Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination regimen consists of fluzoparib (a PARP1/2 inhibitor), camrelizumab (an anti-PD-1 monoclonal antibody), and capecitabine (an oral chemotherapy prodrug). Developed primarily by Jiangsu Hengrui Pharmaceuticals, these agents are being investigated together in various clinical settings. Specifically, a Phase II trial sponsored by Chongqing University Cancer Hospital is evaluating the sequential use of fluzoparib, either alone or in combination with camrelizumab and capecitabine, following chemoradiotherapy for untreated pan-solid tumors. These include surgically resectable rectal cancer and locally advanced unresectable non-small cell lung cancer (NSCLC), esophageal squamous cell carcinoma (ESCC), and cervical cancer. Fluzoparib works by inhibiting DNA repair in HR-deficient cells, camrelizumab enhances T-cell anti-tumor activity by blocking the PD-1/PD-L1 pathway, and capecitabine acts as a cytotoxic agent by interfering with DNA synthesis.
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 fluzoparib + camrelizumab + capecitabine.