TheraRadar
Data updated: May 26, 2026

ISENTRESS (raltegravir potassium)

Trial Activity: Declining
Infectious Disease Approved 2007-10-12

Isentress (raltegravir) is indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection in patients 4 weeks of age and older. Clinical efficacy is optimized when Isentress is used as part of a multi-drug regimen containing other active agents, which is associated with a greater likelihood of virologic response.

Source: FDA Label • Merck

How ISENTRESS Works

Raltegravir is an HIV-1 integrase strand transfer inhibitor (INSTI). It works by inhibiting the catalytic activity of HIV-1 integrase, an enzyme required for viral replication. By blocking this enzyme, raltegravir prevents the covalent insertion (integration) of the HIV-1 DNA into the host cell genome, thereby preventing the formation of the HIV-1 provirus and the propagation of the viral infection.

Development Insights

ANRS, Emerging Infectious Diseases conducting 1 trials (33%)
7 indications explored (Moderate)
hiv infection (1 trials)
liver failure (1 trials)
evidence of liver transplantation (1 trials)
13
Indications
--
Phase 3 Trials
4
Priority Reviews
18
Years on Market

Details

Status
Prescription
First Approved
2007-10-12
Patent Cliff
2032
Revenue
$178M (Q4-2021)

Pro Metrics

Patent cliff and revenue data

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Routes
ORAL
Dosage Forms
TABLET, CHEWABLE, POWDER, TABLET

Companies

Active Ingredient: RALTEGRAVIR POTASSIUM

ISENTRESS Approval History

2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
77 FDA actions from 2007 to 2021 · 10 indication expansions
May 2021 SUPPL
Label · Labeling
Jul 2020 SUPPL
Efficacy
Jun 2018 SUPPL
Label · Labeling

What ISENTRESS Treats

1 indications

ISENTRESS is approved for 1 conditions since its original approval in 2007. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Human Immunodeficiency Virus
Source: FDA Label

ISENTRESS Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to ISENTRESS

3 of 10

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

BIKTARVY
BICTEGRAVIR SODIUM
1 shared
Gilead Sciences
Shared indications:
DARUNAVIR
DARUNAVIR
1 shared
Teva
Shared indications:
EMTRICITABINE, RILPIVIRINE AND TENOFOVIR DISOPROXIL FUMARATE
EMTRICITABINE
1 shared
Viatris
Shared indications:
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Clinical Trial Registry

1 trials
Trial Sponsor ID Phase Status Title
NCT01022476 LIVERAL ANRS 148 LIVERAL 2009-014616-36 Ph 1, Ph 2 completed Raltegravir in Patients With End Stage Liver Disease and in Transplant Recipients
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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.

ISENTRESS FDA Label Details

Indications & Usage

FDA Label (PDF)

ISENTRESS is indicated for the treatment of Human Immunodeficiency Virus.

View full patent landscape →
7 OB patents · 4 families · 155 international docs across 42 countries

ISENTRESS Patents & Exclusivity

Latest Patent: Mar 2032

Patents (7 active)

US10772888 Expires Mar 30, 2032
US9649311*PED Expires Apr 21, 2031
US9649311 Expires Oct 21, 2030
US8771733 Expires Jun 2, 2030
US7754731*PED Expires Sep 11, 2029
US7754731 Expires Mar 11, 2029
US8852632 Expires Jan 28, 2028
Source: FDA Orange Book

Pro Intelligence Preview

Deep insights for ISENTRESS

Revenue Insights

  • Q4-2021: $178M
  • Historical trend analysis

Patent Timeline

  • Cliff: 2032
  • 22 active patents

Trial Analysis

  • 3 total trials
  • Stage: Declining

Competitive Landscape

  • 10 similar drugs
  • Same target/indication analysis
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Full approval history • All patents • Revenue trends • Competitor analysis

Data Sources

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

How We Calculate These Metrics

Trial Activity Stage

Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.

Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.

  • Growth: High proportion of early-phase trials (Phase 1/2), active development
  • Expansion: Significant Phase 3 activity, approaching or pursuing approvals
  • Mature: Substantial Phase 4 post-marketing studies
  • Stable: Mixed phase distribution, steady development
  • Declining: Low active trial ratio, reduced R&D investment