Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

0.0%

0 terminated out of 20 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

0%

0 trials in Phase 3/4

Results Transparency

7%

1 of 14 completed with results

Key Signals

1 with results100% success

Data Visualizations

Phase Distribution

20Total
P 1 (20)

Trial Status

Completed14
Recruiting3
Not Yet Recruiting1
Active Not Recruiting1
Unknown1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 14 completed trials

Clinical Trials (20)

Showing 20 of 20 trials
NCT07563894Phase 1RecruitingPrimary

Relative Bioavailability and Impact of Rabeprazole for PF-07799933, Food-Effect for PF-07799933 and PF-07799544

NCT07072234Phase 1Recruiting

Phase I Study of Allogeneic Transforming Growth Factor-beta Receptor Type 2 Knockout CD70 CAR NK Cells in Treatment Refractory Clear Cell Renal Cell Carcinoma

NCT06660420Phase 1RecruitingPrimary

Phase 1 Dose Escalation and Expansion Study of PRAME T Cell Receptor (TCR) Engineered NK Cells in Participants With Recurrent and/or Refractory Melanoma (PRAMETIME-Mel)

NCT07500298Phase 1Not Yet RecruitingPrimary

Phase 1 Study Of SAR445877 In Combination With FOLFOX6 And Bevacizumab As First-Line Treatment For Microsatellite Stable Metastatic Colorectal Cancer

NCT07413367Phase 1Active Not Recruiting

A Phase 1, Open-Label, Parallel-Group, Single-Dose Study To Compare The Pharmakokinetics Of TNX-102 SL (Cyclobenzaprine Hydrochloride Sublingual Tablet) In Non-Elderly Versus Elderly Participants

NCT03488719Phase 1CompletedPrimary

A Study to Examine the Effect of Tesofensine and Metoprolol on the 24-hour Mean Heart Rate

NCT06214858Phase 1UnknownPrimary

The Safety, Tolerability, Pharmacokinetics and Food Effects of SHEN211 Tablet in Healthy Subjects

NCT05068947Phase 1CompletedPrimary

Safety, Tolerability, and Pharmacokinetic Study of Single Ascending Dose of GV101 in Healthy Subjects

NCT03740217Phase 1CompletedPrimary

Comparison of the Relative Oral Bioavailability of GKT137831 Formulated in Capsules or in Tablets

NCT04327089Phase 1CompletedPrimary

Study to Evaluate the Pharmacokinetics and Drug-Drug Interactions of Setanaxib in Healthy Adult Male and Female Subjects

NCT03983876Phase 1CompletedPrimary

PK, Safety and Tolerability Study of AVT02 (Adalimumab) Pre-filled Syringe (PFS) vs, AVT02 Autoinjector (AI)

NCT04014257Phase 1CompletedPrimary

A Phase 1 Study of NOV1601(CHC2014) in Adult Subjects With Solid Organ Malignancies

NCT03647670Phase 1CompletedPrimary

A Study to Determine the Effects of PF-04965842 on Midazolam PK in Healthy Volunteers

NCT03883620Phase 1CompletedPrimary

Safety Study of Dengushield in Healthy Adults

NCT01091532Phase 1CompletedPrimary

A Study In Healthy People Of Multiple Doses Of UK-396,082 Given By Mouth, To Investigate The Safety, Toleration And Time Course Of Blood Concentration Of UK-396,082 And Its Effects.

NCT03273088Phase 1CompletedPrimary

Pharmacokinetic, Safety and Tolerability Study of Altebrel in Healthy Male Subjects

NCT03273192Phase 1Completed

A Study Of CinnoRA (Adalimumab-CinnaGen) And Adalimumab (Humira) In Healthy Subjects

NCT02634489Phase 1CompletedPrimary

EC905 Pharmacokinetic Profile Study

NCT02010944Phase 1CompletedPrimary

A Study to Compare How Much Solifenacin Succinate and Mirabegron Reach the Blood When Administered Together as Fixed-dose Combination Tablets and With Single Individual Tablets of the Same Medications at Three Dose Levels

NCT01415102Phase 1CompletedPrimary

A First In Human Study In Healthy People To Evaluate Safety, Toleration And Time Course Of Plasma Concentration Of Single Inhaled Doses Of PF-05212372.

Showing all 20 trials

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