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In a significant legal victory for pharmaceutical giants, the Delaware Supreme Court ruled in favor of GlaxoSmithKline,
, and Boehringer Ingelheim, dismissing the validity of expert testimony that linked the heartburn medication Zantac to tens of thousands of cancer cases. The court found that Superior Court judge Vivian Medinilla had erred in allowing the expert testimony to be presented, which had supported the claims of nearly 75,000 plaintiffs.The ruling effectively removes a major legal hurdle for the pharmaceutical companies involved in the ongoing litigation surrounding Zantac. The court's decision underscores the importance of rigorous scientific evidence in product liability cases and sets a precedent for future litigation involving similar claims. The dismissal of the expert testimony means that plaintiffs will need to find new evidence to support their claims, which could be a challenging task given the complexity of the scientific issues involved.
The court's decision also highlights the potential risks associated with relying on expert testimony in high-stakes litigation. The ruling demonstrates that such testimony can be subject to rigorous scrutiny and challenge, emphasizing the need for robust and verifiable evidence in legal proceedings. The case revolves around Zantac, a medication that has been produced by multiple pharmaceutical companies since its approval in the United States in 1983. However, concerns over its potential link to the human carcinogen N-nitrosodimethylamine (NDMA) led to its withdrawal from the market in 2020.
Since then, the manufacturers of Zantac have faced numerous cancer lawsuits, with plaintiffs alleging that the drug's primary active ingredient, ranitidine, can convert into a carcinogen when not stored at appropriate temperatures. The Delaware Supreme Court's ruling now sends these cases back to the trial court for further review of the expert testimony, potentially prolonging the legal battle and adding complexity to the plaintiffs' efforts to prove their claims.

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