Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
IBI323 + chemotherapy is a combination regimen of the bispecific antibody **IBI323** with standard cytotoxic chemotherapy agents. IBI323 is a recombinant bispecific monoclonal antibody that simultaneously targets **Programmed cell death ligand 1 (PD-L1)** and **Lymphocyte-activation gene 3 (LAG-3)**, both of which are immune checkpoint proteins exploited by cancers to escape immune surveillance. By blocking both PD-1/PD-L1 and LAG-3/MHC-II interactions, IBI323 aims to stimulate stronger anti-tumor T cell immunity compared to monotherapy or dual antibody combinations, and it possesses an additional cell bridging function that can bring tumor cells and immune T cells into closer contact. Preclinical studies show enhanced efficacy and greater activation of tumor-specific CD8+ and CD4+ T cells, with durable responses. This combination therapy is being tested for advanced malignant tumors, particularly where patients have progressed on standard therapies[1][2][4][5].
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 IBI323 + chemotherapy.