Akeso Announces FDA Approval for Penpulimab-kcqx in Two BLA Indications for Comprehensive Treatment of Advanced Nasopharyngeal Carcinoma
- The U.S. FDA approved penpulimab-kcqx for nasopharyngeal carcinoma as announced April 24, 2025.
- This approval followed prior FDA designations highlighting critical unmet patient need.
- This differentiated antibody treats adult recurrent or metastatic non-keratinizing NPC in two settings.
- The Phase 3 AK105-304 study showed 9.6 months median progression-free survival in the treatment group.
- The approval offers a new immunotherapy option and represents Akeso's first US milestone.
35 Articles
35 Articles

Akeso Announces FDA Approval for Penpulimab-kcqx in Two BLA Indications for Comprehensive Treatment of Advanced Nasopharyngeal Carcinoma
HONG KONG, April 24, 2025 /PRNewswire/ -- Akeso, Inc. (9926.HK) ("Akeso" or the "Company") is excited to announce that the U.S. Food and Drug Administration (FDA) has approved its differentiated PD-1 monoclonal antibody, penpulimab-kcqx, in combination with cisplatin or carboplatin…
New PD-1 Inhibitor Approved for Nasopharyngeal Carcinoma
(MedPage Today) -- The FDA approved the PD-1 inhibitor penpulimab, with two indications, for treating non-keratinizing nasopharyngeal carcinoma (NPC) in adults. No trade name was indicated for the drug. The first indication -- for the first...
FDA Approves Akeso’s Penpulimab for Dual Use in Nasopharyngeal Cancer Treatment
HONG KONG, April 25, 2025 /PRNewswire/ -- Akeso, Inc. (9926.HK) ("Akeso" or the "Company") is excited to announce that the U.S. Food and Drug Administration (FDA) has approved its differentiated PD-1 monoclonal antibody, penpulimab-kcqx, in combination with cisplatin or carboplatin and gemcitabine for the first-line treatment of adult recurrent or metastatic non-keratinizing nasopharyngeal carcinoma (NPC). FDA also approved penpulimab-kcqx as a …
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