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DRUG CLASS:

Non-nucleoside reverse transcriptase inhibitor

Related drugs:
2d
Enrollment open
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CD4 (CD4 Molecule)
4d
Trial completion
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efavirenz
6d
Analysis of Viral Blips Through Week 192 of the DRIVE-FORWARD and DRIVE-AHEAD Phase 3 Studies of Doravirine-Based Regimens in Adults Living With Previously Untreated HIV-1. (PubMed, Open Forum Infect Dis)
Adults living with untreated HIV-1 were randomized (1:1) to a DOR-containing regimen or comparator (darunavir/ritonavir- or efavirenz-containing), each with 2 nucleos(t)ide reverse transcriptase inhibitors, for 96 weeks (double-blind base), followed by 96 weeks of a DOR-containing regimen (open-label extension). Clinical Trials Registration.  ClinicalTrials.gov NCT02275780, NCT02403674.
Clinical • P3 data • Journal
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CD4 (CD4 Molecule)
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efavirenz
7d
LACRIS: Long-Acting Cabotegravir and Rilpivirine in People Living With HIV-1 Subtype A6: A Real-World Retrospective Study (clinicaltrials.gov)
P=N/A, N=250, Recruiting, Pomeranian Medical University Szczecin | Not yet recruiting --> Recruiting | Trial completion date: Feb 2026 --> Mar 2027 | Initiation date: Feb 2026 --> May 2026 | Trial primary completion date: Feb 2026 --> Feb 2027
Enrollment open • Trial completion date • Trial initiation date • Trial primary completion date • Real-world evidence
9d
CREATE: Cabotegravir & Rilpivirine Antiretroviral Therapy in Pregnancy (clinicaltrials.gov)
P=N/A, N=40, Not yet recruiting, International Maternal Pediatric Adolescent AIDS Clinical Trials Group
New trial
13d
The Effect of Efavirenz and Rufinamide on the Pharmacokinetics and Safety of Quizartinib: Two Phase 1 Studies in Healthy Participants. (PubMed, Clin Transl Sci)
These results suggest that concomitant use of quizartinib and moderate CYP3A inducers should be avoided. Concomitant use of weak CYP3A inducers does not warrant dose adjustment, since the impact on quizartinib exposure is clinically nonrelevant.
P1 data • PK/PD data • Journal
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FLT3 (Fms-related tyrosine kinase 3)
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Vanflyta (quizartinib) • efavirenz
20d
Interaction of CYP2B6 Genotype and Efavirenz With Methadone and Tizanidine PK (clinicaltrials.gov)
P1, N=60, Recruiting, Indiana University | Trial completion date: Apr 2027 --> Dec 2026 | Trial primary completion date: Apr 2027 --> Aug 2026
Trial completion date • Trial primary completion date
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efavirenz
24d
Interaction of CYP2B6 Genotype and Efavirenz With Methadone and Tizanidine PK (clinicaltrials.gov)
P1, N=60, Recruiting, Indiana University | Trial completion date: Apr 2026 --> Apr 2027 | Trial primary completion date: Apr 2026 --> Apr 2027
Trial completion date • Trial primary completion date
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efavirenz
27d
Study of KM-023 in Healthy Volunteers and Patients With Olmsted Syndrome. (clinicaltrials.gov)
P1, N=64, Recruiting, Orvida Pharma (formerly Kamari Pharma) | Trial completion date: Feb 2026 --> Nov 2026 | Trial primary completion date: Feb 2026 --> Nov 2026
Trial completion date • Trial primary completion date
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TRPV3 (Transient Receptor Potential Cation Channel Subfamily V Member 3)
1m
TMC125-TiDP35-C239 - Continued Access to Etravirine (ETR) in Treatment Experienced HIV-1 Infected Participants (clinicaltrials.gov)
P3, N=180, Completed, Janssen Sciences Ireland UC | Active, not recruiting --> Completed
Trial completion