Doxecitin and Doxribthymine in Adult Subjects With Thymidine Kinase 2 (TK2) Deficiency

Recruiting now · Phase 2

Conditions studied: Thymidine Kinase 2 (TK2 ) Deficiency, Mitochondrial Myopathies

In brief

The purpose of this clinical trial is to evaluate the efficacy and safety of Doxecitin and Doxribtimine (dC+dT) in adult participants with thymidine kinase 2 (TK2) deficiency attended in the Neuromuscular Unit of '12 de Octubre' Hospital. The main questions it aims to answer are: * Is dT+dC effective in the treatment of the adult participants with TK2 deficiency? * Is dT+dC safe in the treatment of adult participants with TK2 deficiency? Researchers will evaluate the effectiveness of the treatment doxecitin and doxribthymine in adult participants with TK2 deficiency. In addition, the mitochondrial DNA levels before and after treatment (extracted from the muscle and from uroepithelial cells) of these participants will be also studied.

Key facts

Study ID: NCT06754098
Run by: Cristina Domínguez González
People needed: 15
Starts: 2025-01-01
Expected to finish: 2027-12-31
Last updated by the study team: 2025-07-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Signed informed consent by the subject.
Subject must be greater than 18 years of age at time of consent.
Genetic diagnosis of TK2 deficiency
Subject should have evidence of a moderate to severe disease, with motor and or respiratory involvement, shown by one of the following:
North Star Ambulatory Assessment Scale (NSAA) less than 30
6-minute walking test less than 450 meters
Force Vital Capacity in the sitting position less than 70 percent or a drop in the decubitus position greater than 10 percent or need for mechanical ventilation.
Disabling symptoms and evidence of motor and/or respiratory function progressive decline.
Female subjects must have no intention to become pregnant during the study. Female subjects who are of childbearing potential (that is, following menarche until at least 1 year post-menopausal if not anatomically and physiologically incapable of becoming pregnant) must agree and commit to the use of highly effective methods of birth control for the duration of the study and for 30 days after the end of the study, and be willing to have additional pregnancy tests conducted during the study. Acceptable methods are defined as those that result, alone or in combination, in a low failure rate (that is, less than 1 percent per year) when used consistently and correctly, such as surgical sterilization, an intrauterine device, or hormonal contraception in combination with a barrier method.
Male subjects with partners of childbearing potential must agree to use effective contraception methods during the study and for at least 90 days after the last dose of the study medication. Acceptable methods include the use of condoms combined with spermicidal foam/gel/film/cream/suppository.
Willingness to comply with the study protocol, including but not limited to, all study procedures, study visits, and study drug compliance.

You may not qualify if…

History of liver disease, or liver function test results (alanine aminotransferase [ALT], aspartate transaminase [AST], or total bilirubin) greater than or equal2 times (2X) the upper limit of normal. Patients with transaminases greater than 2 times (2X) can participate with the approval and monitoring of a doctor specializing in liver toxicity.
Participation in a previous trial of any investigational agent for primary mitochondrial disease within 1 year prior to informed consent, or use of any other investigational therapy within 30 days (or 3 half-lives, whichever is longer) prior to informed consent, or participation in other clinical studies, within 30 days prior to informed consent, which in the opinion of the study Sponsor, may potentially confound results from this study.
Pregnant (females 10.0 years old or older will have a pregnancy test at screening), or breastfeeding

Where it is running

Hospital Universitario 12 de Octubre — Madrid, Spain (enrolling)

Full record on ClinicalTrials.gov

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