Drug & intervention

tipranavir

RxCUI 190548

Clinical trials18
Recruiting0
Related conditions4
Synonyms5

Understanding this RxNorm record

RxNorm identifiers distinguish ingredients, specific strengths, dose forms, and branded products. They help connect equivalent terminology across data sources; an RxNorm entry does not by itself establish that a product is currently marketed, approved for a particular use, or appropriate for an individual.

Clinical-trial associations reflect registry-reported intervention names and verified mappings where available. A medication listed in a trial may be investigational for that condition. Consult the original study record and official prescribing information for indications and safety details.

Terminology source: National Library of Medicine RxNorm. Trial source: ClinicalTrials.gov.

RxNorm ingredient and formulation relationships

Source-verified product relationships. Every strength, delivery form and RxCUI remains a separate clinical concept.

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Background context

Tipranavir

Tipranavir (TPV) is a nonpeptidic HIV-1 protease inhibitor manufactured by Boehringer Ingelheim under the trade name Aptivus. It is used as part of combination antiretroviral therapy for treatment-experienced patients with HIV-1 infection whose virus is resistant to more than one protease inhibitor. It is not approved for treatment-naïve patients. Tipranavir can retain activity against some HIV-1 strains resistant to other protease inhibitors and is indicated for patients who are resistant to other treatments. Resistance to tipranavir itself seems to require multiple protease mutations. The U.S. Food and Drug Administration (FDA) granted accelerated approval to tipranavir capsules on June 22, 2005. Pediatric use and the oral solution formulation were approved on June 24, 2008, for treatment-experienced pediatric and adolescent patients. Tipranavir is administered only with ritonavir as a pharmacokinetic enhancer and in combination with other antiretroviral drugs. It is effective in salvage therapy for patients with drug resistance, but its current clinical role is limited by toxicity concerns. Side effects of tipranavir may be more severe than those of other antiretrovirals. Some side effects include intracranial hemorrhage, hepatitis, hepatic decompensation, hyperglycemia and diabetes mellitus. The drug has also been shown to cause increases in total cholesterol and triglycerides. Aptivus labeling has a black box warning regarding hepatotoxicity and intracranial hemorrhage. Tipranavir is currently rarely used, mainly because of intolerance, hepatotoxicity, the need for...

Background only. Canonical identity remains RxNorm; clinical-trial relationships come from ClinicalTrials.gov.

Clinical trials

18 shown
A Post Marketing Surveillance Study Assessing the Long-term Efficacy and Safety of Aptivus Co-administered With Low-dose Ritonavir in Treatment Experienced Patients With HIV-1 Infection in the Daily Clinical Practice.NCT00976950 · 2009-09-01
COMPLETED
Surveillance Cohort Long-term Toxicity Antiretrovirals in HIV-infected Patients Enrolled in TPV CohortNCT00805857 · 2008-06-01
WITHDRAWN
Optimizing Treatment for Treatment-Experienced, HIV-Infected PeopleNCT00537394 · 2008-01-01
COMPLETED
Tipranavir/Ritonavir Low Dose Pharmacokinetics in Treatment Naive PatientsNCT00530920 · 2007-10-01
COMPLETED
Comparison of TPV/r to DRV/r in Triple Class Experienced Patient With Resistance to > 1 PINCT00517192 · 2007-09-01
TERMINATED
Pharmaco-epidemiological Description of the Population Treated With Aptivus Under Market Conditions, Safety & EfficacyNCT00615290 · 2007-06-01
COMPLETED
Safety and Antiviral Activity of TPV in HCV and/or HBV HIV Coinfected Patients TDM Randomised Pilot EvaluationNCT00447902 · 2007-03-01
TERMINATED
SPRING: Safety, Efficacy, Pharmacokinetics of tipRanavir/r IN Race/Gender HIV+ Patients Randomized to TDM or SoCNCT00440271 · 2007-02-01
TERMINATED
Observational Non-interventional Study (Anwendungsbeobachtung) With Aptivus® (Tipranavir) in HIV-infected Patients.NCT00531206 · 2006-08-01
COMPLETED
Pharmacokinetics (PK) of Tipranavir/Ritonavir, Ribavirin, Pegylated Interferon (Peg INF) in Hepatitis C (HCV) Subjects With Mild Hepatic Impairment and in HCV, Hepatitis B (HBV), Hepatitis D Infected Subjects or Alcoholic Cirrhosis With Moderate Hepatic ImpairmentNCT02259855 · 2006-01-01
COMPLETED
Tipranavir Expanded Access Program (EAP) in PI-experienced Patients With HIV-1 InfectionNCT00097799 · 2004-12-01
APPROVED_FOR_MARKETING
An Open Label Safety Study of Tipranavir Co-administered With Low-dose Ritonavir in Patients With Advanced HIV-1 Infection and Limited Treatment Options.NCT00933205 · 2004-05-01
APPROVED_FOR_MARKETING
Tipranavir in Patients With Progressive, Systemic HIV-1 Disease Who Have Failed or Are Intolerant to Currently Approved Treatments for HIV InfectionNCT00062660 · 2003-05-01
APPROVED_FOR_MARKETING
Dual Boosted - Protease Inhibitor (PI) Pharmacokinetics (PK) Trial (Tipranavir / Ritonavir) in Highly Treatment-experienced HIV-1 Infected PatientsNCT00056641 · 2003-02-18
COMPLETED
HIV Infection And Metabolic Abnormalities Protocol 1 (HAMA001)NCT00192660 · 2003-02-01
COMPLETED
Randomized Evaluation of Strategic Intervention in Multidrug Resistant Patients With Tipranavir (RESIST)NCT00054717 · 2003-01-01
COMPLETED
3 TPV/RTV Doses in Multiple ARV Experienced Patients - Tipranavir Dose Defining StudyNCT00275444 · 2002-03-29
COMPLETED
Rollover Trial Safety and Tolerability of Combination Tipranavir and Ritonavir Use in HIV 1 Infected SubjectsNCT00146328 · 2001-04-01
COMPLETED

Drug identity and terminology: RxNorm. Trial relationships: ClinicalTrials.gov.