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Bolt Biotherapeutics Presents Updated Clinical Data From Phase 1 Dose-Escalation Trial Of BDC-1001 As Monotherapy And In Combination With Nivolumab In HER2-Expressing Tumors At ESMO 2023 Congress

Updated safety data supports the selection of 20 mg/kg q2w as the recommended Phase 2 dose (RP2D) Improved efficacy with one partial response (PR) improving to a complete response (CR), two additional patients with

BOLT

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CEL-SCI Corporation Announces 5-Year Head & Neck Cancer Survival Increased From 45% To 73% In Co’s Target Population, Cutting Risk Of Death In Half, As Presented At Leading Cancer Conference ESMO 2023

Target patient population for regulatory submissions finalized: Patients with low PD-L1, in contrast tocurrent checkpoint inhibitors which work best with high PD-L1. Addressing unmet need in ~145,000 head and

CVM

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Ambrx Announces ARX517, A PSMA-Targeted ADC, Demonstrates 52% PSA50 (≥50% Reduction) And A Highly Differentiated Safety And PK Profile In Patients With mCRPC, Who Progressed On Multiple FDA-Approved Treatments

Newly published data from the Phase 1 portion of the on-going Phase 1 / 2 APEX-01 trial provide the following key points: Multiple efficacy endpoints demonstrate consistent and promising anti-cancer activity at

AMAM

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Pliant Therapeutics INTEGRIS-PSC Phase 2a Interim Data Evaluating Bexotegrast In Primary Sclerosing Cholangitis To Be Highlighted In An Oral Late-Breaking Presentation At The Liver Meeting 2023

Pliant Therapeutics, Inc. (NASDAQ:PLRX), a clinical-stage biotechnology company and leader in the discovery and development of novel therapeutics for the treatment of fibrotic diseases, today announced a late-breaking

PLRX