Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CPX-351 (Vyxeos) is a liposomal formulation containing a fixed 5:1 molar ratio of cytarabine and daunorubicin. Developed by Celator Pharmaceuticals (later acquired by Jazz Pharmaceuticals), it is specifically indicated for the treatment of adults and pediatric patients (1 year and older) with newly-diagnosed therapy-related acute myeloid leukemia (t-AML) or AML with myelodysplasia-related changes (AML-MRC). The liposomal delivery system maintains the synergistic ratio of the two drugs in the plasma and preferentially delivers them to the bone marrow, where they are taken up by leukemia cells. Cytarabine acts as a nucleoside metabolic inhibitor that interferes with DNA synthesis, while daunorubicin acts as an anthracycline that intercalates DNA and inhibits topoisomerase II.
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 CPX-351 (daunorubicin + cytarabine).