Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination regimen consisting of three agents: - **Carboplatin** is a platinum-based chemotherapeutic that forms DNA crosslinks, leading to apoptosis in rapidly dividing cells. - **Gemcitabine** is a nucleoside analog (antimetabolite) that inhibits DNA synthesis, resulting in cell death. - **Exisulind** (also known as Aptosyn) is an oral proapoptotic agent and sulfone derivative of sulindac. It acts primarily by inhibiting cyclic guanosine monophosphate phosphodiesterase (cGMP-PDE), leading to increased cGMP levels and activation of protein kinase G, which induces apoptosis selectively in precancerous and cancerous cells with minimal effects on normal tissue. This combination has been investigated primarily for advanced non-small cell lung cancer (NSCLC). Clinical trials have shown the regimen to be generally well tolerated, with hematologic toxicity being most common. The addition of exisulind was intended to enhance proapoptotic effects beyond standard chemotherapy[1][7][9].
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 carboplatin + exisulind + gemcitabine.