RITONAVIR

Post-LOESM

ritonavir

Hetero

ANDAORALTABLET

Approved

Sep 2018

Lifecycle

Post-LOE

Competitive Pressure

30/100

Clinical Trials

Data completeness

5/8 — Partial

RITONAVIR (ritonavir) by Hetero is hiv protease inhibitors [moa]. Approved for combination with other antiretroviral agents for the treatment of hiv-1 infection ( ). First approved in 2018.

Drug data last refreshed 6h ago

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Mechanism of Action

HIV Protease Inhibitors

Pharmacologic Class:

Cytochrome P450 3A Inhibitor

Indications (1)

combination with other antiretroviral agents for the treatment of HIV-1 infection ( )

Clinical Trials (20)

NCT00084058Phase 1/2Completed

Safety of Saquinavir and High Doses of Lopinavir/Ritonavir in Children With HIV

26 enrolled

HIV Infections

NCT00001075N/ACompleted

The Effectiveness of Ritonavir Plus Zidovudine Plus Lamivudine in HIV-Infected Patients

55 enrolled

HIV Infections

NCT00000920Phase 1Completed

Fortovase (Saquinavir) Given With Low-Dose Ritonavir, Zidovudine, and Lamivudine to HIV-Positive Pregnant Women During and After Pregnancy and to Their Newborns

24 enrolled

HIV InfectionsPregnancy

NCT00001133Phase 1Completed

Safety and Tolerance of Indinavir Plus Ritonavir in HIV-Positive Patients Failing Therapy With Amprenavir, Nelfinavir, or Saquinavir

50 enrolled

HIV Infections

NCT00046033Phase 2Completed

Comparing Standard-Dose Versus Adjusted-Dose Lopinavir/Ritonavir Therapy in HIV-Infected Persons With Drug Resistance

118 enrolled

HIV Infections

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Data Sources

Drug label: DailyMed / FDA
Clinical trials: ClinicalTrials.gov
Patent data: FDA Orange Book
Spending data: CMS Medicare

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.