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Hengrui PD-L1/TGF-βRII bifunctional fusion protein SHR-1701 was approved for clinical use

 Last Update: 2021-08-07
 Source: Internet
 Author: User

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On June 30, Hengrui issued an announcement stating that the clinical trial application of SHR-1701 injection developed by its subsidiary Shengdia was approved by the State Food and Drug Administration, specifically the comparison of SHR-1701 injection combined with axitinib tablets A multicenter, randomized, controlled, open phase Ib/III clinical study of sunitinib malate capsules for the first-line treatment of advanced renal cell carcinoma, and SHR-1701 combined with chemotherapy compared with placebo combined with chemotherapy for the treatment of advanced or untreated advanced renal cell carcinoma.

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