Human Immunodeficiency Virus, Tuberculosis
Conditions
Keywords
TB/HIV, Phase III, Randomised
Brief summary
Tuberculosis (TB) remains a major global public health problem, particularly in low- and middle-income countries (LMICs) in Africa, Asia, and Eastern Europe. Approximately 10 million people fall sick with TB, causing up to 2 million deaths, worldwide per year. Considerable progress was made in TB control from 1990-2015, motivating the World Health Organization (WHO) to launch an ambitious EndTB strategy. However, the effect of the ongoing Coronavirus Disease 2019 (Covid-19) pandemic has been devastating and the last two years have seen the first year-on-year increases (of 5.6%) in TB mortality since 2005 . In order to regain lost ground, and re-establish progress towards elimination of TB, innovation is needed in all aspects of TB control, including development of shorter treatment regimens for drug susceptible (DS) and multi-drug resistant / rifampicin resistant (MDR/RR) forms of the disease. This protocol seeks to conduct the TB clinical trial combining the 8-methoxyfluroquinolone and optimised dose of rifamycing to address two questions. The first is to confirm the non-inferiority of a four-month optimised dose rifamycin and moxifloxacin-based regimen amongst African TB patient populations with high rates of co-incident HIV. Secondly, we seek to establish that the rifamycin of choice in potent 4-month anti-TB treatments could be rifampicin as this will be more rapidly up-scalable for public health impact.
Detailed description
The study objectives of this clinical trial are Primary effectiveness objective: To evaluate whether one or both of two experimental regimens based on optimised dose rifampicin with or without moxifloxacin and given for 16 weeks are non-inferior to standard treatment for drug-susceptible tuberculosis given for 26 weeks, as assessed by patient survival, free of tuberculosis 12 months after initiation of therapy. Primary safety objective: To evaluate whether one or both of two experimental regimens based on optimised dose rifampicin with or without moxifloxacin and given for 16 weeks are as safe and tolerable as standard treatment for drug-susceptible tuberculosis given for 26 weeks, as assessed by the frequency of Adverse Events (AEs) of Common Terminology Criteria for Adverse Events (CTCAE) grade 3 severity or higher. Participants will be individuals with bacteriological confirmed pulmonary TB aged 18 years or above, with or without HIV co-infection in Gabon, Malawi, Mozambique and Tanzania. The trial sites are also established members of the PanACEA / SimpliciTB group including the Centre de Recherches Médicales de Lambaréné (CERMEL)-Gabon, the Helse Nord Tuberculosis Initiative (HNTI) at Kamuzu University of Health Sciences (KUHES)-Malawi and the Polana Caniço Health Research and Training Center (CISPOC) at the Instituto Nacional de Saúde (INS)-Mozambique and the Kibong'oto Infectious Diseases Hospital-Tanzania.
Interventions
DRUGOptimised rifamycin
optimised dose rifampicin with or without moxifloxacin
Sponsors
University of St Andrews
Radboud University Medical Center
Stellah Mpagama
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Each patient must meet all the following inclusion criteria prior to enrolment into the trial: 1. The patient has given fully informed, signed written or witnessed oral informed consent for study participation prior to all trial-related procedures, including HIV testing if HIV status is not known. 2. The patient has a diagnosis of pulmonary TB established by Xpert MTB/RIF® result which confirms low medium or high level detection of M tuberculosis and does not detect rifampicin resistance. 1. If the patient has been referred from a clinic at which the pre-screening clinical diagnostic test for TB was an Xpert MTB/RIF® assay done at the trial laboratory, and the full read-out of that result is available, the test does not need to repeated to confirm eligibility. 2. If the patient has been referred from a clinic at which the pre-screening clinical diagnostic test for TB was an Xpert MTB/RIF® assay done at a non-trial laboratory, but the full read-out of that result is available, the test does not need to repeated to confirm eligibility. 3. If the patient has been referred to the study from a clinic from which the full pre-screening clinical diagnostic Xpert MTB/RIF® test result is unavailable, a repeat Xpert MTB/RIF® assay should be performed by the study laboratory to confirm eligibility before recruitment. 3. The patient should be aged ≥ 18 years on the day of providing informed consent. 4. The patient has a body weight in light clothing and without shoes of at least 35kg. 5. Female patients of child-bearing potential must have a negative urine or serum pregnancy test ≤ 7 days prior to screening, and consent to practice an effective method of contraception until completion of therapy. 6. The patient must have a verifiable residence location and telephone number that is accessible if necessary for contact during follow-up.
Exclusion criteria
* Patients for whom one of the following criteria is met will be excluded from the trial: 1. There is concern about any circumstances that raise concern about free, informed consent to study participation. 2. The patient's pre-screening or screening Xpert MTB/RIF® assay result is negative,trace, or very low positive. 3. At least one M tuberculosis isolate, either cultured or detected through molecular assays from sputum obtained from the patient prior to treatment initiation is found to be resistant to one or more of: rifampicin, isoniazid, pyrazinamide, ethambutol, or fluoroquinolones (late exclusion). 4. The patient is in poor general condition where delay in treatment cannot be tolerated, or death within three months is likely, as assessed by the investigator. 5. The patient had a nose/throat swab which was positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2), on Polymerase Chain Reaction (PCR) or a rapid diagnostic test ≤ 14 days preceding study recruitment. 6. The patient is pregnant or breast-feeding (female patients only). 7. The patient is unable to take oral medications. 8. The patient has received any investigational drug in the past three months. 9. The patient has received more than five days of treatment directed against active tuberculosis ≤ 6 months preceding initiation of study drugs. 10. The patient has known intolerance to any of the study drugs, or conditions for which they are contra-indicated. 11. The patient is unwilling, or unable to adhere to requirements regarding restricted use of other medications during the study. Restricted medications will include medications which prolong the QTc interval, and CYP450 inhibitors or inducers. 12. The patient is due to initiate, or requires continuation of, non-efavirenz, non-dolutegravir-based anti-retroviral therapy for HIV infection. 13. The patient has decompensated liver disease and/or aminotransaminases \>3x upper limit of normal (ULN), serum total bilirubin level \>1.5x ULN or serum/plasma creatinine level \>x2 ULN. 14. The patient has a baseline QTc interval of \>450ms. 15. The patient is being, or about to be, treated for malaria. 16. The patient has other medical conditions that, in the investigator's judgement, make study participation not in the individual's best interest.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Proportional of adverse events (AE) of grade 3 severity or higher | 4 or 6 months of treatment | The severity of all AEs will be classified according to the U.S. National Institutes of Health Common Terminology Criteria for Adverse Events 5.0 (CTCAE). |
| Bacteriological cure, absence of either TB treatment failure or relapse | Participant survival, free of tuberculosis 12 months after randomisation | Treatment failure, defined as submitting two sputum samples with positive culture for M tuberculosis on different visits, when the first of these samples was collected at or after two weeks prior to the scheduled end of treatment. TB relapse, defined as submitting two sputum samples with positive culture for M tuberculosis on different visits, when the first of these samples was collected after completion of scheduled TB therapy and where at least one of the M tuberculosis isolates is genetically similar to the baseline strain. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Clinical improvement of TB symptoms | 12 month after randomisation | Clinical response of TB symptoms as measured by questionnaire |
| Clinical improvement of participant reported health status | 12 month after randomisation | Increase of participant reported health status as measured by questionnaire |
| Clinical improvement of body mass index (BMI) | 12 month after randomisation | Increase of BMI as measured by the ratio of weight (kg) and height squared in metres squared |
| Proportional of clinically significant adverse events related to the intervention | 4 or 6 months of treatment | Treatment discontinuation or interruption related to AE |
Other
| Measure | Time frame | Description |
|---|---|---|
| Participant survival free of TB | 12 months after completing TB treatment | Recurrent of symptoms and bacteriological confirmation of TB |
Countries
Tanzania
Contacts
Primary ContactStellah Mpagama, PhD
Backup ContactAlphonce Liyoyo, M.D
Outcome results
None listed