HIV-1-infection, Immuno-Deficiency, Tuberculosis
Conditions
Keywords
Tuberculosis, HIV-1, Mortality, Immuno-deficiency, Isoniazid, Rifampicin
Brief summary
DATURA trial is a phase III, multicenter, two-arm, open-label, randomized superiority trial to compare the efficacy and the safety of an intensified tuberculosis (TB) regimen versus standard TB treatment in HIV-infected adults and adolescents hospitalized for TB with CD4 ≤ 100 cells/μL over 48 weeks: * Intensified TB treatment regimen: increased doses of rifampicin and isoniazid together with standard-dose of pyrazinamide and ethambutol for 8 weeks in addition to prednisone for 6 weeks and albendazole for 3 days * WHO standard TB treatment regimen. The continuation phase of TB treatment will be identical in the two arms: 4 months of rifampicin and isoniazid at standard doses.
Detailed description
Settings: 5 African (Cameroon, Guinea, Uganda, Zambia, Mozambique) and 1 South-East Asian (Cambodia) countries. Sample size : 1330 patients (665 in each arm). Follow-up : 48 weeks after entry in the trial (TB treatment initiation). All participants will initiate antiretroviral therapy (ART) 2 weeks after starting TB treatment. In each country, the chosen ART regimen will be the same in both arms. According to the first-line regimen recommended in each country, the ART combination will be TDF/3TC/EFV 600 mg, or TDF/3TC + double-dose DTG. The primary objective is to estimate the impact of an intensified initial phase of TB treatment on mortality at 48 weeks among HIV-infected adults and adolescents hospitalized for TB with CD4 ≤ 100 cells/μL in comparison with standard TB treatment. The secondary objectives are to estimate the impact of an intensified initial phase of TB treatment, in comparison with the standard TB regimen, on: * Mortality at weeks 8 and 24 * Adverse events, including * All grade 3 and 4 events * Selected grade 2 events of interest * Drug-related adverse events * AIDS-defining illnesses * Paradoxical TB-associated immune reconstitution inflammatory syndrome (IRIS) * TB treatment success * TB recurrence * ART response in terms of virological success and immunological response * Adherence to TB treatment and ART * Peak plasma concentrations of rifampicin and isoniazid (and its N-acetyl-metabolite) at day 3, day 7 and week 2 * Plasma concentrations of efavirenz and dolutegravir at week 4 (i.e. 2 weeks after the onset of ART). A pharmacokinetic sub-study of rifampicin and isoniazid will be carried out in 72 voluntary patients (6 patients/arm/country) at the second week of the main study.
Interventions
DRUGIntensified TB treatment (initial phase)
8 weeks of RHEZ with high dose of rifampicin (R) and isoniazid (H). Fixed dose combination (FDC) of RHZE with the addition of FDC of RH and single caps of R. 6 weeks of prednisone with tapering doses. 3 days of albendazole 400 mg.
DRUGWHO standard TB treatment (initial phase)
8 weeks of RHEZ with FDC.
Sponsors
European Union
European and Developing Countries Clinical Trials Partnership (EDCTP)
ANRS, Emerging Infectious Diseases
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
DATURA trial is a phase III, multicenter, two-arm, open-label, randomized superiority trial.
Eligibility
Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patient (and legally designed representative of minor patient) able to correctly understand the trial and to sign the informed consent * Aged ≥ 15 years * Confirmed HIV-1 infection as documented at any time prior to trial entry per national HIV testing procedures * CD4 count ≤ 100 cells/μL * Hospitalized for a newly diagnosed TB, defined by: * Any positive Xpert® MTB/RIF specimen (sputum, urine, pus, other), * Or a positive urine lipoarabinomannan (LAM) test, * Or an abnormal chest X-ray compatible with active TB EXCLUSION CRITERA * Initiation of TB drugs for more than 7 days * History of TB treatment during the last 6 months * Central neurological symptoms, including but not restrictive to TB meningitis * Suspected TB pericarditis * Documented Mycobacterium tuberculosis strain resistant to rifampicin using rapid molecular testing (Xpert® MTB/RIF) * Any concomitant medication or known hypersensitivity contraindicating any component of the TB treatment * HIV-2 co-infection * Current treatment with ART containing protease inhibitors * Any contraindication to efavirenz and dolutegravir * Severe associated diseases requiring corticosteroids or for which corticosteroids are contra-indicated * Impaired hepatic function with ALT (SGPT) \> 5 times the upper limit of normal (ULN) value * Creatinine clearance \< 30 mL/min/1.73m2 (according to either the MDRD or the CKD-EPI formula) * Pregnancy or breastfeeding
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of all causes death | Up to 48 weeks | Number of deaths between the inclusion visit and week 48, divided by the total person-years of follow-up until week 48 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Rate of all causes death | Up to 8 weeks | Death for any cause at week 8 will be calculated as the number of deaths between the inclusion visit and week 24, divided by the total person-years of follow-up during the same period |
| Rate of adverse events | Up to 48 weeks | Number of serious adverse events, all grade 3-4 adverse events (using the DAIDS tables), and any grade 2 adverse events of interest (e.g., hepatotoxicity, rash, peripheral neuropathy, thrombocytopenia, neuropsychiatric disorders), between the inclusion visit and week 48, divided by the total person-years of follow-up during that period |
| Rate of AIDS-defining illnesses | Up to 48 weeks | Number of AIDS-defining illnesses according to the WHO clinical staging table |
| Rate of paradoxical TB-associated IRIS | Up to 14 weeks | Number of paradoxical TB-associated IRIS according to the definition of the international network for the study of HIV-associated (INSHI) consensus case definition |
| Rate of TB treatment success | Up to 24 weeks | The percentage of patients with TB success will be calculated as the number of patients who are cured or who have completed TB treatment, as defined by WHO, divided by the total number of randomized patients |
| Plasma concentrations of rifampicin and isoniazid | Up to 2 weeks | Determined 2 hours after the TB drugs intake at day 3, day 7 and week 2 in a subset of 20 patients per arm per country |
| Rate of virological success | Week 24 | The percentage will be calculated as the number of patients with HIV RNA \<50 copies/mL divided by the total number of randomized patients. |
| Adherence to TB and ART treatment | up to 24 weeks | The proportion of days with perfect adherence divided by the total number of days of treatment |
| Immunological response | Up to 48 weeks | The mean CD4 cell count gain (with 95% confidence interval) will be calculated as the difference of CD4 cell count between pre-inclusion and week 48 |
| Plasma concentrations of efavirenz and dolutegravir | Week 4 | Determined 12 hours after the drugs intake at week 4 (i.e. 2 weeks after the onset of ART) in a subset of 60 patients per arm for efavirenz and 60 patients per arm for dolutegravir |
| Rate of TB recurrence | Up to 48 weeks | The number of patients with TB recurrence divided by the total number of randomized patients with TB treatment success at week 24 |
Countries
Cambodia, Cameroon, Guinea, Mozambique, Uganda, Zambia
Outcome results
None listed