July 01, 2026
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The FDA has declined to approve Sobi’s investigational infusion of nanoencapsulated sirolimus plus pegadricase for adults with uncontrolled gout, according to a press release from the manufacturer.The FDA issued a complete response letter to Sobi requiring additional information regarding manufacturing control strategy of the biological component of the drug, as well as to address contract
July 01, 2026
1 min read
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The FDA has issued Sobi, also known as Swedish Orphan Biovitrum, a complete response letter for its combination gout treatment…

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