Jobst Vascular Institute
Toledo, Ohio, 43606, United States
NCT Number: NCT00418483
The purpose of this study is to evaluate the safety of increasing doses of intra-thrombus Plasmin (Human) in acute peripheral arterial occlusion (aPAO). The ability of these Plasmin doses to dissolve the clots will be estimated by arteriography.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
Toledo, Ohio, 43606, United States
There is an unmet need for proven thrombolytic agent in acute peripheral arterial occlusion (aPAO). The current assortment of plasminogen activators are slow to dissolve clots in the leg, and may lead to bleeding complications. Plasmin is a direct thrombolytic that may act more quickly when infused directly into the clot and thus assist in restoring blood flow to the leg. There is a large reserve in blood alpha-2 antiplasmin in the blood to rapidly inactivate Plasmin outside of the clot. Plasmin has the potential for an improved bleeding risk profile in aPAO.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Plasmin (Human) 25 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Other names: TAL-05-00018, BAY-57-9602
Plasmin (Human) 50 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Other names: TAL-05-00018, BAY-57-9602
Plasmin (Human) 75 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Other names: TAL-05-00018, BAY-57-9602
Plasmin (Human) 100 mg
Other names: TAL-05-00018, BAY-57-9602
Plasmin (Human) 125 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Other names: TAL-05-00018, BAY-57-9602
Plasmin (Human) 150 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Other names: TAL-05-00018, BAY-57-9602
Plasmin (Human) 175 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Other names: TAL-05-00018, BAY-57-9602
Time frame: Approximately 5 hours after start of treatment
Thrombolysis at the end of treatment compared to baseline by arteriography
Time frame: Approximately 2 hours after start of treatment
Thrombolysis at 120 minutes compared to baseline by arteriography
Time frame: 30 days
Percent of subjects at Day 30 who avoid open surgical procedures
Time frame: 30 days
Percent of subjects at Day 30 who avoid amputation
Time frame: 30 days
Percent of subjects at Day 30 who avoided additional catheter-directed thrombolysis with a plasminogen activator or mechanical device thrombectomy.
Time frame: 30 days
Percent of subjects at Day 30 who avoided both open surgical procedures and additional thrombolysis with a plasminogen activator or mechanical device thrombectomy.
Time frame: End of treatment, post intervention procedures, Day 1 to 2, Day 7, and Day 30
Physiologic reperfusion defined as improvement in ABI (increase of ≥ 0.15) determined at the end of treatment, post intervention procedures, Day 1 to 2, Day 7, and Day 30.
Time frame: Day 7 and Day 30
Patency assessed by duplex ultrasound imaging on the affected leg on Day 7 and Day 30
Grifols Therapeutics LLC
Industry
A Sequential Phase I/II Dose Escalation and Dose Selection Safety Study of Regional Intra-thrombus Plasmin (Human) Infusion In Acute Lower Extremity Native Artery or Bypass Graft Occlusion
Acronym: PRIORITY
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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