Retinitis Pigmentosa
210
29
51
101
Key Insights
Highlights
Success Rate
86% trial completion
Published Results
32 trials with published results (15%)
Research Maturity
101 completed trials (48% of total)
Clinical Risk Assessment
Based on trial outcomes
High Risk
Score: 62/100
7.6%
16 terminated out of 210 trials
86.3%
-0.2% vs benchmark
6%
12 trials in Phase 3/4
32%
32 of 101 completed with results
Key Signals
Data Visualizations
Phase Distribution
Trial Status
Trial Success Rate
Benchmark: 86.5%
Based on 101 completed trials
Clinical Trials (210)
Cell Collection to Study Eye Diseases
A First-in-human, Proof of Concept Study of CPK850 in Patients With RLBP1 Retinitis Pigmentosa
A Study of AAV5-hRKp.RPGR for the Treatment of Japanese Participants With X-linked Retinitis Pigmentosa
Retinal Imaging in Patients With Inherited Retinal Degenerations
Rod and Cone Mediated Function in Retinal Disease
A Phase 1/2 Study in Healthy Volunteers and Participants With Autosomal Dominant Retinitis Pigmentosa (RHO-adRP)
Inherited Retinal Degenerative Disease Registry
Promising ROd-cone DYstrophy Gene therapY
Adaptive Optics Imaging of Outer Retinal Diseases
Natural History Study in Patients With PDE6A-, PDE6B- and RHO-linked Retinitis Pigmentosa
High Resolution Retinal Imaging
A Phase I/II Dose-escalating Study of the Safety, Tolerability and Efficacy of KIO-301 Administered Intravitreally to Patients With Retinitis Pigmentosa and Choroideremia (ABACUS)
Oral N-acetylcysteine for Retinitis Pigmentosa
A Phase II Study of Intravitreal KIO-301 in Patients With Late-stage Retinitis Pigmentosa
Natural History Study of Patients With EYS-Associated RP
A Study in Subjects With Retinitis Pigmentosa
A Study to Investigate the Safety of DSP-3077 After a Unilateral Eye Injection in Male and Female Participants 18 Years of Age or Older With Retinitis Pigmentosa
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants
Expanded Access Program for RP in Adults
Natural History of PRPF31 Mutation-Associated Retinal Dystrophy