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Elevar Therapeutics Announces FDA Acceptance of New Drug Application Resubmission for Rivoceranib in Combination with Camrelizumab as a First-line Systemic Treatment for Unresectable Hepatocellular Carcinoma

FDA sets PDUFA target action date of July 23, 2026FORT LEE, N.J., Jan. 30, 2026 (GLOBE NEWSWIRE) -- Elevar Therapeutics, Inc., a majority-owned subsidiary of HLB Co., Ltd. and a fully integrated biopharmaceutical company dedicated to elevating treatment experiences and outcomes for patients who have limited or inadequate therapeutic options, today announced the U.S. Food and Drug Administration (FDA) accepted the resubmission of a new drug application (NDA) for its investigational drug rivoceran

articleJiangsu Hengrui Pharmaceuticals Co., Ltd. Class AJanuary 30, 20265/company/jiangsu-hengrui-medicine-co-ltd/news/elevar-therapeutics-announces-fda-acceptance-of-new-drug-application-resubmission-for-rivoceranib-in-combination-with-camrelizumab-as-a-first-line-systemic-treatment-for-unresectable-hepatocellular-carcinoma
Elevar Therapeutics Announces FDA Acceptance of New Drug Application Resubmission for Rivoceranib in Combination with Camrelizumab as a First-line Systemic Treatment for Unresectable Hepatocellular Carcinoma

About this update from Jiangsu Hengrui Pharmaceuticals Co., Ltd. Class A

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FDAliver cancerElevar TherapeuticsuHCChepatocellular carcinomagastric cancerHengrui PharmaElevar Therapeutics, Inc.ElevarElevar Therapeutics, Inc