Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Certepetide + gemcitabine + nab-paclitaxel is a three-drug combination regimen investigated primarily for the first-line treatment of advanced or metastatic pancreatic ductal adenocarcinoma (PDAC). **Certepetide** (also known by code names LSTA1 or CEND-1) is a novel cyclic peptide that selectively targets tumor vasculature and stroma, enhancing the uptake and penetration of co-administered anticancer drugs into tumors. *Gemcitabine* is a nucleoside analog that inhibits DNA synthesis, functioning as a cytotoxic antimetabolite. *Nab-paclitaxel* is a nanoparticle albumin-bound formulation of paclitaxel, a microtubule stabilizer, which enhances tumor delivery by exploiting albumin-mediated transport pathways. Together, the combination aims to improve outcomes over standard gemcitabine plus nab-paclitaxel by increasing intratumoral drug concentrations, leading to enhanced antitumor effect. The combination is under investigation in phase II clinical studies for metastatic PDAC.
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 certepetide + gemcitabine + nab-paclitaxel.