Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GB268 is a **tri-specific monoclonal antibody** designed to simultaneously target **PD-1 (Programmed cell death protein 1)**, **CTLA-4 (Cytotoxic T-Lymphocyte-Associated Antigen 4)**, and **VEGF (Vascular Endothelial Growth Factor)**. Developed by **Genor Biopharma**, this novel antibody is engineered to enhance antitumor immune activity while reducing toxicity compared to multiple individual or bispecific antibody therapies targeting these pathways. The drug is undergoing early clinical evaluation for the treatment of **advanced solid tumors**, with a primary focus on cancer immunotherapy by blocking immune checkpoints (PD-1 and CTLA-4) and inhibiting angiogenesis (VEGF)[1][2][3][5][9][7][10]. Preclinical studies have demonstrated that GB268 provides enhanced antitumor efficacy and an improved safety profile relative to combinations of monoclonal antibodies targeting the same pathways. The molecule is currently in Phase 1 clinical studies to assess its safety, tolerability, pharmacokinetics, and preliminary efficacy in patients with advanced solid tumors[3][5][7][10].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on GB268.