Raltegravir
Raltegravir is a pharmaceutical drug with 132 clinical trials. Historical success rate of 91.5%.
Success Metrics
Based on 108 completed trials
Phase Distribution
Phase Distribution
30
Early Stage
16
Mid Stage
54
Late Stage
Highest Phase Reached
Phase 4Trial Status & Enrollment
90.0%
108 of 120 finished
10.0%
12 ended early
0
trials recruiting
132
all time
Detailed Status
Development Timeline
Analytics
Development Status
Trials by Phase
Trials by Status
Recent Activity
Renal Transplantation and Raltegravir in HIV-Infected Patients
A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Following Virological Failure of a Standard Non-nucleoside Reverse Transcriptase Inhibitor (NNRTI)+2N(t)RTI First Line Regimen
Pharmacokinetic Study of Antiretroviral Drugs and Related Drugs During and After Pregnancy
Population Pharmacokinetics of Antiretroviral in Children
Simplification Study of HIV-1 Infected Patients With Virological Suppression Under the Combination of Lamivudine (150 mg BID) Plus Raltegravir (400 mg BID) Switching to Lamivudine (300 mg QD) Plus Raltegravir (1200 mg QD) : Roll-over Study of the RALAM
Clinical Trials (132)
Renal Transplantation and Raltegravir in HIV-Infected Patients
A Trial of 2 Options for Second Line Combination Antiretroviral Therapy Following Virological Failure of a Standard Non-nucleoside Reverse Transcriptase Inhibitor (NNRTI)+2N(t)RTI First Line Regimen
Pharmacokinetic Study of Antiretroviral Drugs and Related Drugs During and After Pregnancy
Population Pharmacokinetics of Antiretroviral in Children
Simplification Study of HIV-1 Infected Patients With Virological Suppression Under the Combination of Lamivudine (150 mg BID) Plus Raltegravir (400 mg BID) Switching to Lamivudine (300 mg QD) Plus Raltegravir (1200 mg QD) : Roll-over Study of the RALAM
Bone and Body Comp: A Sub Study of the SECOND-LINE Study
Clinical Trial to Evaluate the Effect of Raltegravir Intensification (1.200 mg QD) on the Gut Microbiota of Chronically HIV-1 Infected Subject Over Time: THE RAGTIME STUDY
Study With Dual Therapy Including Lamivudine (300 mg QD) Plus Raltegravir (1200 mg QD) in Virologically Suppressed HIV-1 Infected Patients Experiencing Inconvenience, Toxicity, Negative Impact on Co-morbidities or Risk of Drug-drug Interactions With Their Current Regimen
Antiretroviral Regimens Containing Raltegravir for Prophylaxis of Mother-to-child-transmission of HIV Infection
Combination Antiretroviral Therapy (cART) for PBC
Research In Viral Eradication of HIV Reservoirs
Raltegravir for HAM/TSP
Pregnancy and Neonatal Outcomes Following Antenatal Exposure to Raltegravir: a Pooled Analysis From the European Pregnancy and Paediatric Infections Cohort Collaboration (EPPICC)
A Study of GSK1349572 Versus Raltegravir (RAL) With Investigator Selected Background Regimen in Antiretroviral-Experienced, Integrase Inhibitor-Naive Adults
Evaluating the Safety and Pharmacokinetics of Raltegravir in Infants
Safety, Tolerance and Pharmacokinetics of Raltegravir-Containing Antiretroviral Therapy in Infants, Children Infected With HIV and TB
Safety and Pharmacokinetics of Raltegravir in HIV-1-Exposed Newborn Infants at Risk of Acquiring HIV-1 Infection
Optimizing Treatment for Treatment-Experienced, HIV-Infected People
Study of Viral Load Decay Rates in HIV Infected Participants Starting Treatment With Raltegravir (RAL) and Emtricitabine/Tenofovir Disoproxil Fumarate (TDF)
Effect on Liver Fat and Metabolic Parameters When Switching a Protease Inhibitor or Efavirenz to Raltegravir
Drug Details
- Intervention Type
- DRUG
- Total Trials
- 132