TB prevention study halted early – only 16 volunteers enrolled
NCT ID NCT04453293
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if a single dose of the BCG vaccine could prevent tuberculosis infection in healthy adults traveling to countries with high TB rates. Participants were randomly assigned to receive either BCG or a placebo. The study was terminated early and enrolled only 16 out of a planned 2000 volunteers, so no reliable conclusions can be drawn.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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16 people
The number who actually took part.
- Started
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Dec 2021
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participants will be eligible for study participation if they meet all of the following criteria: 1. Participant is willing to participate in the study as evidenced by providing voluntary written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization prior to conducting any trial related procedures 2. Participant is male or female, age ≥ 18 years and ≤ 65 years at time of consent 3. Participant is in good general health, confirmed by medical history, laboratory screening, and physical examination 4. Participant has no known history of Mtb infection 5. Participant has no prior history of BCG vaccination, or previous receipt of an investigational Mtb vaccine 6. Participant is assessed to be at risk for TB exposure (particularly drug resistant TB) during planned travel and has planned to work in high or moderate TB burden countries for a duration of a minimum of 10 days and not greater than 6 months for HCW 7. Participant presents at least 4 weeks prior to travel departure 8. Participant is willing to forego any periodic tuberculin skin test screening procedures for 6 months after receiving BCG/placebo vaccine 9. Participant is willing to wait after receiving a COVID-19 vaccine for 7 days before receiving BCG/placebo vaccine 10. Participant is willing to complete all study visits as required by the protocol and is reachable by telephone or email during the study 11. Participant agrees to medical record access for purposes of relevant medical history collection For Females of Childbearing Potential Only: 12. Participant has a negative urine pregnancy test prior to starting study treatment 13. Participant is willing to use effective contraception for at least 30 days before and 6 weeks after BCG/placebo vaccination 14. Lactating female that is willing to refrain from breast-feeding for 6 weeks post-vaccination Exclusion Criteria: * Participants will be ineligible for study participation if they meet any of the following criteria: 1. Participant has known positive tuberculin skin test (\>10 mm) or positive IGRA 2. Participant has medical condition for which BCG vaccination is contraindicated (e.g., HIV or other immunocompromised conditions) 3. Participant is currently receiving (within last 30 days) immune-compromising treatments, such as TNF-α blockade 4. Participant has history of chronic (≥ 30 days) oral steroid use or intravenous (IV) steroids within the last 90 days 5. Participant has received radiation therapy or chemotherapy within the last 180 days 6. Participant has received BCG treatment for bladder cancer 7. Participant is female and is pregnant (as defined by positive urine βHCG test) or intends to become pregnant in next 3 months, or is breast-feeding at screening or vaccination visit 8. Participant is unwilling to complete all required study elements (e.g., HIV testing) 9. Participant has received 2 or more live vaccinations (e.g., measles and yellow fever) within 30 days prior to receipt of BCG/placebo vaccine (Visit 2) 10. Participant has known or suspected hypersensitivity to BCG vaccine or related products 11. Participant has positive/borderline IGRA test at screening 12. Participant has positive/indeterminate HIV test at screening unless has received prior HIV vaccine 13. Participant has a history of life-threatening adverse event following receipt of any immunization 14. Participant is known to have a behavioral, cognitive, or psychiatric disease that in the opinion of the investigator affects the ability of the participant to understand or cooperate with the requirements of the study protocol 15. Participant has other concurrent condition(s) that in the opinion of the investigator would jeopardize the safety or rights of a participant participating in the trial or would render the participant unable to comply with the protocol and/or compromise study objectives 16. Participant has had tuberculin skin testing performed within 1 month prior to Visit 1 17. Participant has received a COVID-19 vaccine within 7 days prior to BCG/placebo vaccine 18. Participant has had a probable exposure to TB (defined as to someone with suspected or confirmed pulmonary TB who is likely infectious) within 8-10 weeks of Visit 1 19. Participant has prior history of nontuberculous mycobacterial disease, not colonization only
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Baylor College of Medicine
Houston, Texas, 77030, United States
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Hope Clinic of the Emory University Vaccine Center, Emory University
Decatur, Georgia, 30030, United States
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Johns Hopkins Bloomberg School of Public Health, Department of International Health, Center for Immunization Research
Baltimore, Maryland, 21205, United States
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MedStar Washington Hospital Center/MedStar Health Research Institute
Washington D.C., District of Columbia, 20010, United States
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The Brigham and Women's Hospital Center for Clinical Investigation
Boston, Massachusetts, 02115, United States
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University of Utah School of Medicine
Salt Lake City, Utah, 84108, United States
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Yale University School of Medicine
New Haven, Connecticut, 06510, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can new tests predict who will develop active TB?
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- TB drug liver risk under the microscope
- Health workers on doorsteps: a new push to stop TB in kids