ISENTRESS (raltegravir potassium)
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.
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
Details
- Status
- Prescription
- First Approved
- 2007-10-12
- Patent Cliff
- 2032
- Revenue
- $178M (Q4-2021)
- Routes
- ORAL
- Dosage Forms
- TABLET, CHEWABLE, POWDER, TABLET
ISENTRESS Approval History
What ISENTRESS Treats
1 indicationsISENTRESS 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
ISENTRESS Competitive Set
ProThree rings of competition based on shared molecular targets and treated indications.
Indication competitors
Same indication, different mechanism — what else might this patient receive?
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 10FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.
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 |
Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
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.
ISENTRESS Patents & Exclusivity
Patents (7 active)
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
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