Key Insights

Highlights

Success Rate

86% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 62/100

Termination Rate

4.2%

1 terminated out of 24 trials

Success Rate

85.7%

-0.9% vs benchmark

Late-Stage Pipeline

4%

1 trials in Phase 3/4

Results Transparency

17%

1 of 6 completed with results

Key Signals

1 with results86% success

Data Visualizations

Phase Distribution

15Total
Not Applicable (5)
Early P 1 (1)
P 2 (8)
P 4 (1)

Trial Status

Recruiting12
Completed6
Not Yet Recruiting2
Terminated1
Unknown1
Active Not Recruiting1

Trial Success Rate

85.7%

Benchmark: 86.6%

Based on 6 completed trials

Clinical Trials (24)

Showing 20 of 20 trials
NCT07756242WithdrawnPrimary

Pharmacokinetic Study of Therapeutic Plasma Exchange

NCT07663422Phase 2Recruiting

Mycophenolate Mofetil w/ Prednisone for Immune Related Hepatitis From Checkpoint Inhibitor Therapy

NCT05700565CompletedPrimary

Treatment of Immune-related Adverse Events Refractory to Standard Therapy and Associated Changes in Immunophenotype

NCT03948724Not ApplicableCompleted

Impact of Therapeutic Patient Education on the Toxicity of Immune Checkpoint Inhibitors in Oncology

NCT06337695Phase 2Recruiting

Vedolizumab for the Prevention of ICI Related Diarrhea or Colitis in Patients With Cancer

NCT06860542Phase 2Recruiting

Inhaled Budesonide for REcurrence Prevention and Adjuvant THerapy in Checkpoint Inhibitor Pneumonitis

NCT04305145Phase 2Active Not Recruiting

Infliximab for Treatment of Immune Checkpoint Inhibitor Colitis

NCT07644897Phase 2Recruiting

Thymosin Alpha 1 Combined With Anti-PD-1 Monoclonal Antibody in Elderly Patients With Advanced Melanoma

NCT06037811Phase 2Recruiting

Early Adalimumab Induction for Immune Checkpoint Inhibitor Associated Inflammatory Arthritis

NCT05544292CompletedPrimary

Rheumatic IMmune-Related Adverse Events in Patients Treated With Immune Check Point Inhibitors

NCT05663775Phase 2RecruitingPrimary

Prophylactic Mesalamine to Prevent Colitis Following Treatment With Ipilimumab/Nivolumab (Ipi/Nivo)

NCT06440811CompletedPrimary

Efficacy and Safety of Neoadjuvant Nivolumab Plus SOX Versus Nivolumab Plus FLOT in Patients With HER2-negative Gastric and Gastroesophageal Junction Adenocarcinoma

NCT05813418Not ApplicableRecruiting

Identification of Predictive Biomarkers for Immune-Related Adverse Events (irAEs) in Patients Undergoing Immune CheckPoint Inhibitors (ICPI) Treatment

NCT06908018Early Phase 1Not Yet Recruiting

Safety, Virological and Immunological Assessment of the Controlled Dengue Human Infection Model in Dengue-Immune Participants in Thailand (DHIT-Immune)

NCT05832606Not ApplicableRecruitingPrimary

Food Intervention to Reduce Immunotherapy ToXicity

NCT05699915Not ApplicableTerminated

Extensive CArdioVAscular Characterization and Follow-up of Patients Receiving Immune Checkpoint Inhibitors

NCT06089967Completed

Immune-Related Adverse Events and Associated Biomarkers in Patients Receiving Cancer Immunotherapy

NCT06785974Phase 4Not Yet Recruiting

Statins to Prevent Immune Checkpoint Inhibitor-induced PRogression of AtherosLerosis

NCT06613165RecruitingPrimary

Exploring the Treatment Duration of PD-1 Neoadjuvant Therapy in Stage II-III dMMR Rectal Cancer

NCT06278857Phase 2Recruiting

SATELLITE Study (feaSibility sAfeTy Efficacy dostarLimab earLy-stage defIcient endomeTrial cancEr)

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