Key Insights

Highlights

Success Rate

87% trial completion (above average)

Published Results

12 trials with published results (24%)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

10.0%

5 terminated out of 50 trials

Success Rate

87.2%

+0.7% vs benchmark

Late-Stage Pipeline

34%

17 trials in Phase 3/4

Results Transparency

35%

12 of 34 completed with results

Key Signals

12 with results87% success

Data Visualizations

Phase Distribution

37Total
Not Applicable (3)
P 1 (1)
P 2 (16)
P 3 (9)
P 4 (8)

Trial Status

Completed34
Terminated5
Unknown5
Recruiting2
Active Not Recruiting2
Withdrawn1

Trial Success Rate

87.2%

Benchmark: 86.5%

Based on 34 completed trials

Clinical Trials (50)

Showing 20 of 20 trials
NCT07440225Phase 2Recruiting

A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-002)

NCT07496567Phase 2Recruiting

A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-003)

NCT05112861Phase 3Active Not Recruiting

A 3-month Study to Compare the Safety of ONS-5010 in Vials Versus Pre-filled Syringe in Subjects With Visual Impairment Due to Retinal Disorders

NCT05637255Phase 2CompletedPrimary

A Randomized, Double Masked, Parallel Group, Dose-finding Study to Evaluate SYL1801 in Patients With Neovascular Age-related Macular Degeneration (AMD)

NCT03823287Phase 3CompletedPrimary

A Study to Evaluate the Efficacy and Safety of Faricimab in Participants With Neovascular Age-Related Macular Degeneration (TENAYA)

NCT03823300Phase 3CompletedPrimary

A Study to Evaluate the Efficacy and Safety of Faricimab in Participants With Neovascular Age-Related Macular Degeneration (LUCERNE)

NCT04420923Not ApplicableActive Not RecruitingPrimary

Optimizing the Treatment Strategy for Age-related Macular Degeneration

NCT03834753Phase 3Completed

A Clinical Effectiveness Study Examining the Efficacy and Safety of ONS-5010 in Subjects With Neovascular Age-related Macular Degeneration (AMD)

NCT04516278Phase 3Completed

A 3-month Study to Assess the Safety of ONS-5010 in Subjects With Visual Impairment Due to Retinal Disorders

NCT03844074Phase 3Completed

A Clinical Effectiveness Study Examining the Efficacy and Safety of ONS-5010 in Subjects With Neovascular Age-related Macular Degeneration (AMD)

NCT06190093Phase 3Completed

A 3-month Study to Assess the Safety and Effectiveness of ONS-5010 in Subjects with Neovascular Age-related Macular Degeneration (AMD)

NCT03861234Phase 1CompletedPrimary

A Study to Test Different Doses of BI 836880 in Patients With an Eye Disease Called Wet Age-related Macular Degeneration (wAMD)

NCT04832724Phase 2Completed

RGX-314 Gene Therapy Pharmacodynamic Study for Neovascular Age-related Macular Degeneration (nAMD)

NCT04049266Phase 2TerminatedPrimary

A Study to Evaluate the Efficacy and Safety of KSI-301, an Anti-VEGF Antibody Biopolymer Conjugate, Versus Aflibercept in Patients With Neovascular (Wet) Age-Related Macular Degeneration.

NCT03999801Phase 2Enrolling By Invitation

Long-term Follow-Up Study of RGX-314 and Fellow Eye Substudy

NCT05211804CompletedPrimary

Mechanisms of Retinal Revascularization and Clinical Indicators of Neovascular AMD Relapse

NCT02305238Phase 4CompletedPrimary

Japanese Treat and Extend Study of Aflibercept in Neovascular Age-related Macular Degeneration

NCT02279537CompletedPrimary

Real Life of Aflibercept In FraNce: oBservatiOnnal Study in Wet AMD

NCT02289924CompletedPrimary

Aflibercept (Eylea) in roUtine Clinical Practice in patientS With Wet Age-related Macular Degeneration in Italy

NCT05675540UnknownPrimary

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