Key Insights

Highlights

Success Rate

89% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

9.1%

1 terminated out of 11 trials

Success Rate

88.9%

+2.4% vs benchmark

Late-Stage Pipeline

55%

6 trials in Phase 3/4

Results Transparency

38%

3 of 8 completed with results

Key Signals

3 with results89% success

Data Visualizations

Phase Distribution

10Total
P 2 (4)
P 3 (6)

Trial Status

Completed8
Unknown2
Terminated1

Trial Success Rate

88.9%

Benchmark: 86.5%

Based on 8 completed trials

Clinical Trials (11)

Showing 11 of 11 trials
NCT03563742Phase 3TerminatedPrimary

A Study to Determine the Safety and Efficacy of Rilpivirine in Treatment-naive Indian Participants With Human Immunodeficiency Virus Type 1 (HIV-1) Infection

NCT02452242Phase 2CompletedPrimary

Safety, PK and PD Study of ABX464 in Untreated HIV Patients

NCT00294918Phase 2Completed

An Efficacy and Safety Trial of Serostim® in the Maintenance of the Treatment Effect Obtained During the Study of Serostim® in Human Immunodeficiency Virus-associated Adipose Redistribution Syndrome

NCT00294164Phase 2Completed

Safety and Efficacy Trial of Serostim® in the Treatment of Subjects With Human Immunodeficiency Virus-associated Adipose Redistribution Syndrome (HARS)

NCT00727597Phase 3CompletedPrimary

A Study in Underrepresented Patient Population or Regimen Tolerability: SUPPoRT

NCT00749840CompletedPrimary

Attitudes and Beliefs and the Steps of HIV Care

NCT00888446Phase 2CompletedPrimary

Safety and Immunogenicity Study of tgAAC09, an HIV Vaccine in an Adeno-associated Virus (AAV) Capsid

NCT00262522Phase 3CompletedPrimary

Study of Lopinavir/Ritonavir Tablets Versus Soft Gel Capsules and Once Daily Versus Twice Daily Administration, When Coadministered With Nucleoside Reverse Transcriptase Inhibitors in Antiretroviral Naive Human Immunodeficiency Virus Type 1 Infected Subjects

NCT00358917Phase 3CompletedPrimary

Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Administration When Coadministered With Nucleoside/Nucleotide Reverse Transcriptase Inhibitors in Antiretroviral-Experienced Human Immunodeficiency Virus Type 1 Infected Subjects

NCT00332306Phase 3Unknown

Safety and Efficacy of Two Once Daily Anti Retroviral Treatment Regimens Along With Anti-tuberculosis Treatment

NCT00376012Phase 3Unknown

Short Course Intermittent Regimens for the Treatment of HIV-Associated Tuberculosis

Showing all 11 trials

Research Network

Activity Timeline