Key Insights

Highlights

Success Rate

80% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 39/100

Termination Rate

19.0%

4 terminated out of 21 trials

Success Rate

80.0%

-6.5% vs benchmark

Late-Stage Pipeline

52%

11 trials in Phase 3/4

Results Transparency

44%

7 of 16 completed with results

Key Signals

7 with results80% success

Data Visualizations

Phase Distribution

18Total
P 1 (2)
P 2 (5)
P 3 (9)
P 4 (2)

Trial Status

Completed16
Terminated4
Withdrawn1

Trial Success Rate

80.0%

Benchmark: 86.5%

Based on 16 completed trials

Clinical Trials (21)

Showing 20 of 20 trials
NCT00046176Phase 3CompletedPrimary

A HIV Study Of A Fixed-Dose Combination Tablet In Antiretroviral Experienced Patients

NCT00044577Phase 3CompletedPrimary

New Tablet Containing Two FDA Approved Anti-HIV Drugs For Antiretroviral Therapy Experienced HIV-1 Infected Subjects

NCT03327740CompletedPrimary

PRJ2203: Dolutegravir Post Authorization Safety Study (PASS)

NCT00197145Phase 3TerminatedPrimary

Study Of Chemokine Coreceptor 5 (CCR5) Antagonist GW873140 In R5-Tropic Treatment-Experienced HIV-Infected Subjects

NCT01227824Phase 3CompletedPrimary

A Trial Comparing GSK1349572 50mg Once Daily to Raltegravir 400mg Twice Daily

NCT01205243CompletedPrimary

ZIAGEN® Post-marketing Surveillance

NCT00094523Phase 3CompletedPrimary

Fosamprenavir Versus Other Protease Inhibitors

NCT01263015Phase 3CompletedPrimary

A Trial Comparing GSK1349572 50mg Plus Abacavir/Lamivudine Once Daily to Atripla (Also Called The SINGLE Trial)

NCT00102778Phase 2TerminatedPrimary

GW873140 In Combination With Kaletra In HIV Infected Subjects

NCT00242840Phase 3CompletedPrimary

Observational Study Of A Protease Inhibitor (PI) Containing Regimen In Subjects With PI Mutations Selected During Prior Treatment With GW433908 (Fosamprenavir)

NCT00242879Phase 2TerminatedPrimary

A Dose Ranging Study Of GW640385 Boosted With Ritonavir (Rtv) In Comparison To A RTV-Boosted Protease Inhibitor (PI) In HIV-1 Infected PI-Experienced Adults

NCT00257621Phase 2CompletedPrimary

GW640385 Plus Ritonavir And NRTIs For 48 Weeks In HIV-1 Infected Adults

NCT00104429Phase 2TerminatedPrimary

GW873140 In Combination With Combivir In HIV Infected Subjects

NCT00082394Phase 4CompletedPrimary

A Study Comparing The Safety, Tolerability and Efficacy of Trizivir VS Combivir & Atazanavir In Subjects With HIV

NCT00089583Phase 2CompletedPrimary

48-Week Study Of GW433908 And Ritonavir Or GW433908 Alone, Twice Daily In Pediatric Patients With HIV Infection

NCT01283100Phase 1WithdrawnPrimary

A Drug Interaction Study Evaluating Plasma GSK2248761 and GSK1349572 Pharmacokinetics in Healthy Adult Subjects.

NCT00450580Phase 3CompletedPrimary

HIV-1 Infection Study of Once a Day Versus Twice a Day Protease Inhibitor in Antiretroviral Treatment Naive Adults

NCT01597648Phase 1CompletedPrimary

A Study to Evaluate the Bioequivalence of a Combined Formulated Tablet Compared With Maraviroc and Combivir™

NCT00440947Phase 3CompletedPrimary

Induction/Simplification With Atazanavir + Ritonavir + Abacavir/Lamivudine Fixed-Dose Combination In HIV-1 Infection

NCT00481390CompletedPrimary

Prospective Epidemiological Study Of The Prevalence Of HLA-B*5701 In HIV-1 Infected Patients

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