Active Ingredient History
Bictegravir is a component of the fixed-dose combination product bictegravir/emtricitabine/tenofovir alafenamide (BIKTARVY®), which received marketing approval for the treatment of human immunodeficiency virus (HIV) infection by the U.S. Food and Drug Administration in February 2018. Bictegravir inhibits the strand transfer activity of HIV-1 integrase, an HIV-1 encoded enzyme that is required for viral replication. Inhibition of integrase prevents the integration of linear HIV-1 DNA into host genomic DNA, blocking the formation of the HIV-1 provirus and propagation of the virus. NCATS
Combination drugs
Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Alveolar Bone Loss (Phase 4)
Antiretroviral Therapy, Highly Active (Phase 4)
Art (Phase 4)
Bone Diseases, Metabolic (Phase 4)
Buprenorphine (Phase 4)
Coinfection (Phase 4)
Coronary Artery Disease (Phase 4)
Drug Misuse (Phase 4)
Harm Reduction (Phase 4)
Healthy Volunteers (Phase 1)
Hepatitis B (Phase 4)
Hepatitis C (Phase 4)
Hepatitis C, Chronic (Phase 4)
HIV (Phase 4)
HIV-1 (Phase 4)
HIV Seropositivity (Phase 3)
Kidney Transplantation (Phase 4)
Methadone (Phase 4)
Opioid-Related Disorders (Phase 4)
Sexually Transmitted Diseases (Phase 4)
Tuberculosis (Phase 4)
Tuberculosis, Pulmonary (Phase 2)
Trial | Phase | Start Date | Organizations | Indications |
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