Key Insights

Highlights

Success Rate

100% trial completion (above average)

Published Results

11 trials with published results (6%)

Research Maturity

139 completed trials (81% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

0.0%

0 terminated out of 171 trials

Success Rate

100.0%

+13.4% vs benchmark

Late-Stage Pipeline

2%

3 trials in Phase 3/4

Results Transparency

8%

11 of 139 completed with results

Key Signals

11 with results100% success

Data Visualizations

Phase Distribution

171Total
Not Applicable (11)
Early P 1 (3)
P 1 (154)
P 3 (1)
P 4 (2)

Trial Status

Completed139
Unknown26
Recruiting2
Withdrawn2
Not Yet Recruiting2

Trial Success Rate

100.0%

Benchmark: 86.6%

Based on 139 completed trials

Clinical Trials (171)

Showing 20 of 20 trials
NCT07345130Phase 1CompletedPrimary

A Bioequivalence Study of Advil Tablet (Mini) (Ibuprofen 200 mg) Versus Advil Tablet (Ibuprofen 200 mg) in Healthy Adult Subjects Under Fasted Conditions and Bioavailability Assessment of Advil Tablet (Mini) Under Fed Conditions

NCT07813468Phase 1Recruiting

A Randomized, Double-Blind, Positive-Controlled, Parallel Pharmacokinetic Phase I Clinical Study of Cetuximab Injection Versus Erbitux in Healthy Male Subjects

NCT07769359Phase 1CompletedPrimary

Bioequivalence and Adhesion of a Rotigotine Patch in Healthy Subjects

NCT07763912Not ApplicableCompletedPrimary

Clinical Study to Determine Bioequivalence Between Two Oral Medications of Sitagliptin/Metformin in Prolonged-release Tablets With 50 mg/1000 mg in Healthy Subjects, Fed Study.

NCT07698288Not ApplicableCompletedPrimary

Clinical Study to Determine Bioequivalence of Oral Tamsulosin Products as 0.4 mg Prolonged-release Tablets in Male Subjects Under Fed Conditions

NCT06987773Phase 1CompletedPrimary

Study on Sapropterin Dihydrochloride Oral Suspension in Healthy Subjects Under Fed Conditions

NCT07393022Phase 1Completed

Bioequivalence Study of Levetiracetam 1500 mg Coated Granules in Healthy, Male Subjects

NCT03340753Phase 1CompletedPrimary

Bioavailability of KBP-5074 Tablet vs Capsule Formulations

NCT07096869Phase 1RecruitingPrimary

Bioequivalence Study of Paclitaxel Protein-bound Particles for Injectable Suspension (Albumin-bound) in Breast Cancer Patients

NCT06655194Phase 1CompletedPrimary

A Study to Learn if There is a Difference in the Blood Levels of Acetylsalicylic Acid When Taken as Different Chewable Tablets on an Empty Stomach by Healthy Participants

NCT06830954Phase 1Not Yet RecruitingPrimary

Bioequivalence Study of Fluvastatin Sodium Extended Release Tablets in Healthy Participants

NCT02206295Phase 1CompletedPrimary

Study in Healthy Male Subjects to Demonstrate Bioequivalence of 1600 μg Selexipag Administered as Eight Tablets of 200 μg or as Single Tablet of 1600 μg

NCT06778304Phase 1CompletedPrimary

Bioequivalence Clinical Trial of Recombinant Human Follicle-stimulating Hormone JZB30

NCT06758531Not ApplicableNot Yet Recruiting

Coffee Bioequivalence Trial

NCT05014490Phase 1CompletedPrimary

Bioequivalence Study of Test and Reference 120 mg Etoricoxib Film-coated Tablets in Healthy Volunteers

NCT06563856Phase 1Completed

A Study of TEPEZZA Subcutaneous Administration in Healthy Adults

NCT06331715Phase 4CompletedPrimary

Bioequivalence Study of Palbociclib 125 mg Capsules of Iclos vs. Ibrance (Palbociclib) Capsules 125 mg

NCT04268472Not ApplicableCompletedPrimary

Bioequivalence Study of GP30101 800 mg (GEROPHARM) Versus PREZISTA® 800 mg ("Jonson&Jonson", Russia)

NCT06497049Phase 1Completed

Open Randomized Study of Comparative Pharmacokinetics and Biosimilarity of GP40221 (GEROPHARM LLC, Russia) and Ozempic®.

NCT05883124Phase 1CompletedPrimary

Rivastigmine Bioequivalence Trial With Multiple Applications of Transdermal Patches (9.5 mg/24 h)

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