Ward v. Schaefer

89 F.4th 203
Court of Appeals for the First Circuit·Decided December 22, 2023·No. 22-1547·Published·Cited by 9 cases

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).

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

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

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.

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). As relevant here, ACP and Auerbach moved to dismiss their claims for want of in personam jurisdiction. See Fed. R. Civ. P. 12(b)(2). In support, Auerbach submitted two affidavits in which he attested that neither he nor ACP had any relevant contacts with the Commonwealth of Massachusetts. Nor had either of them — these affidavits declared — supplied any good or service within the state. Auerbach further attested that all of his and ACP's activities and communications concerning Ward — including ACP's involvement in helping the NIH prepare an investigational new drug application, ACP's donation of ACP-501 to the NIH, his two meetings with Ward at the NIH in January of 2013, and a brief telephone call with Ward in September of 2014 — occurred outside of Massachusetts. Ward neither submitted any counter-affidavits nor otherwise refuted Auerbach's representations.

The district court granted ACP's and Auerbach's joint motion to dismiss over Ward's objection. See Ward v. Auerbach, No. 16-12543, 2017 WL 2724938, at *13 (D. Mass. June 23, 2017).

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

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