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rifampin

Generic: RIFAMPIN·Brand: RIFADIN, RIFAMPIN, RIMACTANE, Rifadin

rifampin: 16 clinical trials tracked.

rifampin evidence translation

What we can confirm

16 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about rifampin, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence6 indications · 5 study sponsors
Clinical Trial Registry Records (16)showing 10 most recent

An Open-label, Phase 1 Study to Characterize the Effects of Rifampin on the Pharmacokinetics of MK-8527 in Adult Participants With Latent Tuberculosis Infection

NCT07600775Registry updated 2026-08-03·Phase 1
Not yet recruiting

Primary endpoint: Area Under the Concentration-Time Curve From Time Zero to Infinity (AUC0-inf) of MK-8527

Interventionalopen14 targetStarted 2026-09Completion 2027-01Merck Sharp & Dohme LLC

A Phase 1, Open-label, Randomized, Pharmacokinetic Study to Assess the Drug Interactions and Food Effect of Navlimetostat (BMS-986504) in Healthy Female Participants

NCT07800897Registry updated 2026-10-05·Phase 1·BMY
Recruiting

Primary endpoint: Maximum observed concentration (Cmax) of Navlimetostat

Interventionalopen80 targetStarted 2026-08Completion 2027-031 site · CanadaBristol-Myers Squibb

Optimal Treatment Duration for Radiographically Apparent, Bacteriologically Unconfirmed TB, Identified Through Active Case Finding

NCT07163143Registry updated 2025-09-09·Phase 3
Not yet recruiting

Primary endpoint: Proportion of participants with an unfavourable TB outcome

InterventionalRandomizedopen784 targetStarted 2025-11Completion 2029-044 sites · Pakistan, South Africa, ZimbabweUniversity College, London

An Open-Label Study to Assess the Effect of Itraconazole, Rifampin, and Acid-Reducing Agents on INCB161734 Pharmacokinetics When Administered Orally in Healthy Participants

NCT07018635Registry updated 2025-11-26·Phase 1·INCY
Completed

Primary endpoint: Pharmacokinetics Parameter (PK): Cmax of INCB161734

Interventionalopen63 enrolledStarted 2025-07Completion 2025-091 site · United StatesIncyte Corporation

Shortened Regimen for Drug-susceptible TB in Children

NCT06253715Registry updated 2026-07-24·Phase 3
Recruiting

Primary endpoint: TB disease-free survival at 48-weeks

InterventionalRandomizedopen860 targetStarted 2025-01Completion 2027-099 sites · India, Indonesia, Mozambique, South Africa…Johns Hopkins University

Co-SAM: An Adaptive Multi-arm Trial to Improve Clinical Outcomes Among Children Recovering From Complicated Severe Acute Malnutrition

NCT05994742Registry updated 2026-08-25·Phase 3
Completed

Primary endpoint: Death or first hospitalisation or failed nutritional recovery within 24 weeks post-randomisation

InterventionalRandomizedopen674 enrolledStarted 2024-07Completion 2026-079 sites · Kenya, Zambia, ZimbabweQueen Mary University of London

A Phase IIc, Open-Label, Randomized Controlled Trial of Ultra-Short Course Bedaquiline, Clofazimine, Pyrazinamide and Delamanid Versus Standard Therapy for Drug-Susceptible Tuberculosis (PRESCIENT)

NCT05556746Registry updated 2026-02-11·Phase 2
Active, not recruiting

Primary endpoint: Time to stable liquid culture conversion

InterventionalRandomizedopen156 targetStarted 2023-11Completion 2027-012 sites · Haiti, South AfricaBrigham and Women's Hospital

A Phase 1, Open Label, Fixed Sequence Study to Assess the Pharmacokinetics of Brensocatib When Administered Alone and With Multiple Doses of Rifampin (CYP3A Inducer) or Esomeprazole (Proton Pump Inhibitor) in Healthy Subjects

NCT05826574Registry updated 2023-08-21·Phase 1·INSM
Completed

Primary endpoint: Parts 1 and 2: Area Under the Concentration-time (AUC) of Brensocatib in Plasma

Interventionalopen32 enrolledStarted 2023-05Completion 2023-071 site · United StatesInsmed Incorporated

A Multicenter, Phase 2b/c, Open-label, Randomized, Dose-finding Trial to Evaluate the Safety and Efficacy of a 4 Month Regimen of OPC-167832 in Combination With Delamanid and Bedaquiline in Subjects With Drug-susceptible Pulmonary Tuberculosis in Comparison With Standard Treatment

NCT05221502Registry updated 2026-08-12·Phase 2
Completed

Primary endpoint: Number of Participants With Treatment-Emergent Adverse Events (TEAEs), Serious TEAEs, Severe TEAEs, TEAEs Related to Study Drug, TEAEs Leading to Study Discontinuation, TEAEs Leading to Death, and All Grade TEAEs Based on DAIDS Criteria

InterventionalRandomizedopen122 enrolledStarted 2022-04Completion 2024-056 sites · South AfricaOtsuka Pharmaceutical Development & Commercialization, Inc.

Multi-centric Prospective Cohort Study of TB Recurrence Free Cure Among Microbiologically Confirmed New Pulmonary Tuberculosis Patients Treated Under NTEP With the 4-month Moxifloxacin Containing Daily Regimen

NCT05047055Registry updated 2026-09-16
Completed

Primary endpoint: TB recurrence free cure

Observational550 enrolledStarted 2022-03Completion 2026-041 site · IndiaTuberculosis Research Centre, India