Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GP + camrelizumab is a combination therapy consisting of the chemotherapy regimen "GP" (gemcitabine plus cisplatin) and the immune checkpoint inhibitor camrelizumab. Camrelizumab is a humanized monoclonal antibody that targets the programmed cell death protein 1 (PD-1) receptor on T cells, B cells, and natural killer cells. By blocking PD-1, camrelizumab prevents its interaction with PD-L1 on tumor cells, thereby enhancing anti-tumor immune responses[3][4][5]. The GP regimen (gemcitabine and cisplatin) is a standard cytotoxic chemotherapy used in various solid tumors. This combination aims to leverage both direct cytotoxic effects from chemotherapy and immune-mediated anti-tumor activity from checkpoint inhibition. Camrelizumab has been developed primarily by Jiangsu Hengrui Medicine for multiple cancer indications including hepatocellular carcinoma, Hodgkin lymphoma, esophageal squamous cell carcinoma, nasopharyngeal carcinoma, and non-small cell lung cancer[1][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 GP + camrelizumab.