Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
HRS-4508 + capecitabine is an investigational combination therapy comprising the small molecule HRS-4508 and the cytotoxic agent capecitabine. HRS-4508 is a chemical drug developed by Jiangsu Hengrui Pharmaceuticals for the potential treatment of advanced solid tumors, including non-small cell lung cancer (NSCLC). Capecitabine is an oral prodrug of 5-fluorouracil (5-FU), routinely used in chemotherapy. Early-phase clinical trials are evaluating this combination’s safety, pharmacokinetics, and anti-tumor efficacy endpoints such as objective response rate, duration of response, progression-free survival, and overall survival in solid tumors, notably NSCLC. The exact molecular target and mechanism of HRS-4508 have not been publicly disclosed as of June 2025, but ongoing studies are monitoring blood concentrations and combination effects[4][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 HRS-4508 + capecitabine.