Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 15/100

Failure Rate

10.6%

521 terminated/withdrawn out of 4916 trials

Success Rate

88.5%

+1.9% vs industry average

Late-Stage Pipeline

32%

1589 trials in Phase 3/4

Results Transparency

55%

2194 of 3996 completed trials have results

Key Signals

139 recruiting2194 with results372 terminated149 withdrawn

Enrollment Performance

Analytics

Phase 1
1387(32.1%)
Phase 2
1117(25.9%)
Phase 3
1051(24.3%)
Phase 4
538(12.5%)
N/A
209(4.8%)
Early Phase 1
16(0.4%)
4318Total
Phase 1(1387)
Phase 2(1117)
Phase 3(1051)
Phase 4(538)
+2 more

Activity Timeline

Global Presence

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Clinical Trials (4916)

Showing 20 of 4916 trials
NCT04617925Phase 2Completed

A Study of Belantamab Mafodotin in Patients With Relapsed or Refractory AL Amyloidosis

Role: collaborator

NCT06134362Phase 3Active Not Recruiting

Long-term Follow-up of Long-acting Cabotegravir (CAB LA) for PrEP (Pre-exposure Prophylaxis) in Participants at Risk of Acquiring HIV (Human Immunodeficiency Virus)

Role: collaborator

NCT06734234Phase 1Active Not Recruiting

A Study to Evaluate the Safety, Tolerability, and Effects on Blood and Urine Markers of Single Ascending Dose of GSK4771261 in Healthy Participants and Participants With Autosomal Dominant Polycystic Kidney Disease

Role: lead

NCT06573281Phase 1Completed

A Study on the Safety and Immune Response to an mRNA-based RSV Investigational Vaccine in Healthy Adults Aged 18-45 Years

Role: lead

NCT07092865Phase 2Active Not Recruiting

A Study Evaluating Persistence of the Immune Response of the Adjuvanted Respiratory Syncytial Virus (RSV) Vaccine and the Safety and Immune Response Following Revaccination in Adults 18 Years of Age and Above Who Received Lung or Kidney Transplant

Role: lead

NCT02938520Phase 3Active Not Recruiting

Study to Evaluate the Efficacy, Safety, and Tolerability of Long-acting Intramuscular Cabotegravir and Rilpivirine for Maintenance of Virologic Suppression Following Switch From an Integrase Inhibitor in HIV-1 Infected Therapy Naive Participants

Role: collaborator

NCT07406334Phase 1Recruiting

A Trial to Evaluate the Safety and Reactogenicity of an Investigational Pneumococcal Vaccine in Toddlers 12 to 15 Months of Age Receiving a Single Booster Dose

Role: lead

NCT07712393Phase 1Recruiting

A Comparative Study to Investigate the Difference in Blood Levels of Two Different Formulations of GSK5784283

Role: lead

NCT07099898Phase 3Recruiting

A Study of GSK5764227 in Participants With Relapsed Small Cell Lung Cancer (SCLC)

Role: lead

NCT05334368Phase 3Recruiting

Depemokimab in Participants With Hypereosinophilic Syndrome, Efficacy, and Safety Trial

Role: lead

NCT06534892Phase 3Active Not Recruiting

An Extension and Crossover Vaccination Study on the Immune Response and Safety of a Vaccine Against Respiratory Syncytial Virus Given to Adults 60 Years of Age and Above Who Participated in RSV OA=ADJ-006 Study

Role: lead

NCT07596199Phase 3Recruiting

A Study on the Immune Response and Safety of a Combined Vaccine Against Diphtheria, Tetanus and Acellular Pertussis (dTpa) in Japanese Healthy Pregnant Women

Role: lead

NCT04494412Phase 2Completed

An Intravenous (IV) Zanamivir Pharmacokinetics (PK) Study in Hospitalized Neonates and Infants With Influenza Infection

Role: lead

NCT07177339Phase 3Recruiting

eValuating the Efficacy and Safety of InitiatinG depemokImab earLy therApy iN Chronic Obstructive Pulmonary Disorder (COPD) With Type 2 Inflammation

Role: lead

NCT07663032Phase 1Recruiting

A Study to Evaluate the Safety, Reactogenicity, and Immune Response of the GSK Vaccines Institute for Global Health (GVGH) Quadrivalent Pan-Salmonella Vaccine With and Without Alum in Healthy Young Adults

Role: lead

NCT07596173Phase 3Recruiting

A Study on the Immune Response and Safety of a Combined Vaccine Against Diphtheria, Tetanus and Acellular Pertussis (dTpa) in Healthy Japanese Adolescents Aged 11 Years to <13 Years

Role: lead

NCT07221227Phase 3Recruiting

A Pivotal Clinical Study to Investigate Efimosfermin Alfa in Participants With Biopsy-confirmed F2- or F3-stage MASH

Role: lead

NCT07221188Phase 3Recruiting

A Clinical Study to Investigate the Safety and Tolerability of Efimosfermin Alfa Injection in Participants With Known or Suspected F2- or F3-stage MASH

Role: lead

NCT07227311Phase 2Recruiting

A Study to Evaluate the Efficacy and Safety of Belantamab Mafodotin in Combination With Standard of Care in Participants With Relapsed-Refractory Multiple Myeloma (RRMM)

Role: lead

NCT07332455Phase 1Recruiting

First-Time-in-Human Study of GSK5471713 in Adults With mCRPC

Role: lead