Penpulimab-kcqx (penpulimab-kcqx)

BL 761258

Penpulimab-kcqx (penpulimab-kcqx)

BL 761258

U.S. License Holder:

Akeso Biopharma

Date of License:

April-23-2025

Last Update:

June-15-2025

approved_indications FDA-Approved Indications

PENPULIMAB_KCQX is a programmed death receptor-1 (PD-1)-blocking antibody indicated:

In combination with either cisplatin or carboplatin and gemcitabine for the first-line treatment of adults with recurrent or metastatic non-keratinizing nasopharyngeal carcinoma (NPC);

As a single agent for the treatment of adults with metastatic non-keratinizing NPC with disease progression on or after platinum-based chemotherapy and at least one other prior line of therapy.

Methodology

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