Wright v. American Home Products Corp.

768 A.2d 518, 2000 WL 973266, 2000 Del. Super. LEXIS 231
CourtSuperior Court of Delaware
DecidedApril 20, 2000
DocketCivil Action 99C-361-JOH
StatusPublished
Cited by17 cases

This text of 768 A.2d 518 (Wright v. American Home Products Corp.) is published on Counsel Stack Legal Research, covering Superior Court of Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Wright v. American Home Products Corp., 768 A.2d 518, 2000 WL 973266, 2000 Del. Super. LEXIS 231 (Del. Ct. App. 2000).

Opinion

OPINION

HERLIHY, Judge.

Plaintiffs Evelyn and Robert- Wright have sued Evelyn Wright’s doctor, Dr. David Messenger, several Ameiican pharmaceutical companies and two French pharmaceutical companies as a result of taking a prescription diet pill, Pondimin. The two French companies, Les Labora-toires Servier [LLS] and Servier Amerique [SA] [collectively French defendants] have moved to dismiss for ineffective service of process, lack of personal jurisdiction and forum non conveniens.

Plaintiffs brought LLS and SA into this lawsuit by employing the procedures of Delaware’s long arm statute. They first had their complaint served on the Delaware Secretary of State and then mailed copies of it by registered mail to these French companies in Paris. LLS and SA contend that, as foreign companies, this method of service was not in compliance with the Hague Convention. Even if properly served, they next argue Delaware cannot exercise personal jurisdiction over them either because the long arm statute does not provide it or Due Process prevents it. Finally, in the event all these barriers are overcome, they argue Delaware is not the convenient forum for plaintiffs’ cause of action against them. Several of the issues raised by the French defendants’ motion are of first impression or extension of Delaware precedent into fresh waters.

One of the biggest problems for the Court in resolving the French defendants’ motion is sorting out their relationship with each other, with other entities and with Pondimin, the diet pill Mrs. Wright consumed. The main ingredient or other name for Pondimin is fenfluramine. There is a chemically-related diet drug, dexfen-fluramine, which is sold as Redux, with which the French defendants have some involvement. But, Mrs. Wright never took Redux.

The French defendants have submitted affidavits from two French counsel. The affidavits solve as many problems as they raise. These counsel have supplied similar affidavits in diet pill litigation elsewhere. Included in that litigation is the Multi District Litigation in the District Court for the Eastern District of Pennsylvania [MDL] concerning these diet medications. 1 This Court is indebted to an opinion of the MDL court for its efforts in sorting out this tangled web. There also has been litigation concerning one or both drugs in New Jersey and New York. LLS was the only entity, however, sued in those eases. SA was not a party in any of them in terms of opinions provided to this Court.

LLS filed similar motions to dismiss in those cases, as it has filed here. Each of the courts considering them struggled, too, to sort out the jurisdictional facts and relationships of these French defendants, to *521 other French companies related to them and to the American pharmaceutical companies. Despite access to the records in some or all of those cases and other litigation, the plaintiffs here have not presented the clearest of pictures. For instance, they lump together LLS and SA and refer to them as “Defendants Sender.” 2 Whether by design or inadvertence, this casual linking is not particularly helpful to this Court’s analysis. The Court strongly suspects there is more information which would be helpful in resolving some of the issues presented, but it is not in the record yet.

With these remarks and caveats stated, an analysis of the record presented is needed. Mrs. Wright alleges she ingested, on Dr. Messinger’s prescription orders, Pondimin from March 1995 to May 1996. She makes a number of claims of negligence relating to Pondimin, including failing to use due care in designing, testing and manufacturing, failing to properly warn, failing to provide adequate training and information about it to medical providers and more. There are claims for breach of implied warranty, breach of express warranty, strict liability and fraud. Mrs. Wright claims serious physical injury, pain and suffering and loss of income among her other claims.

The French defendants have submitted affidavits of Marc C. Milward, corporate counsel for LLS. He states that in 1963, a company known as Science-Union et Cie [SUC] licensed defendant A.H. Robins Company to manufacture and sell Pondi-min in the U.S. 3 He states that each company has its own board and officers. 4 But, he says, SUC is an “affiliated company” of LLS and SA. 5 The nature of the affiliation is not explained. Nor is it explained further in the other court opinions in which LLS has sought to be dismissed.

The licensing agreement with A.H. Robins, Milward says, provided for royalties to be paid to SUC, which ended in 1988. 6 While Pondimin continued to be sold thereafter, SUC was not involved in the marketing or selling of the drug. 7 Neither LLS nor SA, he says, received money in connection with the licensing of Pondimin. 8

Milward further explains that LLS had a licensing agreement with another U.S. company for Redux. 9 That agreement was with Interneuron and was signed in 1990. 10 In that agreement, LLS granted Interneu-ron the exclusive rights to use, manufacture and sell dexfenfluramine, Redux. The exclusive area was the U.S., Puerto Rico and U.S. territories. Interneuron was able to grant sublicenses involving Redux but only with LLS’s prior written approval. The agreement also provided other LLS controls over Interneuron. LLS was also to be kept informed of FDA application and approval process. In short, the 1990 agreement kept LLS intimately involved in the process to protect LLS’ patent and of obtaining FDA approval for Redux.

Milward states that as a result of corporate acquisitions by American Home Products [AHP], Wyeth-Ayerst [Wyeth] was marketing Redux and Pondimin in the period Mrs. Wright was taking Pondimin. 11 He goes on to state that SUC’s license agreement with A.H. Robins differs from LLS’ with Interneuron for Redux. 12 Mil-ward claims that the two drugs are differ *522 ent, have different patents by different parties and each was the object of a separate New Drug Application [NDA] to the FDA. 13 But according to an Executive Vice President for Clinical Research for Wyeth there are similarities of the main chemical components of Redux and Pondimin, dex-fenfluramine and fenfluramine. 14

In opposing the French defendants’ motions, the plaintiffs have provided several documents which tend to show SA’s involvement with fenfluramine and dexfen-fluramine.

1. A July 15, 1996 letter from SA to Wyeth listing the countries around the world where the two drugs are registered and date of registration.

2.

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Bluebook (online)
768 A.2d 518, 2000 WL 973266, 2000 Del. Super. LEXIS 231, Counsel Stack Legal Research, https://law.counselstack.com/opinion/wright-v-american-home-products-corp-delsuperct-2000.