French drugmaker Sanofi on Wednesday announced that it has agreed to settle 4,000 U.S. lawsuits linking the discontinued heartburn drug Zantac to cancer. Sanofi did not disclose the financial terms of the deal, a report by news agency Reuters revealed.
Reportedly, the agreement, which still needs to be finalized, will resolve most of the lawsuits against the French pharmaceutical company in United States state courts, except Delaware where the majority of the cases are pending.
Sanofi did not admit any liability in the settlement, and said it is settling to avoid the expense and ongoing distraction of the litigation, Reuters reported.
“Sanofi has vigorously defended the Zantac litigation since the outset and will continue to do so,” the company said in a statement.
In Delaware state court, Sanofi still faces about 20,000 lawsuits. A judge in Delaware Superior Court in Wilmington is weighing the fate of about 70,000 cases filed against Sanofi and other defendants, including GSK, Pfizer, and Boehringer Ingelheim.
According to Reuters, Plaintiffs and defendants are awaiting a ruling from the judge on whether there is sufficient scientific evidence to support plaintiffs’ claims that Zantac causes cancer.
In 2022, the drugmakers had got a significant victory when another judge dismissed about 50,000 lawsuits making similar claims that had been consolidated in federal court in Florida.
That judge concluded that the opinions of the plaintiffs’ expert witnesses that Zantac can cause cancer were not supported by sound science. Plaintiffs are appealing that ruling. The drugmakers have maintained that there is no evidence Zantac exposed users to harmful levels of the carcinogenic chemical NDMA.
Jennifer Moore and Brent Wisner, who are the lead plaintiffs’ attorneys in the Delaware and California litigation, said on Wednesday that they were pleased that Sanofi had reached a settlement while litigation continues against other defendants.
“We are pushing forward aggressively against GSK and Boehringer Ingelheim and are preparing for multiple trials in California state court this year,” Moore said, as quoted by Reuters.
First approved in 1983, Zantac became the world’s best-selling medicine in 1988 and one of the first-ever drugs to top $1 billion in annual sales. Originally marketed by a forerunner of GSK, it was later sold successively to Pfizer, Boehringer and finally to Sanofi.
In 2019, some manufacturers and pharmacies halted Zantac sales after NDMA was detected in some pills. Some tests showed that Zantac’s active ingredient, ranitidine, could degrade into NDMA over time or when exposed to heat.
Soon, lawsuits began piling up from people who said they developed cancer after taking Zantac. Plaintiffs claimed that the companies knew or should have known, that ranitidine posed a cancer risk and that they failed to warn consumers.
In 2020, the U.S. Food and Drug Administration asked manufacturers to pull the drug off the market. Sanofi now sells Zantac360, a reformulated heartburn medicine whose active ingredient is famotidine.
