Success Metrics

Clinical Success Rate
83.3%

Based on 5 completed trials

Completion Rate
83%(5/6)
Active Trials
0(0%)
Results Posted
40%(2 trials)
Terminated
1(14%)

Phase Distribution

Ph phase_2
1
14%
Ph phase_3
2
29%
Ph not_applicable
3
43%
Ph phase_1
1
14%

Phase Distribution

1

Early Stage

1

Mid Stage

2

Late Stage

Phase Distribution7 total trials
Phase 1Safety & dosage
1(14.3%)
Phase 2Efficacy & side effects
1(14.3%)
Phase 3Large-scale testing
2(28.6%)
N/ANon-phased studies
3(42.9%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

71.4%

5 of 7 finished

Non-Completion Rate

28.6%

2 ended early

Currently Active

0

trials recruiting

Total Trials

7

all time

Status Distribution
Completed(5)
Terminated(2)

Detailed Status

Completed5
Withdrawn1
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
7
Active
0
Success Rate
83.3%
Most Advanced
Phase 3

Trials by Phase

Phase 11 (14.3%)
Phase 21 (14.3%)
Phase 32 (28.6%)
N/A3 (42.9%)

Trials by Status

withdrawn114%
completed571%
terminated114%

Recent Activity

0 active trials
Showing 5 of 7
completednot_applicable

Cost Evaluation of Venous Leg Ulcers Management

NCT02728986
completedphase_3

Pivotal Trial of Dermagraft(R) to Treat Venous Leg Ulcers

NCT00909870
terminatednot_applicable

Clinical Study to Assess Efficacy and Safety of a New Compression System in the Management of Venous Leg Ulcers

NCT02782689
withdrawnnot_applicable

A Clinical Study to Assess a Compression Device in Patients With Venous Leg Ulcers

NCT02561013
completedphase_1

A Pressure Relted Study Comparing a Compression Device and Profore® on Healthy Volunteers

NCT00821808
View all 7 trials

Clinical Trials (7)

Showing 7 of 7 trials
NCT02728986Not Applicable

Cost Evaluation of Venous Leg Ulcers Management

Completed
NCT00909870Phase 3

Pivotal Trial of Dermagraft(R) to Treat Venous Leg Ulcers

Completed
NCT02782689Not Applicable

Clinical Study to Assess Efficacy and Safety of a New Compression System in the Management of Venous Leg Ulcers

Terminated
NCT02561013Not Applicable

A Clinical Study to Assess a Compression Device in Patients With Venous Leg Ulcers

Withdrawn
NCT00821808Phase 1

A Pressure Relted Study Comparing a Compression Device and Profore® on Healthy Volunteers

Completed
NCT00821431Phase 2

Compression Device Versus 4-layer Compression System

Completed
NCT01891760Phase 3

Long-Term Follow-Up to the DEVO Pivotal Trial of Dermagraft(R) to Treat Venous Leg Ulcers

Completed

All 7 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
7