TheraRadar
Data updated: May 26, 2026

VIRAMUNE XR (nevirapine)

Infectious Disease Approved 2011-03-25
3
Indications
--
Phase 3 Trials
15
Years on Market

Details

Status
Discontinued
First Approved
2011-03-25
Patent Cliff
2029

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Routes
ORAL
Dosage Forms
TABLET, EXTENDED RELEASE

Companies

Active Ingredient: NEVIRAPINE

VIRAMUNE XR Approval History

2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
20 FDA actions from 2011 to 2024 · 2 indication expansions
Jul 2024 SUPPL
Label · Labeling
Jun 2022 SUPPL
Label · Labeling
Sep 2018 SUPPL
Label · Labeling

What VIRAMUNE XR Treats

3 FDA approvals

Originally approved for its first indication in 2011 . Covers 3 distinct patient populations.

  • Other (3)
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Clinical Trial Registry

12 trials
Trial Sponsor ID Phase Status Title
NCT02369406 EIT U01AI114235 Ph 2, Ph 3 active not recruiting Early Infant HIV Treatment in Botswana
NCT01789879 0022-14-EP 1R21HD074462-01 Ph 2 completed A Pharmacokinetic Evaluation of Levonorgestrel Implant and Antiretroviral Therapy
NCT02712801 2015ZX10001001 Ph 4 completed Antiretroviral Regime for Viral Eradication in Newborns
NCT03088410 IRB 2019-2922 R01DK109881, HRDC 00781 Ph 4 completed Study of HIV-Infected and Uninfected Pregnant Woman/Child Dyads in Gaborone, Botswana
NCT00672412 P1069 10620, IMPAACT P1069 Ph 1, Ph 2 completed Safety and Pharmacokinetic Study of Fixed Dose Combination of Zidovudine, Lamivudine, and Nevirapine in HIV-Infected Children in Thailand
NCT02431975 LEOPARD AAAO5011 U01HD080441 Ph 4 completed Latency and Early Neonatal Provision of Antiretroviral Drugs Clinical Trial
NCT00661349 A10-174 (KANELA) Ph 4 terminated Trial About Hepatic Security of Antiretroviral Treatment Based on Kaletra Versus Nevirapine in Co-infected HIV/HCV Patients
NCT01632891 results posted ACTG A5297 1U01AI068636 Ph 1, Ph 2 completed Comparing PI-Based to a nNRTI-based ART for Clearance of Plasmodium Falciparum Parasitemia in HIV-Infected
NCT02116660 RANIA results posted 0518-284 2013-001637-40, MK-0518-284 Ph 2 terminated Evaluation of Renal Function, Efficacy, and Safety When Switching From Tenofovir/Emtricitabine Plus a Protease Inhibitor/Ritonavir, to a Combination of Raltegravir (MK-0518) Plus Nevirapine Plus Lamivudine in HIV-1 Participants With Suppressed Viremia and Impaired Renal Function (MK-0518-284)
NCT01637558 DATiC DATiC Ph 4 completed Optimal Dosing of 1st Line Antituberculosis and Antiretroviral Drugs in Children (a Pharmacokinetic Study)
NCT02202005 NEVIR5U14EU 2014-002247-18 Ph 1 completed Multiple Dose BE Study With Nevirapine 400mg PR Tablets
NCT01772940 Lubumbashi trial Ph 4 completed Nevirapine vs Ritonavir-boosted Lopinavir in ART Naive HIV-infected Adults in a Resource Limited Setting
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

VIRAMUNE XR FDA Label Details

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1 OB patents · 1 families · 41 international docs across 29 countries

VIRAMUNE XR Patents & Exclusivity

Latest Patent: Mar 2029

Patents (1 active)

US8460704 Expires Mar 12, 2029
Source: FDA Orange Book

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Revenue Insights

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Patent Timeline

  • Cliff: 2029
  • 2 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

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  • Same target/indication analysis
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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.