TheraRadar
Data updated: May 26, 2026

APTIVUS (tipranavir)

HIV Protease Inhibitors Trial Activity: Declining
Infectious Disease Approved 2005-06-22

APTIVUS is indicated for the treatment of HIV-1 Infection.

Source: FDA Label • Boehringer Ingelheim • Protease Inhibitor

How APTIVUS Works

Tipranavir is a non-peptidic protease inhibitor (PI) that targets the HIV-1 protease enzyme. By binding to the active site of the enzyme, it inhibits the cleavage of viral Gag and Gag-Pol polyproteins into the functional proteins required for infectious virion assembly. This results in the production of immature, non-infectious viral particles. Co-administration with ritonavir is required to inhibit CYP3A4 metabolism and increase tipranavir plasma concentrations.

Development Insights

Boehringer Ingelheim conducting 2 trials (67%)
2 indications explored (Focused)
healthy (2 trials)
hiv infections (1 trials)
3
Indications
--
Phase 3 Trials
2
Priority Reviews
20
Years on Market

Details

Status
Prescription
First Approved
2005-06-22
Routes
ORAL
Dosage Forms
SOLUTION, CAPSULE

Companies

Active Ingredient: TIPRANAVIR

APTIVUS Approval History

2006
2007
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
29 FDA actions from 2005 to 2024 · 1 indication expansions
Apr 2024 SUPPL
Label · Labeling
Jun 2020 SUPPL
Label · Labeling
Jun 2018 SUPPL
Label · Labeling

What APTIVUS Treats

1 indications

APTIVUS is approved for 1 conditions since its original approval in 2005. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • HIV-1 Infection
Source: FDA Label

APTIVUS Boxed Warning

HEPATOTOXICITY and INTRACRANIAL HEMORRHAGE WARNING: HEPATOTOXICITY and INTRACRANIAL HEMORRHAGE See full prescribing information for complete boxed warning. Clinical hepatitis and hepatic decompensation including some fatalities. Extra vigilance is warranted in patients with chronic hepatitis B or hepatitis C co-infection. ( 5.2 ) Fatal and non-fatal intracranial hemorrhage ( 5.3 ) Hepatotoxicity: Clinical hepatitis and hepatic decompensation, including some fatalities, have been reported. Extra ...

APTIVUS Competitive Set

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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.

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Clinical Trial Registry

2 trials
Trial Sponsor ID Phase Status Title
NCT00537394 results posted A5241 10395, ACTG A5241 Ph 3 completed Optimizing Treatment for Treatment-Experienced, HIV-Infected People
NCT02244190 1182.124 Ph 1 completed Bioequivalence of Two Different Oral Solutions Tipranavir Administered in Combination With Ritonavir to Healthy Volunteers
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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.

APTIVUS FDA Label Details

Indications & Usage

FDA Label (PDF)

APTIVUS is indicated for the treatment of HIV-1 Infection.

⚠️ BOXED WARNING

WARNING: HEPATOTOXICITY and INTRACRANIAL HEMORRHAGE WARNING: HEPATOTOXICITY and INTRACRANIAL HEMORRHAGE See full prescribing information for complete boxed warning. Clinical hepatitis and hepatic decompensation including some fatalities. Extra vigilance is warranted in patients with chronic hepatiti...

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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