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Camurus announces FDA acceptance of NDA resubmission for Oclaiz

Camurus (CAMRF) announced that the U.S. Food and Drug Administration has accepted for review the company’s resubmission of the New Drug Application for Oclaiz, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act target action date of 10 June 2026.

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