Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
2141-V11 is a Fc-engineered monoclonal antibody that acts as an agonist of CD40 (Tumor necrosis factor receptor superfamily member 5), a member of the tumor necrosis factor receptor superfamily expressed on antigen-presenting cells. By binding to CD40, 2141-V11 stimulates immune cell activation and promotes antitumor immune responses. The antibody has been engineered for enhanced binding to the inhibitory FcγRIIB receptor, which increases its immunostimulatory activity and antitumor efficacy compared to earlier anti-CD40 antibodies. Preclinical studies demonstrated that intratumoral administration can induce local and systemic antitumor effects with reduced toxicity compared to systemic delivery. Clinical trials have shown promising safety and preliminary efficacy in patients with metastatic cancers such as melanoma, breast carcinoma, bladder cancer, and malignant glioma. The drug was initially developed by Duke University and is currently in phase 2 clinical development[1][3][4][5][6].
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 2141-V11.