FDA Grants Fast Track Designation to BeOne Medicines' BGB-B2033 for Liver Cancer

Reuters12-18 19:00

FDA Grants <a href="https://laohu8.com/S/FTRK">Fast Track</a> Designation to BeOne Medicines' BGB-B2033 for Liver Cancer

BeOne Medicines AG has received Fast Track Designation from the U.S. Food and Drug Administration (FDA) for its investigational treatment BGB-B2033, a GPC3x4-1BB bispecific antibody, for adult patients with hepatocellular carcinoma $(HCC)$ who have experienced disease progression following prior systemic treatment. The designation is intended to expedite the development and review of therapies that address unmet medical needs in serious conditions. BeOne is currently conducting a global Phase 1 clinical trial to evaluate the safety and anti-tumor activity of BGB-B2033, both as a monotherapy and in combination with the PD-1 inhibitor TEVIMBRA® (tislelizumab).

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. BeOne Medicines AG published the original content used to generate this news brief via Business Wire (Ref. ID: 20251218127420) on December 18, 2025, and is solely responsible for the information contained therein.

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