Teva is taking Alvotech’s manufacturing troubles into its own hands after deficiencies at an Icelandic facility led to another rejection for the partners’ Humira biosimilar last month.
The expanded partnership announced Monday includes “increased involvement by Teva regarding manufacturing and quality at Alvotech’s manufacturing facility,” the companies said in a press release.
The FDA turned down the companies’ interchangeable Humira biosimilar candidate AVT02 twice this year. A Teva spokesperson confirmed to Endpoints News that those rejections were behind the generics giant’s greater involvement. In June, regulators noted “certain deficiencies” at Alvotech’s Reykjavik facility in a complete response letter, according to Alvotech. The company gave a similar explanation upon the drug’s prior rejection in April.
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