
FDA clears IND application for novel anti-fibrotic drug AK3280 by ArkBio, leading to Phase 2 clinical trial for IPF.
On February 11, 2026, Shanghai Ark Biopharmaceutical Co., Ltd. revealed that the U.S. Food and Drug Administration (FDA) has approved its Investigational New Drug (IND) application for AK3280. This drug is a new anti-fibrotic treatment aimed at treating idiopathic conditions. This development signifies a significant step forward in the company's efforts to introduce innovative therapies into the market.

