FDA again rejects Hengrui and Elevar’s liver cancer combo

24 March 2025

The US regulator has once again declined to approve Hengrui Pharmaceuticals' (SHA: 600276) PD-1 inhibitor camrelizumab, further delaying the drug's entry into the American market.

The Chinese pharmaceutical company and its US partner, Elevar Therapeutics - a subsidiary of South Korea's HLB (Kosdaq: 028300) - received a second complete response letter from the Food and Drug Administration, citing unresolved manufacturing issues related to camrelizumab, according to a filing by Hengrui to the Shanghai Stock Exchange.

The proposed treatment combines camrelizumab with the VEGFR inhibitor Tulvegio (rivoceranib) for the first-line treatment of patients with unresectable or metastatic liver cancer.

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