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 "Zantac")
A drug currently sold under the name Zantac 360 uses a different active ingredient and contains no ranitidine
GSK has agreed to pay up to $2.2 billion to settle most lawsuits in US state courts claiming that a discontinued version of the heartburn drug Zantac caused cancer, the company announced on Wednesday.
The agreement with 10 plaintiffs’ law firms resolves about 80,000 cases, or 93 per cent of cases pending against the British drugmaker in state courts nationwide, the company said. GSK also said it would pay $70 million to settle a related whistleblower lawsuit filed by a Connecticut laboratory.
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Jennifer Moore and R. Brent Wisner, lead attorneys for the plaintiffs, said in a joint statement that they were “thrilled” with the deal.
First approved by US regulators in 1983, Zantac became the world’s best-selling medicine in 1988 and one of the first to top $1 billion in annual sales. The drug was sold at different times by pharmaceutical companies GSK, Pfizer, Sanofi and Boehringer Ingelheim.
Lawsuits against the companies began piling up in both state and federal courts after the US Food and Drug Administration in 2020 asked manufacturers to pull Zantac off the market. The agency cited concerns that ranitidine could degrade into NDMA, a carcinogen, over time or when exposed to heat.
Pfizer has agreed to settle most of the Zantac cases against it in state court, according to its most recent financial statement, and Sanofi in April announced that it was settling about 4,000 cases.
Boehringer Ingelheim has not announced any major settlements, but is currently facing a trial over the drug in Oakland, California, state court. The company has denied wrongdoing.
“We continue to pursue claims against Boehringer Ingelheim for its wrongdoing for exposing millions of people to a known carcinogen for over a decade,” Moore and Wisner said.
A majority of the remaining state court cases are in Delaware, where a judge in June allowed plaintiffs to present crucial expert testimony that Zantac caused cancer. The drug companies had sought to keep that testimony out saying it was not based on sound scientific evidence, which would have ended the lawsuits, and are appealing the judge’s ruling to the Delaware Supreme Court.
The companies won a major victory in 2022 when a Florida federal court judge ruled that about 50,000 cases centralized there could not go forward because the plaintiffs’ expert testimony was not supported by reliable science. About 14,000 of those cases are being appealed, and are not part of Wednesday’s settlement.
A drug currently sold under the name Zantac 360 uses a different active ingredient and contains no ranitidine.
(Only the headline and picture of this report may have been reworked by the Business Standard staff; the rest of the content is auto-generated from a syndicated feed.)
First Published: Oct 10 2024 | 10:02 AM IST
