Success Metrics

Clinical Success Rate
96.7%

Based on 29 completed trials

Completion Rate
97%(29/30)
Active Trials
1(3%)
Results Posted
45%(13 trials)
Terminated
1(3%)

Phase Distribution

Ph phase_2
13
33%
Ph not_applicable
3
8%
Ph phase_1
4
10%
Ph phase_4
8
21%
Ph phase_3
8
21%

Phase Distribution

4

Early Stage

13

Mid Stage

16

Late Stage

Phase Distribution36 total trials
Phase 1Safety & dosage
4(11.1%)
Phase 2Efficacy & side effects
13(36.1%)
Phase 3Large-scale testing
8(22.2%)
Phase 4Post-market surveillance
8(22.2%)
N/ANon-phased studies
3(8.3%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

93.5%

29 of 31 finished

Non-Completion Rate

6.5%

2 ended early

Currently Active

1

trials recruiting

Total Trials

39

all time

Status Distribution
Active(1)
Completed(29)
Terminated(2)
Other(7)

Detailed Status

Completed29
unknown6
Terminated1
Active, not recruiting1
Suspended1
Withdrawn1

Development Timeline

Analytics

Development Status

Total Trials
39
Active
1
Success Rate
96.7%
Most Advanced
Phase 4

Trials by Phase

Phase 14 (11.1%)
Phase 213 (36.1%)
Phase 38 (22.2%)
Phase 48 (22.2%)
N/A3 (8.3%)

Trials by Status

terminated13%
active_not_recruiting13%
completed2974%
suspended13%
withdrawn13%
unknown615%

Recent Activity

Clinical Trials (39)

Showing 20 of 39 trialsScroll for more
NCT00115609Phase 3

Efficacy of Tenofovir-Emtricitabine and Efavirenz in HIV Infected Patients With Tuberculosis (ANRS129)

Completed
NCT05979311Phase 3

A Study to Evaluate the Efficacy, Safety, and Tolerability of Using an Oral Once-daily 2 Drug Regimen Compared to an Oral Once-daily 3 Drug Regimen for the Treatment of Human Immunodeficiency Virus (HIV)-1 in Adults Who Have Not Previously Taken Antiretroviral Therapy

Active Not Recruiting
NCT00042289

Pharmacokinetic Study of Antiretroviral Drugs and Related Drugs During and After Pregnancy

Completed
NCT04862975

Pharmacokinetics of Antiretroviral Drugs in Lactating Women and Breastmilk Fed Infants Under 6 Months of Age in Botswana

Completed
NCT01400412Phase 2

Bone, Immunologic, and Virologic Effects of a Antiretroviral Regimen

Completed
NCT00799864Phase 2

A Study to Evaluate the Pharmacokinetics, Safety, Tolerability, and Antiviral Activity of Rilpivirine (TMC278) in Human Immunodeficiency Virus Infected Adolescents and Children Aged Greater Than or Equal to 6 Years

Completed
NCT03218085

Role of Exogenous and Endogenous Sex Hormones on Tenofovir and Emtricitabine Disposition in Female Genital Tract

Completed
NCT00380159Phase 2

Open-Label, 48-Week Extension Study of Elvucitabine in Combination With Background Antiretroviral Therapy (ART) for Participants Who Have Completed Study ACH443-014A

Completed
NCT02475915Phase 1

Efficacy of VHM After Treatment Interruption in Subjects Initiating ART During Acute HIV Infection

Completed
NCT01505114Phase 2

Evaluating the Safety and Tolerability of Antiretroviral Drug Regimens Used as Pre-Exposure Prophylaxis to Prevent HIV Infection in At-Risk Men Who Have Sex With Men and in At-Risk Women

Completed
NCT00006144Phase 2

A Study of HIV-Disease Development in Aging

Completed
NCT00102206Phase 2

A Comparison of Two Anti-HIV Drug Regimens for Youth Who Have Failed Prior Therapy

Completed
NCT00051831Not Applicable

Effect of an Enfuvirtide-based Anti-HIV Drug Regimen on Latent HIV Reservoirs in Treatment Naive Adults

Completed
NCT00036452Phase 2

A Study to Compare Anti-HIV Drugs Given Twice a Day or Once a Day, With or Without Direct Observation

Completed
NCT00087464Not Applicable

Three Month Course of Anti-HIV Medications for People Recently Infected With HIV

Withdrawn
NCT01709084Phase 3

A Clinical Trial Comparing the Efficacy of Tenofovir Disoproxil Fumarate/Emtricitabine/Rilpivirine (TDF/FTC/RPV) Versus TDF/FTC/Efavirenz (TDF/FTC/EFV) in Patients With Undetectable Plasma HIV-1 RNA on Current First-line Treatment

Completed
NCT04477096Phase 1

Evaluation of Drug Interaction Between HS-10234 and Emtriccitabine

Completed
NCT01803074Phase 2

Study to Evaluate a HIV Drug for the Treatment of HIV Infection

Completed
NCT01335620Phase 4

The Safety, Pharmacokinetic Profile and Efficacy of Raltegravir in HIV-infected Patients at Least 60 Years of Age

Completed
NCT02116660Phase 2

Evaluation of Renal Function, Efficacy, and Safety When Switching From Tenofovir/Emtricitabine Plus a Protease Inhibitor/Ritonavir, to a Combination of Raltegravir (MK-0518) Plus Nevirapine Plus Lamivudine in HIV-1 Participants With Suppressed Viremia and Impaired Renal Function (MK-0518-284)

Terminated

Drug Details

Intervention Type
DRUG
Total Trials
39