PF-AtlasClinical Trials › NCT06817590

Nucleoside Therapy in Patients With Telomere Biology Disorders

deoxycytidine · Phase 1

Registry ID
NCT06817590
Phase
Phase 1
Status
Recruiting
Drug / intervention
deoxycytidine
Sponsor
Suneet Agarwal
Start
2025-09-29
Enrollment
36
Locations
1

About this trial

The goal of this clinical trial is to learn if a combination therapy of deoxycytidine (dC) plus deoxythymidine (dT) is safe in patients with telomere biology disorders. The main questions it aims to answer are: * Is the therapy safe with tolerable side effects in patients with telomere biology disorders? * Are problems with the bone marrow or blood or lungs changed after 6 months of dC+dT treatment in patients with telomere biology disorders? Participants will: * Take study drug by mouth three times daily for 24 weeks * Make approximately 2 visits to Boston Children's Hospital during the 24 weeks: once at the beginning of treatment and once at the end of treatment. * Go to a lab for a blood draw an additional 6 times during treatment. * Have 9 phone calls with a research nurse, including one 4 weeks after treatment ends. * Keep a diary to track doses of study drug that were taken or missed.

View NCT06817590 on ClinicalTrials.gov →

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Medical disclaimer. This page summarizes public trial data for NCT06817590 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.