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Mycobacterium Tuberculosis Complex Cell-free DNA (Mtb-cfDNA) for the Pharmacometric Assessment of Anti-tuberculosis Treatment: a Proof-of-concept Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Tuberculosis (TB) is a leading infectious cause of death worldwide. Current strategies for monitoring TB treatment response are culture dependent and insensitive. New methods of assessing treatment response in vivo could inform new drug development and other treatment strategies. Cell-free DNA (cfDNA) - small circulating fragments of DNA - is widely used in maternofetal medicine and oncology for diagnosis and assessment of treatment response. This study aims to investigate whether pathogen derived Mycobacterium tuberculosis-specific cfDNA (Mtb-cfDNA) can be used to monitor TB treatment response. This feasibility study will take place at Mae RaMat TB Center in Thailand and includes two study groups: 1. Assay Development and Validation 2. Longitudinal Assessment of Mtb-cfDNA levels

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ Participants with a new diagnosis of tuberculosis

• Aged ≥ 18 years old

• Newly microbiologically confirmed (culture or nucleic acid amplification test) diagnosis of Mycobacterium tuberculosis (Mtb.) infection (of any site)

• Has not yet commenced antituberculosis therapy

• Able to understand study procedures and requirements and is able to give informed consent

⁃ For healthy volunteers:

• Aged ≥ 18 years old

• Healthy as judged by a responsible physician

• Able to understand study procedures and requirements and is able to give informed consent

Locations
Other Locations
Thailand
Shoklo Malaria Research Unit (SMRU)
RECRUITING
Tak
Contact Information
Primary
Htet Ko Ko Aung, Dr
htetkoko@shoklo-unit.com
055 581 135
Backup
François Nosten, Professor
francois@tropmedres.ac
055 532026
Time Frame
Start Date: 2025-07-21
Estimated Completion Date: 2027-09-30
Participants
Target number of participants: 140
Treatments
Group 1: Assay development and validation
Twenty participants with a new diagnosis of tuberculosis will have venous blood collected prior to treatment initiation. Twenty participants without clinical evidence of tuberculosis infection will be recruited from the local community as a control during assay validation. This group of the study participants will be assessed at day zero only.
Group 2: Longitudinal Assessment
In this group, tuberculosis participants (n= 120) will have longitudinal sampling performed from diagnosis to the end of treatment. This will establish the feasibility of dynamic Mtb-cfDNA measurements for the assessment of tuberculosis treatment response.
Related Therapeutic Areas
Sponsors
Leads: University of Oxford

This content was sourced from clinicaltrials.gov