Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

11.6%

141 terminated/withdrawn out of 1220 trials

Success Rate

83.0%

-3.5% vs industry average

Late-Stage Pipeline

28%

341 trials in Phase 3/4

Results Transparency

57%

395 of 690 completed trials have results

Key Signals

173 recruiting395 with results108 terminated33 withdrawn

Enrollment Performance

Analytics

Phase 1
330(34.7%)
Phase 3
276(29.1%)
Phase 2
252(26.5%)
Phase 4
65(6.8%)
N/A
24(2.5%)
Early Phase 1
3(0.3%)
950Total
Phase 1(330)
Phase 3(276)
Phase 2(252)
Phase 4(65)
+2 more

Activity Timeline

Global Presence

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Clinical Trials (1220)

Showing 20 of 1220 trials
NCT07387471Phase 2Active Not Recruiting

Study to Assess Change in Disease Activity of Oral Venetoclax in Adult Participants With Recurring Relapsed or Refractory (R/R) Waldenström Macroglobulinemia (WM)/Lymphoplasmacytic Lymphoma (LPL)

Role: lead

NCT07306832Phase 1Recruiting

A Study to Assess Adverse Events and How Intravenous (IV) Pivekimab Sunirine Moves Through the Body in Pediatric Participants With Relapsed or Refractory Acute Myeloid Leukemia (AML)

Role: lead

NCT07539844Recruiting

Study to Assess Prevalence of the Folate Receptor Alpha (FRa) in Adult Female Participants With Ovarian Cancer in Intercontinental (InterCon) Countries

Role: lead

NCT06772623Phase 1Recruiting

Study to Evaluate Adverse Events and Efficacy of Intravenous (IV) Telisotuzumab Adizutecan in Combination With a PD-1 Immune Checkpoint Inhibitor in Adult Participants With Advanced or Metastatic Non-Squamous NSCLC With No Prior Treatment for Advanced Disease, and No Actionable Genomic Alterations

Role: lead

NCT07226791Phase 2Recruiting

Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity in Adult Participants Undergoing Open Abdominal Ventral Hernia Repair

Role: lead

NCT05889182Phase 3Recruiting

A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib in Adult and Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-TNF Therapy

Role: lead

NCT07284342Recruiting

A Study to Assess Change in Sleep Disturbances of Adult Participants With Advanced Parkinson's Disease Receiving Subcutaneous Foslevodopa/Foscarbidopa

Role: lead

NCT06012240Phase 3Recruiting

A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adult and Adolescent Participants With Severe Alopecia Areata

Role: lead

NCT07738887Phase 2Not Yet Recruiting

Epcoritamab Plus Venetoclax Plus Ibrutinib in Patients With Chronic Lymphocytic Leukemia With TP53 Alterations

Role: collaborator

NCT07071519Phase 3Recruiting

A Study to Learn More About How Risankizumab Works in Young Participants With Ulcerative Colitis

Role: lead

NCT06100744Phase 3Recruiting

A Study to Assess Adverse Events, Change in Disease Activity, and How the Drug Moves Through the Body in Children With Juvenile Psoriatic Arthritis (jPsA) Receiving Subcutaneously Injected Risankizumab or Adalimumab

Role: lead

NCT07581002Phase 2Recruiting

A Study to Assess Adverse Events and Change in Disease Activity When Intravenous (IV) Pivekimab Sunirine is Given in Combination With Oral Venetoclax and IV or Subcutaneous Azacitidine in Adult Participants With Acute Myeloid Leukemia (AML)

Role: lead

NCT07197307Phase 2Recruiting

Combining Loncastuximab Tesirine and Epcoritamab in Relapsed/Refractory Diffuse Large B-cell Lymphoma (DLBCL)

Role: collaborator

NCT07023302Phase 3Active Not Recruiting

A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adult and Adolescent Participants in Japan With Alopecia Areata

Role: lead

NCT06575192Phase 3Recruiting

Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matrix Breast Reconstruction (ADORA) in Adult Participants

Role: lead

NCT07502417Phase 1Completed

A Phase 1 Study to Assess the Effect of ABBV-722 on Ethinyl Estradiol and Levonorgestrel Drug Levels in Healthy Adult Female Participants

Role: lead

NCT06806293Phase 3Active Not Recruiting

Study of Oral Atogepant to Assess Adverse Events and Change in Disease Activity in Adult Participants With Menstrual Migraine

Role: lead

NCT05125302Phase 3Recruiting

Study to Assess Adverse Events and Disease Activity of Oral Ubrogepant Tablets for the Acute Treatment of Migraine in Children and Adolescents (Ages 6-17)

Role: lead

NCT03848143Phase 2Completed

Intraoral Administration of Botox in Patients With Dentoalveolar Neuropathic Pain

Role: collaborator

NCT06712628Recruiting

A Comparison Study of Persistence of UPadacitinib vs. TNF-inhibitoRs In a German Real-world SettING

Role: lead