Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cytosine deaminase is an enzyme that catalyzes the conversion of cytosine to uracil by hydrolytic deamination. It is primarily utilized in targeted cancer gene therapy, especially in suicide gene therapy where the bacterial cytosine deaminase gene is introduced into tumor cells. When administered with the prodrug 5-fluorocytosine (5-FC), cytosine deaminase converts 5-FC into the potent anticancer agent 5-fluorouracil (5-FU), resulting in selective cytotoxicity within the tumor. Its application allows for localized chemotherapy, minimizing systemic toxicity. Cytosine deaminase can also deaminate isoguanine and isocytosine, and to a lesser extent, convert 5-FC to 5-FU, which is fundamental to the enzyme-prodrug approach used in clinical and preclinical studies for colorectal, breast, and head/neck tumors[3][6][7].
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 cytosine deaminase.