Alvotech’s hopes of obtaining US approval for an interchangeable high-concentration adalimumab biosimilar in April hinge entirely on a successful US Food and Drug Administration facility reinspection, expected by March, the company has confirmed, revealing that the FDA had now provided assurances that the AVT02 candidate could be approved as interchangeable based on data provided in the firm’s US filing.
“The US FDA has confirmed that the goal date for an approval decision on Alvotech’s license application for AVT02 is...






