Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

5.0%

1 terminated/withdrawn out of 20 trials

Success Rate

94.4%

+7.9% vs industry average

Late-Stage Pipeline

10%

2 trials in Phase 3/4

Results Transparency

18%

3 of 17 completed trials have results

Key Signals

1 recruiting3 with results

Enrollment Performance

Analytics

Phase 2
6(35.3%)
N/A
5(29.4%)
Phase 1
4(23.5%)
Phase 3
2(11.8%)
17Total
Phase 2(6)
N/A(5)
Phase 1(4)
Phase 3(2)

Activity Timeline

Global Presence

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Clinical Trials (20)

Showing 20 of 20 trials
NCT06034379Not ApplicableRecruiting

Electronic Spectacles Versus Low Dose Atropine in Young Myopes

Role: lead

NCT06085430Not ApplicableCompleted

Kubota Glass Parameter Refinement Study

Role: lead

NCT03772665Phase 3Completed

Safety and Efficacy of Emixustat in Stargardt Disease

Role: lead

NCT05425108Not ApplicableUnknown

Binocular Peripheral Myopic Defocus Using a Clinical Prototype Device

Role: lead

NCT04415684Not ApplicableCompleted

Projected Peripheral Defocus Using a Wearable Device

Role: lead

NCT04388020Not ApplicableCompleted

Effects of Projected Peripheral Defocus on Ocular Biometrics

Role: lead

NCT02753400Phase 2Completed

Study to Evaluate Effects of Emixustat Hydrochloride in Subjects With Proliferative Diabetic Retinopathy

Role: lead

NCT03033108Phase 2Completed

Pharmacodynamic Study of Emixustat Hydrochloride in Subjects With Macular Atrophy Secondary to Stargardt Disease

Role: lead

NCT04428242Withdrawn

Study Evaluating Retinal Health Monitoring System Thickness Module

Role: lead

NCT04169802Completed

Study Evaluating Retinal Health Monitoring System Visual Acuity Module.

Role: lead

NCT04499703Completed

Evaluation of the Retinal Health Monitoring System Thickness Module

Role: lead

NCT01802866Phase 2Completed

Safety and Efficacy Assessment Treatment Trials of Emixustat Hydrochloride

Role: lead

NCT02130531Phase 1Completed

Pharmacokinetic and Pharmacodynamic Study of Emixustat in Subjects With Geographic Atrophy Associated With Dry Age-Related Macular Degeneration

Role: lead

NCT01632137Phase 3Completed

Efficacy and Safety of Rebamipide in Subjects With Dry Eye Syndrome

Role: lead

NCT01410188Phase 1Completed

Safety/Efficacy Study: OPA-6566 Ophthalmic Solution in Subjects With Primary Open-Angle Glaucoma or Ocular Hypertension

Role: lead

NCT01002950Phase 2Completed

Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ACU-4429 in Subjects With Geographic Atrophy

Role: lead

NCT00703183Phase 1Completed

Safety and Tolerability of ACU-4429

Role: lead

NCT01057147Phase 2Completed

Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Subjects With Dry Eye - Effects on Central Cornea

Role: lead

NCT01027013Phase 2Completed

Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Patients With Dry Eye

Role: lead

NCT00942240Phase 1Completed

Safety and Tolerability of Repeat Doses of ACU-4429 in Healthy Subjects

Role: lead

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