SMART Local Unions & Councils Pension Fund v. BridgeBio Pharma, Inc.

CourtCourt of Chancery of Delaware
DecidedDecember 29, 2022
DocketC.A. No. 2021-1030-PAF
StatusPublished

This text of SMART Local Unions & Councils Pension Fund v. BridgeBio Pharma, Inc. (SMART Local Unions & Councils Pension Fund v. BridgeBio Pharma, 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
SMART Local Unions & Councils Pension Fund v. BridgeBio Pharma, Inc., (Del. Ct. App. 2022).

Opinion

IN THE COURT OF CHANCERY OF THE STATE OF DELAWARE

SMART LOCAL UNIONS AND COUNCILS ) PENSION FUND, on behalf of itself and all ) other similarly situated former stockholders of ) EIDOS THERAPEUTICS, INC., ) ) Plaintiff, ) ) v. ) C.A. No. 2021-1030-PAF ) BRIDGEBIO PHARMA, INC., NEIL ) KUMAR, ALI SATVAT, and UMA SINHA, ) ) Defendants. ) )

MEMORANDUM OPINION

Date Submitted: September 19, 2022 Date Decided: December 29, 2022

Thomas Curry, Tayler D. Bolton SAXENA WHITE P.A., Wilmington, Delaware; David Wales SAXENA WHITE P.A., White Plains, New York; Gregory V. Varallo BERNSTEIN LITOWITZ BERGER & GROSSMANN LLP, Wilmington, Delaware; Mark Lebovitch, BERNSTEIN LITOWITZ BERGER & GROSSMANN LLP, New York, New York; Jeremy Friedman OSTER & TEJTEL PLLC, Bedford Hills, New York; Attorneys for Plaintiff Smart Local Unions and Councils Pension Fund.

Cliff C. Gardner, Andrew D. Kinsey SKADDEN, ARPS, SLATE, MEAGHER & FLOM LLP, Wilmington, Delaware; Attorneys for Defendants BridgeBio Pharma, Inc., Neil Kumar, Ali Satvat, and Uma Sinha.

FIORAVANTI, Vice Chancellor A former stockholder of Eidos Therapeutics, Inc. (“Eidos” or the “Company”)

challenges a January 2021 merger in which BridgeBio Pharma, Inc. (“BridgeBio”)

acquired the remaining 37% of Eidos’s common stock that it did not already own

(the “Transaction”). In the Transaction, Eidos stockholders had the right to elect to

receive either 1.85 shares of BridgeBio common stock or $73.26 in cash for each

share of Eidos common stock.

The plaintiff has asserted claims alleging that BridgeBio breached its

fiduciary duties as Eidos’s controlling stockholder in connection with the merger.

The plaintiff further alleges that three Eidos directors who also served as officers or

directors of BridgeBio at the time of the Transaction breached their fiduciary duties

by approving the merger.

The defendants have moved to dismiss the complaint under Court of Chancery

Rule 12(b)(6) for failure to state a claim upon which relief can be granted. There is

no dispute that the merger was an interested transaction involving a controlling

stockholder, presumptively subject to review under the exacting entire fairness

standard. The only issue on this motion is whether the Transaction complied with

the framework established in Kahn v. M & F Worldwide Corp., 88 A.3d 635 (Del.

2014) (“MFW”), so as to subject the claims to business judgment review instead of

entire fairness. Plaintiff argues that the defendants have not satisfied four of the six

elements of the MFW framework. Central to plaintiff’s opposition is the Company’s rejection of multiple

proposals by global pharma giant GlaxoSmithKline plc (“GSK”) to partner with or

acquire Eidos. Plaintiff contends that the Company’s treatment of the GSK

proposals and the disclosures concerning those proposals in the proxy statement

render MFW inapplicable.

For the reasons explained below, the court concludes that the defendants have

satisfied MFW. Thus, the Transaction is subject to review under the business

judgment standard, and the complaint must be dismissed.

I. BACKGROUND

The facts are drawn from the Verified Stockholder Class Action Complaint

(the “Complaint”)1 and documents integral thereto, including documents produced

to the plaintiff in response to a books and records demand under 8 Del. C. § 220, and

documents otherwise subject to judicial notice.2

A. The Parties

Immediately prior to the closing of the Transaction, Eidos was a Delaware

corporation and its shares were publicly traded on Nasdaq Global Select Market

under the ticker symbol “EIDX.” Eidos is a development-stage biopharmaceutical

1 C.A. No. 2021-1030-PAF, Docket (“Dkt.”) 1 (“Compl.). 2 The parties submitted exhibits with their briefs. This opinion cites to the exhibits by reference to the party offering the exhibit and the corresponding exhibit number. E.g., Defs.’ Ex. 1.

2 company focused on developing a product to treat transthyretin amyloidosis, a

progressive condition that can lead to heart failure and other life-threatening

conditions.3 The Eidos drug, known as acoramidis or AG10, seeks to slow the

progression of the disease by stabilizing the proteins that cause the disease’s

symptoms.4

Defendant BridgeBio is a Delaware corporation headquartered in Palo Alto,

California.5 Its shares are publicly traded on the Nasdaq Global Select Market.

BridgeBio develops and commercializes treatments for genetic diseases and houses

each drug development program in a separate dedicated subsidiary.6 Immediately

prior to the Transaction, BridgeBio owned approximately 63.2% of the outstanding

shares of Eidos.7

Defendants Neil Kumar, Ali Satvat, and Uma Sinha were three of the six

members of the Eidos board of directors (the “Eidos Board”) at the time of the

3 Compl. ¶ 32. 4 Id. ¶¶ 33–34. 5 Id. ¶ 27. 6 Id. ¶ 35. 7 Id. ¶ 37.

3 Transaction.8 At that time, all three served simultaneously as a director, officer, or

both, of BridgeBio.9

Kumar served as CEO of Eidos and a director on the Eidos Board beginning

in April 2015 and continuing through the closing of the Transaction, while also

serving as a director and CEO of BridgeBio, which he co-founded.10 Satvat served

on the Eidos Board from June 2018 through the closing of the Transaction, during

which time he also served as a director of BridgeBio.11 Satvat is a partner at

Kohlberg Kravis Roberts & Co. LP (“KKR”), a private equity firm that owns

approximately 28% of BridgeBio’s stock.12 Sinha served as a director on the Eidos

Board from December 2019 through the closing of the Transaction.13 During that

time, she also served as the Chief Scientific Officer of Eidos and BridgeBio.14

B. Early History of Eidos

Eidos was founded in 2013. In 2017, BridgeBio invested $27 million in Eidos

in exchange for a majority equity stake.15 In 2018, AG10 continued to progress

8 Id. ¶ 4. The three other members of the Eidos Board, William Lis, Duke Rohlen, and Susan Hooper, were outside directors. Id. They are not named as defendants in this action. 9 Id. ¶¶ 28–30. 10 Id. ¶ 28. 11 Id. ¶ 29. 12 Id. ¶¶ 3–4. 13 Id. ¶ 30. 14 Id. ¶ 4. 15 Id.

4 through the initial stages of testing in order to obtain approval from the U.S. Food

and Drug Administration and began Phase II trials in early May 2018.16 One month

later, BridgeBio sold a minority stake in Eidos in an initial public offering (the

16 Id. ¶ 38 n.11. Before a new drug can be marketed for human use, the U.S. Food and Drug Administration (the “FDA”) must approve it. The road to approval is arduous and few new drugs ever make it from initial clinical stages to market. See In re Vaxart, Inc. S’holder Litig., 2022 WL 1837452, at *16 n.161 (Del. Ch. June 3, 2022). The sponsor of a drug begins by conducting laboratory and animal testing. If the results of that testing are satisfactory, the company will submit an Investigational New Drug (“IND”) Application to the FDA, seeking permission to begin human clinical trials. If the IND is approved, the drug enters into a three-phase investigatory testing process. 21 C.F.R. § 312.21. Phase I involves a “closely monitored, relatively small study (twenty to eighty volunteers) to determine the safety of the drug and, if possible, early evidence of effectiveness.” Vallabhaneni v. Endocyte, Inc., 2016 WL 51260, at *2 (S.D. Ind. Jan.

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