TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ISENTRESS

RALTEGRAVIR POTASSIUM
Infectious Disease Approved 2007-10-12
13
Indications
--
Phase 3 Trials
4
Priority Reviews
18
Years on Market

Details

Status
Prescription
First Approved
2007-10-12
Routes
ORAL
Dosage Forms
TABLET, TABLET, CHEWABLE, POWDER

Companies

Active Ingredient: RALTEGRAVIR POTASSIUM

ISENTRESS Approval History

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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
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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

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Indications & Usage

FDA Label (PDF)

ISENTRESS® is indicated in combination with other antiretroviral agents for the treatment of human immunodeficiency virus (HIV-1) infection in patients 4 weeks of age and older. The use of other active agents with ISENTRESS is associated with a greater likelihood of treatment response [see Clinical Studies ] . ISENTRESS is a human immunodeficiency virus integrase strand transfer inhibitor (HIV-1 INSTI) indicated: In combination with other antiretroviral agents for the treatment of HIV-1 infection in patients 4 weeks of age and older . The use of other active agents with ISENTRESS is associated...

ISENTRESS Patents & Exclusivity

Latest Patent: Mar 2032

Patents (22 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
+ 12 more patents
Source: FDA Orange Book

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Data Sources

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