Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**RP101 + gemcitabine** is an experimental combination therapy for cancer, most notably evaluated in advanced pancreatic cancer. **RP101** (also known as BVDU or (E)-5-(2-bromovinyl)-2'-deoxyuridine) is a small molecule nucleoside analogue that binds and modulates the activity of **heat shock protein Hsp27**, which is implicated in tumor cell resistance to chemotherapy and development of metastases. RP101 suppresses genes linked to drug resistance, assists in preventing chemoresistance, supports apoptosis, and enhances the efficacy of cytotoxic agents including gemcitabine. **Gemcitabine** is a nucleoside analog that inhibits DNA synthesis and is a standard first-line chemotherapeutic for pancreatic and other cancers. In multiple studies, the co-administration of RP101 and gemcitabine increased remission rates, prolonged median survival, and delayed disease progression without major additional safety signals. The combination has advanced through phase 2 and phase 2b clinical studies for advanced pancreatic cancer.
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 RP101 + gemcitabine.