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Anadys gets FDA clearance to test hepatitis drug

US biopharmceutical firm Anadys Pharmaceuticals and Swiss drugmaker Novartis AG have gained FDA approval to begin the clinical testing of their investigational hepatitis C treatment, ANA975.

This gives Anadys the go-ahead to evaluate its lead compound ANA975 in the US. Under the companies joint development and commercialization collaboration created earlier this year, Novartis will pay Anadys $10 million in a milestone payment triggered by recent events.

The product, ANA975, is an oral toll-like receptor 7 (TLR7) agonist, which, along with other oral prodrugs aimed at treating infectious disease, form part of Anady’s collaboration with the Swiss pharmaceutical giant.

Under the agreement, Anadys is eligible to receive up to a total of $570 million in up-front and milestone payments from Novartis based on the successful development and commercialization of ANA975, including a $20 million up-front payment received in July.