Nucleoside Therapy in Patients With Telomere Biology Disorders

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Maximum Age: 70
Healthy Volunteers: f
View:

• Age ≥ 1 year and ≤ 70 years

• Karnofsky performance status ≥ 50 for participants ≥16 years of age and Lansky performance status ≥ 50 for participants \<16 years of age

• Diagnosis requirement. Participants must meet at least one of the following requirements for a diagnosis of a telomere biology disorder:

‣ Age-adjusted mean telomere length \< 1%ile in peripheral blood lymphocytes by flow cytometry-fluorescence in situ hybridization (flow-FISH), as reported by a Clinical Laboratory Improvement Amendments (CLIA)-approved laboratory

‣ OR

⁃ Pathogenic or likely pathogenic variant(s) in one of the follow telomere biology associated genes: DKC1, TERC, TERT, NOP10, NHP2, WRAP53/TCAB1, TINF2, CTC1, RTEL1, ACD, PARN, NAF1, STN1, ZCCHC8, POT1, RPA1, DCLRE1B, TYMS, as reported by a CLIA-approved laboratory.

• Participants must exhibit at least one active clinical manifestation associated with a telomere biology disorder, in the judgment of the PI, which includes but is not limited to the following: one or more peripheral blood cytopenias, bone marrow hypocellular for age, pulmonary abnormalities, liver abnormalities, gastrointestinal bleeding, immunodeficiency or immune dysregulation, ophthalmologic abnormalities, or neurologic abnormalities.

• Participants must be able to take enteral liquids by mouth or enteral feeding tube.

• Female participants who are sexually active and could become pregnant must use two effective methods of contraception, at least one of which must be considered a highly effective method.

• Participants (or parent/legally authorized representative for minors) must demonstrate the ability to understand and willingness to provide informed consent, which will be documented using an institutionally approved informed consent procedure.

Locations
United States
Massachusetts
Boston Childrens Hospital
RECRUITING
Boston
Contact Information
Primary
Helen Reed, MD, MPH
helen.reed@childrens.harvard.edu
857-218-4578
Backup
Elizabeth Korn, BS
elizabeth.korn@childrens.harvard.edu
857-218-4578
Time Frame
Start Date: 2025-09
Estimated Completion Date: 2029-06
Participants
Target number of participants: 36
Treatments
Experimental: dC/dT
Participants will take study therapy three times daily over 24 weeks with dose escalation.
Sponsors
Leads: Suneet Agarwal

This content was sourced from clinicaltrials.gov

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