Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Deoxycytidine is a naturally occurring pyrimidine nucleoside being investigated by Virginia Commonwealth University as a chemoprotectant for use in combination with high-dose cytarabine (Ara-C) therapy. It serves as a substrate for deoxycytidine kinase (dCK), the enzyme responsible for the initial phosphorylation and activation of cytarabine. By competing with cytarabine for dCK, deoxycytidine is intended to modulate the metabolism and reduce the systemic toxicity of high-dose cytarabine, potentially protecting normal tissues while maintaining the drug's anti-leukemic efficacy. It has been evaluated in Phase I clinical trials for the treatment of various hematologic malignancies, including acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML), lymphoma, and multiple myeloma.
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 deoxycytidine.