Emtricitabine/rilpivirine/tenofovir
Combination of |
Emtricitabine |
Nucleoside analog reverse-transcriptase inhibitor |
Rilpivirine |
Non-nucleoside reverse transcriptase inhibitor |
Tenofovir disoproxil fumarate |
Nucleoside analog reverse-transcriptase inhibitor |
Clinical data |
Legal status |
℞-only (US) ℞ Prescription only |
Routes |
Oral |
Identifiers |
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ATC code |
J05AR08 |
Y (what is this?) (verify) |
Emtricitabine/rilpivirine/tenofovir (trade name Complera, Eviplera) is a fixed dose combination of antiretroviral drugs for the treatment of HIV.[1] The drug was co-developed by Gilead Sciences and Johnson & Johnson's Tibotec division and was approved by the Food and Drug Administration in August 2011, and by the European Medicines Agency in November 2011 (Eviplera),[2] for patients who have not previously been treated for HIV.[3] It is available as a once-a-day single tablet.
References
Antiviral drugs: antiretroviral drugs used against HIV (primarily J05) |
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| Entry/fusion inhibitors (Discovery & development) |
- gp41 (Enfuvirtide)
- CCR5 (Maraviroc
- Vicriviroc†, Cenicriviroc†, PRO 140†)
- CD4 (Ibalizumab†)
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| Reverse-transcriptase inhibitors (RTIs) |
Nucleoside & nucleotide (NRTI) |
- Nucleoside analogues/NARTIs: Abacavir (ABC)°#
- Emtricitabine (FTC)°#
- Lamivudine (3TC)°#
- Didanosine (ddI)#
- Zidovudine (AZT)#
- Apricitabine†
- Stampidine†
- Elvucitabine†
- Racivir†
- Amdoxovir†
- Stavudine (d4T)#
- Zalcitabine (ddC)◊
- Festinavir†
- Nucleotide analogues/NtRTIs: Tenofovir disoproxil fumarate (TDF)°#
- Tenofovir alafenamide fumarate (TAF)†
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| Non-nucleoside (NNRTI) (Discovery & development) |
- (1st generation) Efavirenz (EFV)°#
- Nevirapine (NVP)#
- Loviride◊
- Delavirdine (DLV)◊
-
(2nd generation) diarylpyrimidines (Etravirine
- Rilpivirine)
- Lersivirine†
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| Integrase inhibitors |
- Raltegravir°
- Elvitegravir
- Dolutegravir
- Globoidnan A (experimental)
- MK-2048†
- BI 224436†
- GSK744†
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| Maturation inhibitors | |
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| Protease Inhibitors (PI) (Discovery and development) |
1st generation |
- Fosamprenavir°
- Lopinavir°#
- Nelfinavir#
- Ritonavir#
- Saquinavir#
- Amprenavir◊
- Indinavir◊#
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| 2nd generation |
- Atazanavir°
- Darunavir°
- Tipranavir
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| Combined formulations |
- Lamivudine/zidovudine
- Emtricitabine/tenofovir/efavirenz
- Abacavir/lamivudine/zidovudine
- Tenofovir/emtricitabine
- Lopinavir/ritonavir
- Abacavir/lamivudine
- Emtricitabine/rilpivirine/tenofovir
- Elvitegravir/cobicistat/emtricitabine/tenofovir
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| Experimental agents |
Uncoating inhibitors | |
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| Transcription inhibitors | |
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| Translation inhibitors | |
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| Other |
- Abzyme
- Calanolide A
- Ceragenin
- Cyanovirin-N
- Diarylpyrimidines
- Epigallocatechin gallate (EGCG)
- Foscarnet
- Griffithsin
- Hydroxycarbamide
- Miltefosine
- Portmanteau inhibitors
- Seliciclib†
- Synergistic enhancers
- Tre recombinase
- Zinc finger protein transcription factor
- KP-1461†
- Cobicistat†
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| Failed agents |
- Dexelvucitabine
- Capravirine
- Emivirine
- Lodenosine
- Atevirdine
- Brecanavir
- Aplaviroc
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
°DHHS preferred first-line agent. ◊Formerly or rarely used agent.
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cutn/syst (hppv/hiva, infl/zost/zoon)/epon
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drug (dnaa, rnaa, rtva, vacc)
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