Immunization With BCG Vaccine to Prevent Tuberculosis Infection

Description

The purpose of this research is to find out if a single dose of pre-travel vaccination with BCG can lessen tuberculosis (TB) infection by producing an immune response when given to adults traveling to countries with a high burden of TB. BCG will be compared with a placebo (an inactive vaccine). BCG (Japan) is used globally but is not approved for use in the United States, therefore it is considered experimental. Participants choosing to take part in this research study, will be randomly assigned (this is like a coin flip) to BCG or placebo. 2000 eligible volunteers will be enrolled.

Conditions

Tuberculosis Infection

Study Overview

Study Details

Study overview

The purpose of this research is to find out if a single dose of pre-travel vaccination with BCG can lessen tuberculosis (TB) infection by producing an immune response when given to adults traveling to countries with a high burden of TB. BCG will be compared with a placebo (an inactive vaccine). BCG (Japan) is used globally but is not approved for use in the United States, therefore it is considered experimental. Participants choosing to take part in this research study, will be randomly assigned (this is like a coin flip) to BCG or placebo. 2000 eligible volunteers will be enrolled.

A Proof-of Concept, Randomized, Controlled Study of Tuberculosis Immunization With BCG to Prevent Infection in Healthy Adults (TIPI Trial)

Immunization With BCG Vaccine to Prevent Tuberculosis Infection

Condition
Tuberculosis Infection
Intervention / Treatment

-

Contacts and Locations

New Haven

Yale University School of Medicine, New Haven, Connecticut, United States, 06510

Washington

MedStar Washington Hospital Center/MedStar Health Research Institute, Washington, District of Columbia, United States, 20010

Decatur

Hope Clinic of the Emory University Vaccine Center, Emory University, Decatur, Georgia, United States, 30030

Boston

The Brigham and Women's Hospital Center for Clinical Investigation, Boston, Massachusetts, United States, 02115

Houston

Baylor College of Medicine, Houston, Texas, United States, 77030

Salt Lake City

University of Utah School of Medicine, Salt Lake City, Utah, United States, 84108

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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 TB burden countries for a duration of \>4 weeks and \<6 months for HCW, or ≥6 months and ≤2.5 years if long term traveler and/or/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
  • 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
  • * 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

Ages Eligible for Study

18 Years to 65 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Henry M. Jackson Foundation for the Advancement of Military Medicine,

Naomi E. Aronson, MD, STUDY_CHAIR, Uniformed Services University of the Health Sciences

Merlin L. Robb, MD, STUDY_DIRECTOR, Henry M. Jackson Foundation for the Advancement of Military Medicine

Study Record Dates

2027-09-30