Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tasisulam + erlotinib is an experimental combination regimen investigated for the treatment of advanced solid tumors. **Tasisulam** (LY573636) is a small molecule anticancer agent that induces apoptosis through the intrinsic mitochondrial pathway and possesses antiangiogenic properties; it is characterized by high albumin binding, which necessitates specific exposure-based dosing strategies. **Erlotinib** is an orally active tyrosine kinase inhibitor that targets the epidermal growth factor receptor (EGFR). The combination was evaluated in Phase 1b multi-arm clinical trials to assess safety, tolerability, and pharmacokinetics in patients with advanced malignancies, including non-small-cell lung cancer (NSCLC). However, the clinical development of tasisulam was ultimately terminated by Eli Lilly following unfavorable results in other late-stage trials.
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 tasisulam + erlotinib.