Ward v. Schaefer

89 F.4th 203
CourtCourt of Appeals for the First Circuit
DecidedDecember 22, 2023
Docket22-1547
StatusPublished
Cited by9 cases

This text of 89 F.4th 203 (Ward v. Schaefer) is published on Counsel Stack Legal Research, covering Court of Appeals for the First Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Ward v. Schaefer, 89 F.4th 203 (1st Cir. 2023).

Opinion

United States Court of Appeals For the First Circuit

No. 22-1547

VIRGINIA CORA WARD, as the administratrix of the estate of EDMUND EDWARD WARD,

Plaintiff, Appellant,

v.

ALPHACORE PHARMA, LLC and BRUCE AUERBACH,

Defendants, Appellees.

APPEAL FROM THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MASSACHUSETTS

[Hon. F. Dennis Saylor, IV, U.S. District Judge]

Before

Rikelman, Selya, and Howard, Circuit Judges.

Timothy Cornell, with whom Cornell Dolan, P.C. was on brief, for appellant. John M. Allen, with whom McCarter & English LLP was on brief, for appellee AlphaCore. Mark S. Furman, with whom Emily C. Shanahan and Tarlow, Breed, Hart & Rodgers, P.C. were on brief, for appellee Auerbach.

December 22, 2023 SELYA, Circuit Judge. This appeal tests the margins of

a court's in personam jurisdiction, consistent with the

constraints of the Due Process Clause, see U.S. Const. amend. XIV,

§ 1, and the Massachusetts long-arm statute, see Mass. Gen. Laws

ch. 223A, § 3. Stripping away unsupported assertions, we uphold

the district court's determination that the appellees, AlphaCore

Pharma, LLC (ACP) and Bruce Auerbach, lacked sufficient contacts

with the forum state to permit the exercise of in personam

jurisdiction.1 Consequently, we affirm the district court's order

of dismissal.

I

We briefly rehearse the relevant facts and travel of the

case. In reviewing a dismissal of a case for lack of personal

jurisdiction based on a prima facie record, we "take the facts

from the pleadings and whatever supplemental filings (such as

affidavits) are contained in the record, giving credence to the

plaintiff's version of genuinely contested facts" and accounting

for "undisputed facts put forth by" the parties. Baskin-Robbins

Because the appellant's claims against ACP and Auerbach 1

raise a discrete set of issues, we will resolve the appellant's claims against the remaining appellee in a separate and subsequent opinion. See, e.g., Alston v. Town of Brookline, 997 F.3d 23, 29 n.1 (1st Cir. 2021); United States v. Santiago-Rivera, 744 F.3d 229, 231 n.1 (1st Cir. 2014). Relatedly, we note that this opinion, which is based upon review of a prima facie record, does not contain the factual details that will appear in the subsequent opinion (which deals with claims based on a full trial record).

- 2 - Franchising LLC v. Alpenrose Dairy, Inc., 825 F.3d 28, 34 (1st

Cir. 2016). Withal, we do not rely on any "unsupported

allegations." Plixer Int'l, Inc. v. Scrutinizer GmbH, 905 F.3d 1,

6 (1st Cir. 2018).

ACP is a limited liability company, which has its

principal place of business in Ann Arbor, Michigan. In 2013, ACP

was acquired by MedImmune, a subsidiary of AstraZeneca

Biopharmaceuticals, Inc. (AstraZeneca). As of 2012, ACP was the

sole patent licensee of a form of recombinant human

lecithin-cholesterol acyltransferase known as ACP-501.

Auerbach is a citizen and resident of Michigan. He was

a principal of ACP, as well as a corporate officer, until ACP was

acquired by MedImmune.

The decedent, Edmund Edward Ward, was a citizen and

resident of Massachusetts. Ward was born with an extremely rare

genetic deficiency that inhibited him from being able to produce

virtually any cholesterol. As a result, Ward eventually came to

suffer from stage-5 kidney failure.

In 2012, Dr. Ernst Schaefer — Ward's treating physician

in Massachusetts — introduced Ward to Auerbach and to Drs. Robert

Shamburek and Alan Remaley as a potential candidate for ACP-501.

Ward later agreed to participate as the only subject in a long-term

trial of ACP-501. ACP donated the ACP-501 needed for the trial to

the National Institutes of Health (NIH). Despite being diagnosed

- 3 - as suffering from kidney failure, Ward postponed dialysis

treatment in order to participate in the trial.

In January of 2013, Ward traveled from his home in

Massachusetts to the NIH facility in Bethesda, Maryland, to begin

treatment. During this initial visit, Ward met with Auerbach, who

allegedly told him that the process would take a long time but

urged him to undergo the full course of the treatment, explaining

that "you will get out of it what you put into it." Auerbach

allegedly boasted that ACP-501 was "most certainly the solution"

to reverse Ward's kidney failure.

Until June of 2013, Ward traveled on a weekly basis from

his home in Massachusetts to the NIH facility in Maryland to

receive injections of ACP-501 and undergo testing (including

multiple blood draws). Beginning in July and continuing through

September of 2013, he journeyed every other week.

As part of the trial, NIH created a clinical protocol

for Ward's treatment. ACP and Auerbach each had a hand in drafting

this protocol, though the record lacks clarity as to the roles

that they played. An early draft of the protocol dated November

20, 2012, provided that, during the first phase of the trial, Ward

would receive ACP-501 injections at the NIH and then, during a

second phase, would receive them in both Maryland and

Massachusetts. The parties dispute whether this iteration of the

protocol became the final operative draft or whether a different

- 4 - draft, dated December 3, 2012, superseded it. The later draft did

not provide for any injections of ACP-501 in Massachusetts.2 In

any event, the record makes manifest — and the appellant does not

contest the fact — that all of the ACP-501 injections that Ward

received were administered at the NIH facility in Maryland.

In September of 2013, Ward withdrew from the clinical

trial. His decision to end his participation came after he was

informed that his kidney function was rapidly deteriorating and

that he was in urgent need of dialysis.

We fast-forward to July of 2016. At that time, Ward

filed a complaint against ACP, Auerbach, Schaefer, Shamburek,

Remaley, MedImmune, and AstraZeneca in a Massachusetts state

court. The complaint alleged that Ward had been fraudulently

induced to participate in the clinical trial in order to set the

table for a sale of ACP to MedImmune — a sale that was "based

principally" on the results of his trial. The complaint further

alleged that "the individual defendants, acting in concert, were

ACP shareholders, owned ACP options or warrants, or otherwise

benefited materially from the sale of ACP to [MedImmune, an

AstraZeneca subsidiary] in secret."

2It is undisputed that both drafts of the protocol stipulated that, during the periods in which Ward was at his home in Massachusetts, he would be monitored by Dr. Schaefer.

- 5 - Ward's state-court action contained a gallimaufry of

claims. One count sounded in fraud, another in lack of informed

consent, and a third in unjust enrichment. Three other counts

alleged an assortment of constitutional, civil rights, and

conspiracy claims.

In short order, the case was removed to the United States

District Court for the District of Massachusetts. See 28 U.S.C.

§ 2679(d)(2).

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