Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 60/100

Failure Rate

30.0%

6 terminated/withdrawn out of 20 trials

Success Rate

70.0%

-16.5% vs industry average

Late-Stage Pipeline

25%

5 trials in Phase 3/4

Results Transparency

107%

15 of 14 completed trials have results

Key Signals

15 with results5 withdrawn

Enrollment Performance

Analytics

Phase 2
8(40.0%)
Phase 1
7(35.0%)
Phase 3
5(25.0%)
20Total
Phase 2(8)
Phase 1(7)
Phase 3(5)

Activity Timeline

Global Presence

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Clinical Trials (20)

Showing 20 of 20 trials
NCT02563522Phase 3Terminated

Safety and Efficacy Study of Engensis (VM202) in the Treatment of Chronic Non-Healing Foot Ulcers

Role: lead

NCT02427464Phase 3Completed

Phase 3 Gene Therapy for Painful Diabetic Neuropathy

Role: lead

NCT04469270Phase 3Completed

Study to Assess Safety and Efficacy of Engensis in Painful Diabetic Peripheral Neuropathy

Role: lead

NCT04055090Phase 3Completed

Extension of Phase 3 Gene Therapy for Painful Diabetic Neuropathy

Role: lead

NCT04873232Phase 3Completed

A 6-Month Extension Study of VMDN-003-2 to Assess Engensis in Participants With Painful Diabetic Peripheral Neuropathy

Role: lead

NCT02039401Phase 1Completed

Safety Study of VM202 to Treat Amyotrophic Lateral Sclerosis

Role: lead

NCT00696124Phase 1Completed

Safety Study of Gene Therapy in Treating Critical Leg Ischemia

Role: lead

NCT01475786Phase 2Completed

Safety and Efficacy Study for the Treatment of Painful Diabetic Neuropathy

Role: lead

NCT01002235Phase 1Completed

Gene Therapy for Painful Diabetic Neuropathy

Role: lead

NCT05176093Phase 2Completed

A 6-Month Extension Study to Assess the Long-Term Safety of Engensis in Amyotrophic Lateral Sclerosis

Role: lead

NCT04632225Phase 2Completed

Safety of Engensis in Participants With Amyotrophic Lateral Sclerosis

Role: lead

NCT05361031Phase 1Completed

The Safety and Tolerability of Engensis (VM202) in Patients With Charcot-Marie-Tooth Disease Subtype 1A (CMT1A)

Role: lead

NCT01064440Phase 2Completed

Safety and Efficacy Study Using Gene Therapy for Critical Limb Ischemia

Role: lead

NCT01422772Phase 1Completed

Safety Study of Gene Therapy for Ischemic Heart Disease in Korea

Role: lead

NCT00778882Phase 1Withdrawn

Gene Therapy for Chronic Granulomatous Disease in Korea

Role: lead

NCT01002495Phase 1Withdrawn

Gene Therapy for the Treatment of Chronic Stable Angina

Role: lead

NCT03404024Phase 2Withdrawn

Safety and Efficacy Study of Gene Therapy for Acute Myocardial Infarction in Korea

Role: lead

NCT05552625Phase 2Withdrawn

The Efficacy and Safety of TADIOS as an Adjuvant Therapy in Patients Diagnosed With Mild to Moderate COVID-19

Role: lead

NCT01122485Phase 2Withdrawn

Efficacy and Safety Study of PG201 Tablet in Patients With Osteoarthritis

Role: lead

NCT03363165Phase 2Completed

Hepatocyte Growth Factor to Improve Functioning in PAD

Role: collaborator

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