” (quoting Lillis v. AT & T Corp., 904 A.2d 325, 331
(Del. Ch. 2006))). By contrast, the parenthetical uses direct language requiring
actual use, referring to “a procedure in which the Smart Tip Products are used.”
Moreover, were the language in the parenthetical not intended to provide “different”
codes with different treatment than 64xx1, all of the parenthetical other than “or a
different code” would be surplusage, as prior language in each Disputed Milestone
already specifies that any triggering code pertains to reimbursement related to use
of iovera in the specified setting. Therefore, construing 64xx1 as not requiring actual
use and “different” codes as requiring actual use to trigger a Disputed Milestone
affords full meaning not only to “or a different code” but also the rest of the
parenthetical. See Manti Hldgs., 261 A.3d at 1208 (“Contracts will be interpreted to
‘give each provision and term effect’ and not render any terms ‘meaningless or
illusory.’” (quoting Osborn, 991 A.2d at 1159)); Kuhn Constr., Inc. v. Diamond
State Port Corp., 990 A.2d 393, 396–97 (Del. 2010) (explaining that the court “will
37 read a contract as a whole and . . . will give each provision and term effect, so as not
to render any part of the contract mere surplusage”).
Although the plain language of the Merger Agreement allows for Milestone
Payments under CPT codes “different” from 64624, Defendant’s argument that it
does not need to show actual use of a code to trigger a Milestone Payment under a
different code is incorrect. This interpretation lacks support in the plain language of
the Merger Agreement, and Defendant’s flurry of counterarguments is unavailing.
First, Defendant points to the word “effective” in the main phrase and contends that
being “effective” is the only requirement. But, as the court has already explained,
the parenthetical imposes an additional requirement for “different” CPT codes—
they must be both effective and used. Next, Defendant highlights that there is no
express language in the Merger Agreement which requires Fortis to provide
evidence of usage—but the absence of such requirement does not make the usage
condition unreasonable. In any event, here Pacira bears the burden of providing
calculations with respect to Milestone Payments it believes to have been triggered,
while Fortis is required only to submit a basis for payment if it is submitting a
milestone objection notice. 108 Defendant also halfheartedly contends that Pacira
108 Id. § 1.15(f). For example, it was Pacira that notified Fortis that two separate CMS Reimbursement Milestones had been achieved with respect to CPT code 64624 and then proceeded to pay the applicable milestones. PTO ¶¶ 85–86, 91–92.
38 prevented use by taking iovera off the market in 2020. As Plaintiffs clarify on reply,
Pacira did elect not to seek new customers for the first-generation iovera device, but
did so in response to reliability issues with the first-generation device, and, despite
not seeking new customers, continued servicing older devices.109 And, once the
second-generation device was completed, Pacira relaunched its marketing efforts at
the beginning of 2022, with two years remaining in the Milestone Achievement
Period.110 Defendant makes no attempt to show materiality,111 wrongfulness,112 or
Defendant also contends that actual use is not required because Pacira paid two CMS Reimbursement Milestones without requesting proof of physician usage. This argument fails for several reasons. First, this is extrinsic evidence. See Eagle Indus., 702 A.2d at 1232 (“If a contract is unambiguous, extrinsic evidence may not be used to interpret the intent of the parties, to vary the terms of the contract or to create an ambiguity.”). Second, it is evidence the parties agreed to exclude from interpretation of the Merger Agreement. JX 101 § 9.2 (“No prior draft of this Agreement nor any course of performance or course of dealing shall be used in the interpretation or construction of this Agreement.” (emphasis added)). Third, in any event, those two CMS Reimbursement Milestones were triggered by CPT code 64624, with respect to which, under the unambiguous language of the Merger Agreement, Pacira’s payment obligation is not conditioned on use. 109 Tr. 33:11–34:4 (Stack). 110 Id. at 34:11–17 (Stack). Stack also testified that COVID-19 and supply chain issues negatively affected Pacira’s marketing efforts and product development. Id. at 34:5–11, 34:19–23 (Stack). 111 WaveDivision Hldgs., LLC v. Millennium Digit. Media Sys., LLC, 2010 WL 3706624, at *14 (Del. Ch. Sept. 17, 2010) (“[W]here a party’s breach by nonperformance contributes materially to the non-occurrence of a condition of one of his duties, the non-occurrence is excused.” (internal quotation marks omitted)). 112 Mobile Commc’ns Corp. of Am. v. Mci Commc’ns Corp., 1985 WL 11574, at *4 (Del. Ch. Aug. 27, 1985) (“[A] party may not escape contractual liability by reliance upon the failure of a condition precedent where the party wrongfully prevented performance of that condition precedent.”); Restatement (Second) of Contracts § 245 (“There is no breach if . . . the lack of cooperation is justifiable.”).
39 the necessary state of mind 113 in response to this evidence. In fact, Defendant
abandoned this argument on reply. Instead, Defendant asserted only that Stack’s
testimony that actual usage was not required “ends the analysis and resolves the
issue.” 114 It does not. “The true test is not what the parties to the contract intended
it to mean, but what a reasonable person in the position of the parties would have
thought it meant.” Lorillard Tobacco Co. v. Am. Legacy Found., 903 A.2d 728, 739
(Del. 2006); accord Braga Inv. & Advisory LLC v. Yenni Income Opportunities Fund
I, L.P., 2020 WL 3042236, at *10 (Del. Ch. June 8, 2020) (“The legal effect of the
[Merger] Agreement, however, is an issue for the court to decide irrespective of
whatever subjective belief [Defendant or Plaintiffs] may have had about its
meaning.”); see also Paul v. Deloitte & Touche, LLP, 974 A.2d 140, 145 (Del. 2009)
(“Questions concerning the interpretation of contracts are questions of law . . . .”);
Allied Cap. Corp. v. GC-Sun Hldgs., L.P., 910 A.2d 1020, 1030 (Del. Ch. 2006)
(“Under Delaware law, the proper interpretation of language in a contract is a
question of law.”); Talkdesk, Inc. v. DM Trans, LLC, 2024 WL 2799307, at *13 (Del.
113 13 Williston on Contracts § 39:10 (4th ed.) (explaining that “the weight of authority holds that in order for prevention to constitute an excuse for nonperformance of a condition or a promise, the preventing party must have deliberately taken steps to impede performance or have arbitrarily impaired the other party’s ability to perform”). 114 Def.’s Reply Br. 26.
40 Super. May 31, 2024) (“Delaware law has long considered contract interpretation a
question of law, rather than a question of fact.”).
In sum, CPT code 64xx1 triggers the Disputed Milestones if it is effective at
a given rate, but the “different” codes only trigger the Disputed Milestones if they
are both effective and describe procedures for which iovera is actually used. This
distinction makes objective sense on the face of the Merger Agreement: 64xx1 refers
to a forthcoming code that was not usable prior to its effective date, whereas a
“different” code encompasses existing codes that could have been in use at the time
of contracting. This is the only interpretation to give meaning and effect to all of the
words governing the Disputed Milestones and is supported by the plain,
unambiguous language of the provision considered as a whole. See E.I. du Pont de
Nemours & Co. v. Shell Oil Co., 498 A.2d 1108, 1113 (Del. 1985) (“In upholding
the intentions of the parties, a court must construe the agreement as a whole, giving
effect to all provisions therein.”); Holifield v. XRI Inv. Hldgs. LLC, 304 A.3d 896,
924 (Del. 2023) (“Contracts will be interpreted to give each provision and term effect
and not render any terms meaningless or illusory. When a contract is clear and
unambiguous, the court will give effect to the plain meaning of the contract’s terms
and provisions.” (internal quotation marks omitted)). Therefore, to establish its
entitlement to the Disputed Milestones, Defendant must prove actual use of iovera
for a procedure appropriately described by its proffered CPT codes.
41 2. Defendant has not shown any use of iovera in a procedure appropriately described by CPT code 64605 or 64610.
After being confined to arguing that a national rate triggered the Disputed
Milestones, Defendant is left to argue over CPT codes 64605 and 64610.115 CPT
codes 64605 and 64610 both describe “[d]estruction by neurolytic agent, trigeminal
nerve; second and third division branches at foramen ovale,” with CPT code 64610
being the appropriate code when the procedure is performed “under radiologic
monitoring.”116 These CPT codes do not cover all procedures relating to the
trigeminal nerve; for example, CPT code 64600 applies to “[d]estruction by
neurolytic agent, trigeminal nerve; supraorbital, infraorbital, mental, or inferior
alveolar branch.”117 Therefore, Defendant must prove actual use of iovera for
destruction of “trigeminal nerve, second and third division branches at foramen
ovale” to establish that Pacira is obligated to pay the Disputed Milestones.
Defendant did not carry this burden at trial. Defendant established that iovera
has been used to treat other branches of the trigeminal nerve, but not the foramen
115 Post-trial, Defendant argued that the Disputed Milestones were triggered in 2020 by CPT codes 64600, 64605, 64610, 64640, and 64681. But because the court has determined that the Disputed Milestones can only be triggered by national reimbursement rates, Defendant concedes that the national reimbursement rates for CPT codes 64600, 64640, and 64681 do not trigger the Disputed Milestones. See Def.’s Answering & Opening Br. 24–25 (arguing that these CPT codes, regardless of whether they were considered alone, stacked, or used in combination with CPT code 76942, only triggered the Disputed Milestones under their local rates). 116 JX 229 at 5. 117 Id.
42 ovale. Defendant’s fact witness on use, Trescot, testified that she has used iovera to
treat other areas of the trigeminal nerve but has never treated the foramen ovale with
iovera.118 Defendant also points to a 2018 email discussing areas that could be
treated with iovera, which states that MyoScience had “heard of some physicians”
treating the trigeminal nerve with iovera, but did not specify the foramen ovale.119
Therefore, there is no evidence in the post-trial record that iovera has ever been used
in a procedure appropriately described by CPT code 64605 or 64610.
118 Tr. 717:10–718:10, 719:21–720:4, 738:23–739:1 (Trescot). Defendant also proffered a photograph Trescot stated was “a cryo probe passing through the foramen ovale,” but Trescot conceded that it was not a picture of a procedure she performed, she could not tell from the photograph whether the cryo probe was iovera or another device, and, though she had been told the device was iovera, she had no personal knowledge of whether the device was iovera. Id. at 727:14–21, 738:17–739:20 (Trescot). Plaintiffs made timely objections to the introduction of this evidence as hearsay at trial, and the court gave Plaintiffs a continuing objection and leave to address the issue in their post-trial briefing. Id. at 727:22–728:4. Plaintiffs raised the issue in both of their post-trial briefs, correctly identifying that Trescot’s testimony regarding use of iovera on the foramen ovale was merely repeating a statement by a third party for the truth of the matter asserted. Pls.’ Opening Br. 44 n.12; Pls.’ Reply & Answering Br. 52. By contrast, while Defendant contends that Trescot “has personally used, or has personal knowledge of the use of, the Smart Tip Products in the trigeminal nerves,” Defendant offers no response to Plaintiffs’ legal argument that Trescot’s testimony about the use of iovera to treat the foramen ovale is inadmissible hearsay. Def.’s Answering & Opening Br. 56; see also Def.’s Reply Br. 24 n.22, 28–29 (advancing arguments that other testimony was hearsay but failing to rebut Plaintiffs’ argument that Trescot’s testimony was hearsay); Emerald P’rs v. Berlin, 726 A.2d 1215, 1224 (Del. 1999) (“Issues not briefed are deemed waived.”). Therefore, the court sustains the Plaintiffs’ objection to this testimony on hearsay grounds and excludes it from the post-trial record. Beyond Trescot’s excluded testimony, there is nothing indicating that the small, blurry image included in the email located at page six of JX 400 depicts the use of iovera to treat the foramen ovale. See JX 400 at 6 (an email sent from Trescot to one of Defendant’s attorneys less than a month before trial containing only the subject line “[EXTERNAL] Iovera trigeminal” and the small black and white picture). 119 JX 15 at 3, 6–7.
43 Because Defendant has not proved that either CPT code 64605 or 64610 was
appropriate to describe a procedure in which iovera has been used, neither can trigger
the Disputed Milestones.120 Defendant does not contend that any other national
reimbursement rates triggered the Disputed Milestones and, therefore, cannot
establish that Pacira is in breach of the Merger Agreement.
III. CONCLUSION
The Merger Agreement is ambiguous as to whether the parties intended for
the Disputed Milestones to be tied to a national or a locality-adjusted reimbursement
rate. Although both sides advance reasonable interpretations of “CMS
Reimbursement,” the extrinsic evidence confirms that the parties had intended to use
the national reimbursement rate.
The earnout provision unambiguously provides that the Disputed Milestones
could be triggered by an applicable reimbursement rate for a CPT code other than
64624, but reimbursement under a different CPT code requires a procedure in which
iovera has been used. Defendant did not prove that iovera was so used.
120 The parties sparred over a wide variety of additional issues throughout the pre- and post- trial briefing, including whether proof of actual reimbursement was required, the relevance of certain CPT codes exceeding the Disputed Milestones’ monetary thresholds prior to execution of the Merger Agreement, the scope of the commercial context the court can consider in interpreting the plain language of a contract, the propriety of stacking multiple CPT codes under the language of the Disputed Milestones, and whether the facility and physician fee should be stacked when calculating reimbursement rates in the ASC setting. But, even if all these questions were resolved in Defendant’s favor, the outcome would not change. The court declines to opine upon them in dicta.
44 Plaintiffs are entitled to judgment on Count I of the complaint and Pacira is
entitled to judgment on Count I of Defendant’s counterclaim. The parties shall
confer and submit a final implementing order within ten days of this opinion.
Related
Cite This Page — Counsel Stack
Pacira BioSciences, Inc. v. Fortis Advisors LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/pacira-biosciences-inc-v-fortis-advisors-llc-delch-2025.