Shareholder Representative Services, LLC v. Alexion Pharmaceuticals, Inc.

CourtCourt of Chancery of Delaware
DecidedSeptember 1, 2021
DocketC.A. No. 2020-1069-MTZ
StatusPublished

This text of Shareholder Representative Services, LLC v. Alexion Pharmaceuticals, Inc. (Shareholder Representative Services, LLC v. Alexion Pharmaceuticals, Inc.) 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.

Bluebook
Shareholder Representative Services, LLC v. Alexion Pharmaceuticals, Inc., (Del. Ct. App. 2021).

Opinion

IN THE COURT OF CHANCERY OF THE STATE OF DELAWARE

SHAREHOLDER REPRESENTATIVE ) SERVICES LLC, solely in its capacity as ) representative of the Securityholders, ) ) Plaintiff/Counterclaim-Defendant, ) ) v. ) C.A. No. 2020-1069-MTZ ) ALEXION PHARMACEUTICALS, INC., ) ) Defendant/Counterclaim-Plaintiff. ) ORDER DENYING DEFENDANT’S MOTION TO DISMISS

WHEREAS, on review of Defendant’s motion to dismiss (the “Motion”), as

briefed and taken under advisement on June 2, 2021, it appears:1

A. Defendant Alexion Pharmaceuticals, Inc. (“Alexion”) is an

international pharmaceutical company focused on developing and commercializing

drugs to treat rare diseases. On November 2, 2018, Alexion closed its acquisition of

Syntimmune, Inc., a biopharmaceutical development company in the same space

(the “Merger”). Before the Merger, Syntimmune had patented and was developing

a pharmaceutical candidate, known as “SYNT001,” to treat rare autoimmune

diseases.2 In the period leading up to the Merger, Syntimmune completed several

1 For the purposes of the pending Motion, I draw the relevant facts from the Verified Complaint. See Docket Item (“D.I.”) 1 [hereinafter “Compl.”]. 2 Alexion subsequently renamed SYNT001 “ALXN1830.” For clarity’s sake, I refer to SYNT001 by its original name, which the plaintiff used in its complaint. long-term animal toxicology and pharmacology studies on SYNT001, which

showed promise for eventual human testing and regulatory approval.

B. The parties memorialized the Merger in the “Merger Agreement”

between Alexion, Syntimmune, and Plaintiff Shareholder Representative Services,

LLC (“SRS”), which represented Syntimmune’s pre-Merger stockholders and

option holders (the “Securityholders”). 3 Through the Merger, Alexion acquired

SYNT001, as well as any finished and in-process drug product derived from it.

C. In return, Syntimmune’s Securityholders received $400 million in cash,

with the possibility of an additional $800 million in earn-out payments based on

SYNT001’s development (the “Earn-Out Payments”). These payments are triggered

by eight “Milestone Events,” described in Section 3.8(a) of the Merger Agreement:

(i) a one-time payment of One Hundred Thirty Million Dollars ($130,000,000) upon the earlier of (A) the successful completion of a Phase I Clinical Trial of the SC Formulation as demonstrated by achievement of the criteria set forth on Exhibit I or (B) submission to the FDA of a protocol for a Pivotal Clinical Trial for any subcutaneous formulation;

(ii) a one-time payment of One Hundred Twenty Million Dollars ($120,000,000) upon the first dosing of the first patient in a Pivotal Clinical Trial for any first Indication;

(iii) a one-time payment of One Hundred Twenty Million Dollars ($120,000,000) upon the first dosing of the first patient in a Pivotal Clinical Trial for a second Indication.

3 Compl. Ex. 1 [hereinafter “Merger Agr.”].

2 (iv) a one-time payment of One Hundred Fifty Million Dollars ($150,000,000) upon receipt of Regulatory Approval from the FDA for any first Indication;

(v) a one-time payment of One Hundred Fifty Million Dollars ($150,000,000) upon receipt of Regulatory Approval from the FDA for a second Indication;

(vi) a one-time payment of Twenty-Five Million Dollars ($25,000,000) upon receipt of Regulatory Approval from the EMA for any first Indication;

(vii) a one-time payment of Twenty-Five Million Dollars ($25,000,000) upon receipt of Regulatory Approval from the EMA for a second Indication; and

(viii) a one-time payment of Eighty Million Dollars ($80,000,000) (the “Sales Earn-Out Payment”) upon the determination at the end of Buyer’s fiscal year that the Net Sales for such fiscal year across all Indications equals or exceeds One Billion Dollars ($1,000,000,000) (the “Sales Earn-Out Goal”).4

Alexion must pay these amounts no matter when it achieves the Milestone Events. 5

4 Id. §§ 3.8(a)(i)–(viii). If Alexion achieves the Milestone Events out of order, Section 3.8(d) provides that earlier milestone payments would automatically become due once later milestones were reached: If any given Earn-Out Payment is due and one or more previous Earn-Out Payments would reasonably have been anticipated to precede such Earn-Out Payment for the achievement of Milestone Events have not been paid for any reason, then payment of all such preceding unpaid Earn-Out Payments will be due at such time as well. For example, if Earn-Out Payment (ii) were to become due, and Milestone Event (i) has not yet been achieved and accordingly Earn-Out Payment (i) had not been paid, then Earn-Out Payment (i) will become due at the time Earn-Out Payment (ii) becomes due. Id. § 3.8(d). 5 Id. §§ 3.8(k)–(l).

3 D. In addition to committing to paying SRS for certain results, Alexion

also committed to a standard of diligence in pursuit of those results for the first seven

years after closing. Section 3.8(f) provides:

For a period of seven (7) years following the Closing Date, [Alexion] shall and shall cause its Affiliates (including the Company) to use Commercially Reasonable Efforts to achieve (or cause its Affiliates, licensees or sublicensees with respect to rights to develop or commercialize the Product to achieve) each of the Milestone Events . . .6

The Merger Agreement defines “Commercially Reasonable Efforts:”

“Commercially Reasonable Efforts” means, with respect to the Product, using such efforts and resources typically used by biopharmaceutical companies similar in size and scope to [Alexion] for the development and commercialization of similar products at similar development stages taking into account, as applicable, the Product’s advantages and disadvantages, efficacy, safety, regulatory authority-approved labeling and pricing, the competitiveness in the marketplace, the status as an orphan product, the patent coverage and proprietary position of the Product, the likelihood of development success or Regulatory Approval, the regulatory structure involved, the anticipated profitability of the Product, and other relevant scientific, technical and commercial factors typically considered by biopharmaceutical companies similar in size and scope to [Alexion] in connection with such similar products. The obligation to use such efforts and resources, however, does not require that [Alexion] or its Affiliates act in a manner which would otherwise be contrary to prudent business judgment and, furthermore, the fact that the objective is not actually accomplished is not dispositive evidence that [Alexion] or any of its Affiliates did not in fact utilize its Commercially Reasonable Efforts in attempting to accomplish the objective.7

6 Id. § 3.8(f). 7 Id. § 1.1 (defining “Commercially Reasonable Efforts”). It appears the “Product” is SYNT001. See id. (defining “Product”); see also id. Ex. H.

4 E. Section 3.8(h) requires Alexion to provide SRS with written annual

reports detailing SYNT001’s development and Alexion’s efforts to achieve the

Milestone Events (each an “Annual Report”).8 Section 8.1 of the Merger Agreement

also provides that the Securityholders would indemnify Alexion for losses caused

by various breaches of various obligations, including Syntimmune’s representations

and warranties.9 Ten percent of the upfront purchase price ($40 million) was placed

in escrow to cover potential indemnification claims, to be released to the

Securityholders eighteen months after closing.10

F. After the Merger, Alexion initially reported successful and promising

advances in SYNT001’s development as of March 2019. The 2019 Annual Report

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Shareholder Representative Services, LLC v. Alexion Pharmaceuticals, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/shareholder-representative-services-llc-v-alexion-pharmaceuticals-inc-delch-2021.