Key Insights

Highlights

Success Rate

94% trial completion (above average)

Published Results

37 trials with published results (32%)

Research Maturity

103 completed trials (89% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

6.0%

7 terminated out of 116 trials

Success Rate

93.6%

+7.1% vs benchmark

Late-Stage Pipeline

16%

19 trials in Phase 3/4

Results Transparency

36%

37 of 103 completed with results

Key Signals

37 with results94% success

Data Visualizations

Phase Distribution

107Total
Not Applicable (2)
P 1 (70)
P 2 (16)
P 3 (14)
P 4 (5)

Trial Status

Completed103
Terminated7
Unknown3
Withdrawn1
Recruiting1
Active Not Recruiting1

Trial Success Rate

93.6%

Benchmark: 86.5%

Based on 103 completed trials

Clinical Trials (116)

Showing 20 of 20 trials
NCT02951052Phase 3Active Not RecruitingPrimary

Study Evaluating the Efficacy, Safety, and Tolerability of Switching to Long-acting Cabotegravir Plus Long-acting Rilpivirine From Current Antiretroviral Regimen in Virologically Suppressed HIV-1-infected Adults

NCT06719310Phase 1RecruitingPrimary

Phase Ib/IIa Clinical Study of ACC017 Tablets

NCT02120352Phase 2CompletedPrimary

A Phase IIb Study to Evaluate a Long-Acting Intramuscular Regimen for Maintenance of Virologic Suppression (Following Induction With an Oral Regimen of GSK1265744 and Abacavir/Lamivudine) in Human Immunodeficiency Virus Type 1 (HIV-1) Infected, Antiretroviral Therapy-Naive Adult Subjects

NCT01910402Phase 3CompletedPrimary

A Study to Determine Safety and Efficacy of Dolutegravir/Abacavir/Lamivudine (DTG/ABC/3TC) in Human Immunodeficiency Virus (HIV)-1 Infected Antiretroviral Therapy (ART) Naïve Women (ARIA)

NCT02831764Phase 3CompletedPrimary

An Efficacy, Safety, and Tolerability Study Comparing Dolutegravir (DTG) Plus Lamivudine (3TC) With Dolutegravir Plus Tenofovir/Emtricitabine in Treatment naïve HIV Infected Participants (Gemini 2)

NCT00071760Phase 2CompletedPrimary

Study Of An Investigational Regimen Including FDA Approved HIV Drugs In HIV-Infected Pediatric Subjects

NCT02831673Phase 3CompletedPrimary

An Efficacy, Safety, and Tolerability Study Comparing Dolutegravir Plus Lamivudine With Dolutegravir Plus Tenofovir/Emtricitabine in Treatment naïve HIV Infected Subjects (Gemini 1)

NCT02075593Phase 3CompletedPrimary

ING200336, Pharmacokinetic and Safety Study in Pregnant Women With Human Immuno Virus Infection

NCT01231516Phase 3CompletedPrimary

A Study of GSK1349572 Versus Raltegravir (RAL) With Investigator Selected Background Regimen in Antiretroviral-Experienced, Integrase Inhibitor-Naive Adults

NCT03231943Phase 1CompletedPrimary

GSK3640254 First Time in Human (FTIH) Study in Healthy Volunteers

NCT03462810UnknownPrimary

GSK1265744 (Cabotegravir, CAB) for Named Patient/Compassionate Use in HIV

NCT02178592Phase 3CompletedPrimary

Open-label Study of Dolutegravir (DTG) or Efavirenz (EFV) for Human Immunodeficiency Virus (HIV) - Tuberculosis (TB) Co-infection

NCT03234036Phase 1CompletedPrimary

A Two-part Study to Compare a Tablet and Capsule Formulation of GSK2838232 With and Without Food, and to Assess the Safety and Drug Levels of Repeated Once-daily Doses of GSK2838232 Without Ritonavir

NCT03368053Phase 1CompletedPrimary

Long-term Immunogenicity of the HIV gp120-NefTat/AS01B Vaccine (GSK SB732461)

NCT01536873Not ApplicableCompletedPrimary

Dolutegravir Expanded Access Study

NCT03149848Phase 1CompletedPrimary

Effect of Rifabutin on the Pharmacokinetics of Oral Cabotegravir in Healthy Subjects

NCT02354937Phase 1CompletedPrimary

Pharmacokinetics Study of GSK1265744 in Subjects With Severe Renal Impairment

NCT02478463Phase 1CompletedPrimary

Pharmacokinetic Study of Cabotegravir Long-acting in Healthy Adult Volunteers

NCT01031472Phase 1CompletedPrimary

A Study to Assess Relative Bioavailability and Food Effect of New Formulations of GSK2248761

NCT03310515CompletedPrimary

Incidence of Human Immunodeficiency Virus-1 (HIV-1) Infection in HIV-1 Uninfected High Risk Men Who Have Sex With Men

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