Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 55/100

Failure Rate

17.2%

5 terminated/withdrawn out of 29 trials

Success Rate

82.1%

-4.4% vs industry average

Late-Stage Pipeline

69%

20 trials in Phase 3/4

Results Transparency

17%

4 of 23 completed trials have results

Key Signals

4 with results

Enrollment Performance

Analytics

Phase 4
13(50.0%)
Phase 3
7(26.9%)
Phase 1
5(19.2%)
Phase 2
1(3.8%)
26Total
Phase 4(13)
Phase 3(7)
Phase 1(5)
Phase 2(1)

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (29)

Showing 20 of 29 trials
NCT04076059Phase 3Active Not Recruiting

An Efficacy and Safety Study of Enzalutamide Plus Androgen Deprivation Therapy (ADT) Versus Placebo Plus ADT in Chinese Patients With Metastatic Hormone Sensitive Prostate Cancer (mHSPC)

Role: lead

NCT04995419Phase 2Completed

A Study to Evaluate Enfortumab Vedotin (ASG-22CE) in Chinese Participants With Locally Advanced or Metastatic Urothelial Cancer Who Previously Received Platinum-containing Chemotherapy and Programmed Cell Death Protein-1 ( PD 1) / (Programmed Death Ligand-1 (PD-L1) Inhibitor Therapy

Role: lead

NCT05152628Phase 4Completed

A Study of Modigraf® (Tacrolimus Granules) to Evaluate the Pharmacokinetics and Long-term Safety and Efficacy in De Novo Pediatric Allograft Liver and Kidney Transplantation Recipients

Role: lead

NCT05153915Phase 4Completed

A Study to Evaluate the Safety and Efficacy of a Modigraf® Based Immunosuppression Regimen in De Novo Pediatric Allograft Liver and Kidney Transplantation Recipients

Role: lead

NCT04234204Phase 3Completed

A Study to Find Out if Fezolinetant Helps Reduce Moderate to Severe Hot Flashes in Women in Asia Going Through Menopause

Role: lead

NCT04451226Phase 3Completed

A Study to Assess the Safety and Tolerability of Fezolinetant in Women Seeking Treatment for Relief of Vasomotor Symptoms (VMS) Associated With Menopause

Role: lead

NCT01982071Phase 4Terminated

A Study to Evaluate the Efficacy and Safety of Micafungin Against Invasive Candidiasis or Candidemia

Role: lead

NCT04086758Phase 1Completed

A Pharmacokinetic Study of Zolbetuximab (IMAB362) in Chinese Subjects With Locally Advanced Unresectable or Metastatic Gastric or Gastro-esophageal Junction (GEJ) Adenocarcinoma

Role: lead

NCT02646774Phase 4Terminated

Post Marketing Study to Evaluate the Efficacy and Safety of Micafungin Treatment on Invasive Aspergillosis

Role: lead

NCT04562090Phase 4Completed

A Study With Mirabegron 50 mg and 25 mg in Chinese Participants With Overactive Bladder

Role: lead

NCT04501640Phase 4Completed

A Study to Investigate the Effect of Food With Mirabegron in Healthy Chinese Participants

Role: lead

NCT02706678Phase 4Completed

Efficacy and Safety Study of the Switch From Cyclosporin to Tacrolimus in Renal Transplant Recipients

Role: lead

NCT02646800Phase 4Terminated

Post Marketing Study to Evaluate the Safety and Efficacy of Micafungin Against Fungal Infections Caused by Candida Spp or Aspergillus Spp

Role: lead

NCT02268201Phase 4Terminated

A Study to Evaluate the Efficacy and Safety in Kidney Transplant Recipients When Changed From Cyclosporine to Tacrolimus Prolonged-release Capsule or Tacrolimus Capsule

Role: lead

NCT02457221Phase 3Completed

A Study to Compare the Efficacy and Safety of Tacrolimus Capsules and Cyclophosphamide Injection in Treatment of Lupus Nephritis

Role: lead

NCT03644485Phase 4Completed

Clinical Outcome of Delayed or Standard Prograf Together With Induction Therapy Followed by Conversion to Advagraf in Donation After Cardiac (or Circulatory) Death (DCD) Kidney Transplant Recipients

Role: lead

NCT04793204Phase 1Completed

A Study to Evaluate the Pharmacokinetics and Safety of Fezolinetant in Healthy Chinese Female Subjects

Role: lead

NCT04143477Phase 1Completed

A Study to Evaluate the Pharmacokinetics and Safety of ASP015K in Healthy Chinese Subjects

Role: lead

NCT03660059Phase 3Completed

A Study to Assess Safety and Efficacy of ASP015K in Participants With Rheumatoid Arthritis (RA) Who Had an Inadequate Response or Intolerance to Methotrexate (MTX)

Role: lead

NCT02392312Completed

Observational Study to Evaluate the Safety and Efficacy of ATG-F on Kidney Transplant Recipients

Role: lead