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efavirenz

Generic: EFAVIRENZ·Brand: Atripla, EFAVIRENZ, SUSTIVA, Sustiva, Symfi

efavirenz: 7 clinical trials tracked.

efavirenz evidence translation

What we can confirm

7 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 efavirenz, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence4 indications · 2 study sponsors
Clinical Trial Registry Records (7)

The Drug-Drug Interaction Study of Clifutinib

NCT07341672Registry updated 2026-04-27·Phase 1
Not yet recruiting

Primary endpoint: Cmax

InterventionalRandomizedopen80 targetStarted 2026-12Completion 2027-051 site · ChinaSunshine Lake Pharma Co., Ltd.

A Phase 1, Open-label Drug-drug Interaction Study to Evaluate the Effects of Efavirenz on the Pharmacokinetics of Suzetrigine in Healthy Subjects

NCT07570069Registry updated 2026-08-18·Phase 1
Completed

Primary endpoint: Maximum Observed Plasma Concentration (Cmax) of SUZ and its Metabolite in the Absence and Presence of Efavirenz

Interventionalopen18 enrolledStarted 2026-05Completion 2026-071 site · United StatesVertex Pharmaceuticals Incorporated

A Phase I, Randomized, Open-label, Drug-drug Interaction Study to Assess the Effect of Multiple Doses of a Moderate and a Strong CYP3A Inducer on the Pharmacokinetics and Safety of Mavorixafor in Healthy Male and Female Participants

NCT06914869Registry updated 2025-07-01·Phase 1·XFOR
Completed

Primary endpoint: Cohort 1: Maximum Observed Plasma Concentration (Cmax) of Mavorixafor Without (Day 1) and With (Day 18) Coadministration With Carbamazepine

InterventionalRandomizedopen38 enrolledStarted 2025-02Completion 2025-051 site · United StatesX4 Pharmaceuticals

A Single Sequence, 2-Period, Open-label Crossover Study in Healthy Subjects to Determine the Effect of a Moderate CYP3A4 Inducer on the Pharmacokinetics of Omaveloxolone

NCT05909644Registry updated 2025-05-30·Phase 1·BIIB
Completed

Primary endpoint: Maximum concentration (Cmax) of omaveloxolone

Interventionalopen20 enrolledStarted 2023-07Completion 2023-081 site · United StatesBiogen

Pilot Trial Evaluating Once Daily Triple Combination Antiretroviral Therapy With Tenofovir-Emtricitabine and Efavirenz in HIV-1 Infected Patients With Mycobacterium Tuberculosis Infection ANRS129 BKVIR

NCT00115609Registry updated 2026-04-08·Phase 3
Completed

Primary endpoint: treatment success rate at week 48 (W48)

Interventionalopen70 enrolledStarted 2006-01Completion 2009-111 site · FranceFrench National Agency for Research on AIDS and Viral Hepatitis

Phase II Randomized Trial Comparing Efficacy and Safety of the Maintenance of a HAART Association Protease Inhibitor Containing Versus a Once Daily Antiretroviral Triple Association, in HIV Adult Patients With Undetectable Viral Load.ANRS 099 ALIZE

NCT00196612Registry updated 2026-06-15·Phase 3
Completed

Primary endpoint: Virological success from W0 to W48

InterventionalRandomizedopen350 enrolledStarted 2001-04Completion 2004-091 site · FranceANRS, Emerging Infectious Diseases

Pilot Study on Efficacy and Safety of a Once Daily FTC, ddI, Efavirenz Combination in Antiretroviral Naive HIV Infected Adults. ANRS 091 MONTANA

NCT00196599Registry updated 2026-06-15·Phase 2
Completed

Primary endpoint: Virological success

Interventionalopen39 enrolledStarted 1999-02Completion 2004-091 site · FranceANRS, Emerging Infectious Diseases