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Recruiting Phase 2 NCT07517445

Bactericidal Activity and Safety of Nicotinamide in Combination With Bedaquiline, Pretomanid, and Linezolid in Drug-susceptible Pulmonary Tuberculosis

Phase 2 – studying effectiveness and dosage
Conditions: Drug Susceptible Pulmonary Tuberculosis

Sponsor: Gates Medical Research Institute

trial.available_in: БГ
Overview
The purpose of this study is to determine if nicotinamide in combination with bedaquiline, pretomanid, and linezolid, is safe and effective in treating drug-susceptible pulmonary tuberculosis.
Who can participate
Inclusion Criteria: * Age 18-65 years at consent * Body weight 40-100 kg at screening * Written informed consent obtained * Newly diagnosed pulmonary TB, rifampicin- and isoniazid-sensitive * ≥1+ AFB smear OR positive Xpert semi-quantitative result * Molecular confirmation of M. tuberculosis * Chest X-ray consistent with TB (Investigator assessment) * Able to spontaneously produce sputum * Contraception requirements met * Females Of Child Bearing Potential: 2 approved contraceptive methods or abstinence * Males: contraception or abstinence through 90 days post-dose Exclusion Criteria: * Prior TB within 3 years, \>1 prior episode, or anti-TB treatment within 60 days * Extrapulmonary TB (except non-significant pleural/lymph node disease) * Clinically significant comorbidities or substance abuse impacting safety/compliance * Pregnant or breastfeeding * HIV-positive AND any of the following: * Not on ART or on ART \<3 months * CD4 \<200 cells/µL * Viral load \>200 copies/mL * AIDS-defining illness (other than pulmonary TB) * Screening lab abnormalities (protocol-defined LFTs, hematology, hepatitis B or C, HbA1c) * Clinically significant ECG abnormality * Use of prohibited concomitant medications (e.g., strong CYP3A4 modifiers, certain SSRIs)
Interventions
Bedaquiline, pretomanid, linezolid
DRUG
Bedaquiline, pretomanid, linezolid
DRUG
Bedaquiline, pretomanid, linezolid
DRUG
Nicotinamide (NAM)
DIETARY_SUPPLEMENT
Locations 4
South Africa (4)
TASK Clinical Research Centre
Cape Town , Western Cape
Centre of Tuberculosis Research Innovation
Cape Town , Western Cape
NOT_YET_RECRUITING
Wits RHI - Shandukani Research
Johannesburg , Gauteng
NOT_YET_RECRUITING
The Aurum Institute Clinical Research Site - Pretoria
Pretoria , Gauteng
NOT_YET_RECRUITING
Technical details
Status
Recruiting
Phase
Phase 2
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
13.04.2026
Completion date
14.06.2027
Registry ID
NCT07517445
Source
clinicaltrials.gov
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