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Search / Trial NCT07018076

Candidate Clinical Correlate of Prognostic Outcome for TB Study

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Jun 4, 2025

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Tuberculosis Global Health Diagnostics

ClinConnect Summary

The Candidate Clinical Correlate of Prognostic Outcome for TB (C3PO) study is part of a larger research effort aimed at improving how we predict the risk of tuberculosis (TB) coming back after treatment. This study is looking for new ways to identify patients who might be at risk for recurring TB by testing different samples, like sputum (mucus from the lungs) and blood. Currently, the tools we use to predict the chance of TB returning are not very effective, so finding better methods could help in developing new treatments and improving patient care.

If you or someone you know is over the age of 12 and has successfully completed treatment for drug-susceptible TB with a standard six-month medication plan, you may be eligible to participate. However, if treatment was completed more than 14 days ago or if you have taken any medications that fight TB in the last 14 days for reasons unrelated to TB treatment, you cannot join the study. Participants will be asked to attend follow-up visits and will need to provide consent to be part of this important research. This trial is actively recruiting participants, and everyone, regardless of gender, is welcome to apply.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. . individuals age ≥ 12 years;
  • 2. . have completed treatment for drug-susceptible tuberculosis with the standard 6-month regimen of isoniazid, rifampin, pyrazinamide, and ethambutol (HRZE).
  • Exclusion Criteria:
  • 1. completed treatment for drug-susceptible tuberculosis \>14 days prior to screening/enrollment;
  • 2. routinely taking any medication with anti-mycobacterial activity (including fluoroquinolones) for any reason not related to tuberculosis treatment within the last 14 days;
  • 3. unwilling to provide informed consent or return for study follow-up visits.

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

Kampala, , Uganda

Kampala, , Uganda

Hanoi, , Vietnam

Patients applied

0 patients applied

Trial Officials

Adithya Cattamanchi, MD

Principal Investigator

University of California San Francisco; University of California Irvine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported