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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Kampala, , Uganda
Kampala, , Uganda
Hanoi, , Vietnam
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