Key Insights

Highlights

Success Rate

91% trial completion (above average)

Published Results

106 trials with published results (49%)

Research Maturity

168 completed trials (78% of total)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 17/100

Termination Rate

7.9%

17 terminated out of 215 trials

Success Rate

90.8%

+4.3% vs benchmark

Late-Stage Pipeline

32%

69 trials in Phase 3/4

Results Transparency

63%

106 of 168 completed with results

Key Signals

106 with results91% success17 terminated

Data Visualizations

Phase Distribution

194Total
Not Applicable (14)
Early P 1 (2)
P 1 (43)
P 2 (66)
P 3 (48)
P 4 (21)

Trial Status

Completed168
Terminated17
Unknown10
Active Not Recruiting9
Withdrawn6
Not Yet Recruiting3

Trial Success Rate

90.8%

Benchmark: 86.5%

Based on 168 completed trials

Clinical Trials (215)

Showing 20 of 20 trials
NCT06660498Phase 1Active Not RecruitingPrimary

Pomalidomide as an Immune-enhancing Agent for the Control of HIV

NCT07569913Not ApplicableNot Yet RecruitingPrimary

A Study to Evaluate the Performance, and Usability of TruPlex HIV/HepB/Syphilis Rapid Test

NCT05729568Phase 2Active Not RecruitingPrimary

A Study of Teropavimab and Zinlirvimab in Combination With Capsid Inhibitor Lenacapavir in Virologically Suppressed Adults With HIV-1 Infection

NCT02906137Not ApplicableCompletedPrimary

Gut-Associated Lymphocyte Trafficking

NCT04133012Not ApplicableCompletedPrimary

Cartography of Virologic Reservoir Related to Antiretroviral Concentrations in HIV-1 Chronic Patients Treated by a First Line Treatment Containing Dolutegravir and Associated Nucleoside / Nucleotide Reverse Transcriptase Inhibitors Backbone

NCT01453192Phase 3CompletedPrimary

Renal Transplantation and Raltegravir in HIV-Infected Patients

NCT02881320Phase 2Active Not RecruitingPrimary

Study of Bictegravir/Emtricitabine/Tenofovir Alafenamide Fixed Dose Combination in Adolescents and Children With Human Immunodeficiency Virus-1

NCT05052996Phase 2Active Not RecruitingPrimary

Study Evaluating the Safety and Efficacy of Islatravir in Combination With Lenacapavir in Virologically Suppressed People With HIV

NCT04233879Phase 3CompletedPrimary

Study of Doravirine/Islatravir (DOR/ISL 100 mg/0.75 mg) to Evaluate the Antiretroviral Activity, Safety, and Tolerability in Treatment-Naïve Participants With Human Immunodeficiency Virus Type 1 (HIV-1) Infection (MK-8591A-020)

NCT04564547Phase 2CompletedPrimary

Dose Ranging, Switch Study of Islatravir (MK-8591) and Ulonivirine (MK-8507) Once-Weekly in Virologically-Suppressed Adults With Human Immunodeficiency Virus Type 1 (HIV-1) [MK-8591-013]

NCT06657885Phase 2WithdrawnPrimary

CAbotégravir LENacapavir DUal Long Acting

NCT07308782Phase 2RecruitingPrimary

A Phase Ⅱa Clinical Study of CL-197 Capsules

NCT04776252Phase 3Active Not RecruitingPrimary

Open-label, Follow-up of Doravirine/Islatravir (DOR/ISL 100 mg/0.75mg) for Participants With Human Immunodeficiency Virus-1 (HIV-1) Infection (MK-8591A-033)

NCT05631093Phase 3Active Not RecruitingPrimary

A Switch to Doravirine/Islatravir (DOR/ISL) in Participants With Human Immunodeficiency Virus Type 1 (HIV-1) Who Are Virologically Suppressed on Antiretroviral Therapy (ART) (MK-8591A-051)

NCT03593187Phase 1CompletedPrimary

A Study Evaluating the Safety of Cal-1 (LVsh5/C46) Drug Product in HIV-1 Infected Patient With High Risk Lymphoma

NCT05630755Phase 3Active Not RecruitingPrimary

A Switch to Doravirine/Islatravir (DOR/ISL) in Participants With Human Immunodeficiency Virus Type 1 (HIV-1) Who Are Virologically Suppressed on Bictegravir/Emtricitabine/Tenofovir Alafenamide (BIC/FTC/TAF) (MK-8591A-052)

NCT05705349Phase 3Active Not RecruitingPrimary

DOR/ISL in HIV-1 Antiretroviral Treatment-naïve Participants (MK-8591A-053)

NCT02390297Active Not RecruitingPrimary

Long Term Follow up for the Detection of Delayed Adverse Events in Cal-1 Recipients

NCT02859558Phase 2CompletedPrimary

Early ART to Limit Infection and Establishment of Reservoir

NCT01152255Phase 1TerminatedPrimary

MK6186 in HIV-1 Infected Patients (MK-6186-007 AM2)

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