Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Quinacrine + capecitabine is an investigational combination therapy consisting of two small molecule drugs, quinacrine and capecitabine. Quinacrine is an acridine derivative historically used as an antimalarial and has demonstrated anticancer properties through multiple mechanisms, including inhibition of NF-κB signaling and p53 activation. Capecitabine is a prodrug of 5-fluorouracil (5-FU), a fluoropyrimidine antimetabolite that interferes with DNA synthesis in rapidly dividing cells. The combination has been studied in patients with treatment-refractory metastatic colorectal cancer (mCRC), where it showed tolerability at the maximum tolerated dose (capecitabine 1000 mg/m² twice daily on days 1–14; quinacrine 100 mg twice daily on days 1–21 of a 21-day cycle). Early-phase clinical data suggest potential activity in heavily pretreated mCRC patients[1][3].
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 quinacrine + capecitabine.