科州医药KECHOW PHARMA
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KeChow Pharma Announces NMPA Approval of Tunlametinib (HL-085) as the First Targeted Therapy for Patients with NRAS Mutated Advanced Melanoma and Previously Treated with PD-1/PD-L1 2024-03-18 18:02
Roche and KeChow Reach a Cooperation Agreement 2021-08-20 23:00
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