Evaluation of MST-188 in Acute Lower Limb Ischemia
Status: | Terminated |
---|---|
Conditions: | Peripheral Vascular Disease |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 30 - 80 |
Updated: | 4/21/2016 |
Start Date: | June 2014 |
Evaluation of MST-188 in Acute Lower Limb Ischemia: A Phase 2 Randomized, Double-Blind, Placebo-Controlled, Multi-Center Clinical Trial Evaluating the Safety and Efficacy of MST-188 in Subjects With Acute Lower Limb Ischemia Receiving Catheter-Directed Recombinant Tissue Plasminogen Activator
The purpose of this study is to evaluate the safety and efficacy of MST-188 in subjects
receiving catheter-directed rt-PA for acute lower limb ischemia and to evaluate whether
treatment with MST-188 results in more rapid thrombolysis of the occlusion and more rapid
tissue perfusion in the effected blood vessel.
receiving catheter-directed rt-PA for acute lower limb ischemia and to evaluate whether
treatment with MST-188 results in more rapid thrombolysis of the occlusion and more rapid
tissue perfusion in the effected blood vessel.
Inclusion Criteria:
- Age ≥30 to <80
- Symptoms consistent with ALI in target lower limb classified as Rutherford Category
IIa or IIb
- Subject is hospitalized or in the process of hospitalization for the treatment of ALI
- Angiographic confirmation of thrombotic lower limb arterial occlusion
Exclusion Criteria:
- Prosthetic bypass graft occlusion within 1 month of implantation or autogenous graft
occlusion within 6 months of placement
- Treatment with a thrombolytic agent within the last 48 hours
- Subject's laboratory results indicate inadequate organ function
- NYHA Class IV congestive heart failure
- Prior major amputation of the target limb
- Other complications or contraindications for receiving rt-PA, anticoagulants, or
contrast media
We found this trial at
4
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials