Swedish Orphan Biovitrum ABFDA declined to approve NASP, requesting additional manufacturing data, delaying market entry.

The U.S. Food and Drug Administration has issued a Complete Response Letter for Sobi's Biologics License Application for NASP, a treatment for adult patients with uncontrolled gout. The FDA is seeking additional data related to chemistry, manufacturing, and controls and contract manufacturing facilities, but raised no concerns about the clinical safety or efficacy of the product. Sobi plans to request a meeting with the FDA to discuss the feedback and will work with contract manufacturing organizations to address the deficiencies. NASP is an investigational medicine combining nanoencapsulated sirolimus and pegadricase designed to reduce serum uric acid levels.
Swedish Orphan Biovitrum ABFDA declined to approve NASP, requesting additional manufacturing data, delaying market entry.