Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
C-1311 is a synthetic **imidazoacridinone derivative** developed as an anti-tumor agent. It acts primarily as a DNA-damaging agent through **intercalation/alkylation**, causing DNA strand breaks by inhibiting DNA topoisomerase II, and halting cancer cell proliferation. C-1311 also acts as a **FLT3 (Fms-like tyrosine kinase 3) inhibitor** and mitosis inhibitor, with additional activities such as inhibition of receptor kinases (notably FLT3), cytochrome P450 1A2 and 3A4 isoenzymes, and angiogenesis via the HIF-1α/VEGF pathway. It was investigated in clinical trials for multiple cancers (AML, breast, colorectal, lymphoid), but development has been discontinued. The drug induces p53-dependent senescence in non-cancerous cells and mitotic catastrophe/apoptosis especially in p53-deficient cancer cells. It also has radiosensitizing properties.[1][2][3][4][5]
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 C-1311.