Key Insights

Highlights

Success Rate

88% trial completion (above average)

Published Results

45 trials with published results (24%)

Research Maturity

113 completed trials (61% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

8.6%

16 terminated out of 185 trials

Success Rate

87.6%

+1.1% vs benchmark

Late-Stage Pipeline

32%

60 trials in Phase 3/4

Results Transparency

40%

45 of 113 completed with results

Key Signals

45 with results88% success16 terminated

Data Visualizations

Phase Distribution

150Total
Not Applicable (9)
Early P 1 (2)
P 1 (48)
P 2 (31)
P 3 (44)
P 4 (16)

Trial Status

Completed113
Active Not Recruiting18
Terminated16
Recruiting16
Unknown14
Withdrawn5

Trial Success Rate

87.6%

Benchmark: 86.5%

Based on 113 completed trials

Clinical Trials (185)

Showing 20 of 20 trials
NCT05562947Phase 3RecruitingPrimary

A Study of the Efficacy, Safety, and Pharmacokinetics (PK) of the Port Delivery System With Ranibizumab (PDS) in Chinese Participants With Neovascular Age-related Macular Degeneration (nAMD)

NCT04704921Phase 2Active Not Recruiting

Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administered Via Subretinal Delivery One Time in Participants With nAMD

NCT03683251Phase 3RecruitingPrimary

Extension Study for the Port Delivery System With Ranibizumab (Portal)

NCT06847542Phase 3RecruitingPrimary

A Study of 36-Week Refill Exchanges of Port Delivery System (PDS) With Ranibizumab in nAMD

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

NCT07007065Phase 3RecruitingPrimary

Study to Assess the Injection Burden, Adverse Events, Change in Disease Activity, and Long-Term Preservation of Visual Acuity of Surabgene Lomparvovec in Adult Participants With Neovascular Age-Related Macular Degeneration (nAMD)

NCT04853251Phase 4RecruitingPrimary

A Study Assessing Corneal Endothelial Cells in Participants With Neovascular Age-related Macular Degeneration (nAMD) Treated With the Port Delivery System With Ranibizumab (PDS)

NCT06680817RecruitingPrimary

A Real-World Study to Gain Clinical Insights Into Faricimab (FaReal Study)

NCT05637255Phase 2Completed

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

NCT05476926Active Not RecruitingPrimary

A Real-World Study to Gain Clinical Insights Into Roche Ophthalmology Products

NCT07053358Early Phase 1RecruitingPrimary

Safety and Efficacy Evaluation of LX111 Gene Therapy in nAMD Patients

NCT06196840Phase 2Active Not RecruitingPrimary

Safety and Efficacy of LX102 Gene Therapy in Patients With Neovascular Age-related Macular Degeneration (nAMD) (VENUS)

NCT06723288CompletedPrimary

A Study Conducted to Evaluate the Conjunctiva and Tenon's Capsule Status of Healthy Subjects and in Participants With Neovascular Age-related Macular Degeneration (nAMD)/Diabetic Macular Edema (DME)

NCT06439576Recruiting

Real World Evidence in China: Faricimab Use in Diabetic Macular Edema, Retinal Vein Occlusion, and Neovascular Age-Related Macular Degeneration (The Farseeing Study)

NCT04645212Active Not Recruiting

Long-term Study of ADVM-022 in Neovascular (Wet) AMD [OPTIC-EXT]

NCT04690556Phase 3CompletedPrimary

Study to Compare Efficacy, Safety, and Immunogenicity of LUBT010 (Proposed Ranibizumab Biosimilar) and Lucentis® in Patients With Neovascular AMD

NCT05904028Phase 3RecruitingPrimary

Home OCT-Guided Treatment Versus Treat and Extend for the Management of Neovascular AMD

NCT07275840Phase 2RecruitingPrimary

A Study to Evaluate the Efficacy and Safety of IBI302inSubjects With nAMD

NCT05953012Phase 1CompletedPrimary

Study to Assess Safety and Tolerability of PMC-403 in Subjects With Neovascular Age-related Macular Degeneration

NCT05643118Phase 1CompletedPrimary

Evaluation of OLX10212 in Patients With Neovascular Age-related Macular Degeneration

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