Tuberculosis
Conditions
Brief summary
This phase IV clinical study trial will be conducted among persons who require treatment for LTBI treatment in Iqaluit, Nunavut and Ottawa, Ontario. The primary objective of this study is to compare the proportion of people who complete directly observed prophylactic treatment (DOPT) using the new 3HP regimen to the current standard of 9 months INH.
Detailed description
The treatment of latent tuberculosis infection (LTBI) is a vital component of the overall strategy to reduce TB in a population. Treatment prevents ongoing transmission in communities by preventing the development of active TB disease. The current international standard for the treatment of LTBI is 9 months of Isoniazid (INH). Adherence to this lengthy regimen is one of the greatest impediments to treatment. A recent multi-centered, multi-national randomized control non inferiority trial with approximately 4,000 patients per arm demonstrated that Rifapentine and INH (3HP) given once weekly for a total of 12 doses was as effective as 9 months (252 doses) of daily INH treatment for LTBI.(1) These findings were also replicated in the pediatric population through a pediatric cohort (n=905 eligible participants) nested within the multi-centered international randomized controlled trial with children between ages 2-17 treated with 3HP compared to the INH standard for LTBI.(2) The efficacy and safety of this new regimen have been established. Rifapentine was approved by the United States Food and Drug Administration (FDA) in December of 2014 for the treatment of LTBI but is not yet approved in Canada. The shortened treatment course could increase the number of people who complete LTBI treatment which could lead to a decrease in active TB cases.
Interventions
DRUG3HP
An interrupted time series study design will be used to determine if the introduction of the 3HP regimen will result in more people completing LTBI treatment compared to the standard of 9 months INH twice weekly.
Sponsors
Government of Nunavut
Government of Canada
Ottawa Hospital Research Institute
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
2 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Males or non-pregnant, non-nursing females between the ages of 2-65 years 2. LTBI diagnosis as per Canadian TB Standards using either the Tuberculin Skin Test (TST) or the Interferon Gamma Release Assay (IGRA) 3. Children 2-5 years with negative TSTs who have been in close contact with a case of active TB disease recently 4. Able and willing to provide fully informed consent or parent/guardian able to provide consent
Exclusion criteria
1. Suspected or confirmed active TB disease 2. Known allergies to any of the study medications by participant self-report 3. Female participants of childbearing potential who: 1. have a positive pregnancy test at screening, or 2. are not willing to use a reliable method of barrier contraception during the study, or 3. are breastfeeding 4. Unable/unwilling to substitute medications with drug interactions with 3HP, including : 1. hormonal contraception 2. HIV infected participants who are on anti-retroviral drugs 3. other drugs that interact with 3HP (see Table 1) 5. Known contact with an INH or rifampin resistant case 6. Weight \< 10 kg 7. Evidence of possible liver damage defined by an aspartate transaminase (AST) level that is more than 3x the upper limit of normal in an asymptomatic patient 8. Porphyria reported by patient 9. Inability to adhere to protocol. 10. Patients may be excluded from the study for other reasons, at the investigator's discretion with detailed documentation.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Completion of treatment | 3 months | Participants who start and complete treatment |
Countries
Canada
Outcome results
None listed