Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Deferasirox + azacitidine is a combination of two pharmaceutical agents used primarily in the management of myelodysplastic syndromes (MDS) and related hematological disorders. Deferasirox is an orally administered, once-daily iron chelator that binds excess iron, facilitating its excretion and reducing iron overload commonly seen in patients receiving chronic blood transfusions[3][5]. Azacitidine is a pyrimidine nucleoside analogue with antineoplastic activity; it acts as a hypomethylating agent by inhibiting DNA methyltransferase, leading to DNA hypomethylation and direct cytotoxicity against abnormal hematopoietic cells through incorporation into RNA and DNA[1][4][6]. The combination may be considered for MDS patients who require both disease-modifying therapy (azacitidine) and management of transfusional iron overload (deferasirox).
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 Deferasirox + azacitidine.