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Sandoz takes further steps to resolve legacy U.S. Generic Drug Antitrust Class Action litigation

Sandoz U.S. has entered into a settlement agreement with the class of end payer plaintiffs for $275 million.
Levy

Sandoz has announced a number of steps to resolve the US Generic Drug Antitrust Class Action Litigation.

Following the previously announced settlements with the U.S. Department of Justice in 2020 and 2021 and with the direct purchaser plaintiffs’ class in February 2024, Sandoz has now also entered into a settlement agreement with the end payer plaintiffs’ class for a total of $275 million, which is expected to be paid before Dec. 31, 2024. 

The company also has taken a provision of $265 million for the outstanding claims brought by opt-out plaintiffs and state attorneys’ general. The settlement payment and the provision will be included in the company’s 2024 financial results. This does not affect current Sandoz full-year 2024 and mid-term guidance.

Sandoz and its subsidiary Fougera Pharmaceuticals, both indirect subsidiaries of Sandoz Group AG, have entered into a settlement agreement with the class of end-payer plaintiffs in the multi-district litigation entitled In re Generic Pharmaceuticals Pricing Antitrust Litigation in the U.S. District Court for the Eastern District of Pennsylvania. This agreement, which contains no admission of wrongdoing by Sandoz U.S., resolves all of the damages claims of the end-payer class, which is comprised generally of certain consumers, insurers, health and welfare funds, employee benefit plans and other entities that paid for and reimbursed the sales of drugs. 

[Read more: A new environment for biosimilars]

Under the terms of the agreement, Sandoz U.S. will pay $275 million in exchange for a full release of all claims asserted against it in the end-payer class action by the settlement class members.

Sandoz said this settlement underscores Sandoz commitment towards integrity and sound governance, and it is an encouraging step toward resolving allegations of legacy conduct. Beyond the payment, settlement terms include:

  • A broad release of claims that covers alleged conduct between 2009 and 2019 as well as all medicines at issue in the end-purchaser class claims
  • Class members have the right to opt out of the settlement, which could result in the settlement amount being reduced by up to $45 million.

The settlement is subject to court approval, as is required for class settlements under U.S. law. If the court preliminarily approves the settlement, class members will be notified of the settlement and given an opportunity to opt out of the class, object to the settlement and file a claim to receive a settlement payment.

[Read more: Generic drug makers continue forging ahead]

The remaining claims are seeking damages for alleged anticompetitive conduct in the U.S. market. These claims are brought by certain U.S. States and Territories as well as the indirect reseller plaintiff class and individual plaintiffs in the multidistrict litigation. Sandoz U.S. continues to defend itself in those cases and has raised a number of defenses, including whether downstream purchasers were actually damaged due to the alleged conduct. Based on its current assessment of these remaining claims, Sandoz set up a provision of $265 million. As the litigation progresses, Sandoz will continue to assess the overall situation and may increase or decrease the provision as appropriate.

In addition to the U.S. generic antitrust litigation, as previously disclosed, Sandoz, Sandoz Canada and Fougera Pharmaceuticals have been named in a class action in Ontario, Canada alleging price fixing in the Canadian generic pharmaceutical market.

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