Partner Therapeutics Submits sBLA to FDA for BIZENGRI
Partner Therapeutics submits sBLA to FDA for BIZENGRI in NRG1 fusion-positive cholangiocarcinoma, supported by eNRGy study data showing 36.8 percent response rate and durable efficacy.
Rare Bile Duct Cancer Treatment | 15/04/2026 | By News Bureau
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