Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ROSE12 is a novel monoclonal antibody developed by Chugai Pharmaceutical for the treatment of solid tumors. It is an FcγR affinity-enhanced anti-CTLA-4 switch antibody that selectively binds to cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) in an ATP-dependent manner. This design enhances its ability to deplete intratumoral regulatory T cells (Tregs) via increased affinity for Fcγ receptors (FcγRIIa and FcγRIIIa), resulting in potent anti-tumor efficacy while minimizing systemic immune activation. Preclinical studies have shown that ROSE12 outperforms non-fucosylated ipilimumab in terms of ADCC activity and tumor selectivity, with a favorable safety profile observed in animal models. The drug is currently undergoing phase 1 clinical trials as both monotherapy and combination therapy for patients with locally advanced or metastatic solid tumors[2][3][4][5][7].
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 ROSE12.