Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
JS105 + paclitaxel (albumin bound) is an investigational combination regimen consisting of JS105, a potent and selective oral inhibitor of the alpha isoform of phosphoinositide 3-kinase (PI3Kα), and paclitaxel (albumin bound), a nanoparticle albumin-bound (nab) formulation of the taxane paclitaxel. Developed by Junshi Biosciences, JS105 is designed to target the PI3K/Akt/mTOR signaling pathway, which is frequently dysregulated in solid tumors, particularly those harboring PIK3CA mutations. Paclitaxel (albumin bound) acts as a microtubule-stabilizing agent that inhibits cell division by preventing the depolymerization of tubulin. This combination is currently being evaluated in Phase Ib/II clinical trials (e.g., NCT06208410) for patients with advanced solid tumors, including breast cancer, to assess safety, tolerability, and preliminary anti-tumor efficacy.
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 JS105 + paclitaxel (albumin bound).