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Completed

NCT Number: NCT00418483

A Dose Escalation and Safety Study of Plasmin (Human) In Acute Lower Extremity Native Artery or Bypass Graft Occlusion

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Jobst Vascular Institute

Toledo, Ohio, 43606, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years.
  • Women of childbearing potential must use adequate contraception for the duration of the study and must have a negative pregnancy test prior to study entry.
  • Unilateral limb ischemia: SVS acute ischemia Category I or IIa.
  • Onset of symptoms </= 14 days.
  • Thrombosed (non-embolic) infrainguinal graft (synthetic, autologous, or single outflow composite) or infrainguinal native artery. For native arteries, only occlusions of ≥ 10 cm in length are eligible.
  • Diagnosis of occlusive thrombus in the graft or artery by arteriography after Informed Consent is obtained.
  • Ability to traverse the thrombus with a guidewire.
  • Signed informed consent prior to study entry.

Exclusion criteria

  • Clinical evidence of significant disease that may interfere with the patient successfully completing the trial.
  • Women who are pregnant or lactating, or first 10 days post-partum.
  • Previous hemorrhagic stroke at any time. Thrombotic or embolic stroke or cerebrovascular events (including transient ischemic attack (TIA)) within one year.
  • Intracranial or spinal neuro-surgery, or severe intracranial trauma in the last 3 months. Major surgery, organ biopsy, or major trauma within the last 10 days. Lumbar puncture or non-compressible arterial puncture in the last 10 days. Intra-ocular surgery within the last 10 days.
  • Current bleeding diathesis. Active gastrointestinal or organ bleeding. Minor bleeding such as normal menses, cystitis, or minor hemorrhoidal bleeding are not exclusions.
  • Uncontrolled arterial hypertension, defined as a systolic blood pressure > 180 mmHg or diastolic blood pressure > 110 mmHg.
  • Known intracranial neoplasm, aneurysm, or arterio-venous malformation.
  • Platelet count < 75 x 10e9/L.
  • Occlusion of a graft within 6 months of placement.
  • Medically unable to tolerate an open vascular procedure.
  • Known prothrombotic condition.
  • Hemoglobin <10.0 g/dL
  • Impaired renal function or renal disease that constitutes a contraindication to contrast angiography, including creatinine > 2.0 mg/dL or subjects on renal dialysis.
  • Treatment with a glycoprotein IIb/IIIa class of platelet inhibitor within the past 5 days, for example, abciximab (ReoPro®), eptifibatide (Integrilin®) or tirofiban (Aggrastat®).
  • Treatment with warfarin (Coumadin®) and with an INR of >1.7 (elevated INR at screening may be corrected prior to study enrollment.)

Treatment and study plan

Plasmin (Human) 25 mg

Biological

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

Biological

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

Biological

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

Biological

Plasmin (Human) 100 mg

Other names: TAL-05-00018, BAY-57-9602

Plasmin (Human) 125 mg

Biological

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

Biological

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

Biological

Plasmin (Human) 175 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.

Other names: TAL-05-00018, BAY-57-9602

Primary outcomes

  1. Thrombolysis

    Time frame: Approximately 5 hours after start of treatment

    Thrombolysis at the end of treatment compared to baseline by arteriography

Secondary outcomes

  1. Thrombolysis

    Time frame: Approximately 2 hours after start of treatment

    Thrombolysis at 120 minutes compared to baseline by arteriography

  2. Avoidance of open surgical procedures

    Time frame: 30 days

    Percent of subjects at Day 30 who avoid open surgical procedures

  3. Avoidance of amputation

    Time frame: 30 days

    Percent of subjects at Day 30 who avoid amputation

  4. Avoidance of additional catheter-directed thrombolysis with a plasminogen activator or mechanical device thrombectomy

    Time frame: 30 days

    Percent of subjects at Day 30 who avoided additional catheter-directed thrombolysis with a plasminogen activator or mechanical device thrombectomy.

  5. Avoidance of both open surgical procedures and additional 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.

  6. Physiologic reperfusion defined as improvement in ankle brachial index (ABI)

    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.

  7. Patency assessed by duplex ultrasound imaging

    Time frame: Day 7 and Day 30

    Patency assessed by duplex ultrasound imaging on the affected leg on Day 7 and Day 30

Sponsors and collaborators

Lead sponsor

Grifols Therapeutics LLC

Industry

Registry information

Official study title

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

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Jan 4, 2007
Registry last updated
Oct 31, 2016

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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