Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

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

28. oktober 2016 opdateret af: Grifols Therapeutics LLC

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

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.

Studieoversigt

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

83

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Ohio
      • Toledo, Ohio, Forenede Stater, 43606
        • Jobst Vascular Institute

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

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.)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Plasmin (Human) 25 mg
Plasmin (Human) 25 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Andre navne:
  • TAL-05-00018
  • BAY-57-9602
Eksperimentel: Plasmin (Human) 50 mg
Plasmin (Human ) 50 mg
Plasmin (Human) 50 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Andre navne:
  • TAL-05-00018
  • BAY-57-9602
Eksperimentel: Plasmin (Human) 75 mg
Plasmin (Human) 75 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Andre navne:
  • TAL-05-00018
  • BAY-57-9602
Eksperimentel: Plasmin (Human) 100 mg
Plasmin (Human) 100 mg
Andre navne:
  • TAL-05-00018
  • BAY-57-9602
Eksperimentel: Plasmin (Human) 125 mg
Plasmin (Human) 125 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Andre navne:
  • TAL-05-00018
  • BAY-57-9602
Eksperimentel: Plasmin (Human) 150 mg
Plasmin (Human) 150 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Andre navne:
  • TAL-05-00018
  • BAY-57-9602
Eksperimentel: Plasmin (Human) 175 mg
Plasmin (Human) 175 mg delivered via an infusion catheter into the thrombus over approximately 5 hours.
Andre navne:
  • TAL-05-00018
  • BAY-57-9602

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Thrombolysis
Tidsramme: Approximately 5 hours after start of treatment
Thrombolysis at the end of treatment compared to baseline by arteriography
Approximately 5 hours after start of treatment

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Thrombolysis
Tidsramme: Approximately 2 hours after start of treatment
Thrombolysis at 120 minutes compared to baseline by arteriography
Approximately 2 hours after start of treatment
Avoidance of open surgical procedures
Tidsramme: 30 days
Percent of subjects at Day 30 who avoid open surgical procedures
30 days
Avoidance of amputation
Tidsramme: 30 days
Percent of subjects at Day 30 who avoid amputation
30 days
Avoidance of additional catheter-directed thrombolysis with a plasminogen activator or mechanical device thrombectomy
Tidsramme: 30 days
Percent of subjects at Day 30 who avoided additional catheter-directed thrombolysis with a plasminogen activator or mechanical device thrombectomy.
30 days
Avoidance of both open surgical procedures and additional thrombolysis with a plasminogen activator or mechanical device thrombectomy.
Tidsramme: 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.
30 days
Physiologic reperfusion defined as improvement in ankle brachial index (ABI)
Tidsramme: 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.
End of treatment, post intervention procedures, Day 1 to 2, Day 7, and Day 30
Patency assessed by duplex ultrasound imaging
Tidsramme: Day 7 and Day 30
Patency assessed by duplex ultrasound imaging on the affected leg on Day 7 and Day 30
Day 7 and Day 30

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Anthony J Comerota, MD, Jobst Vascular Center

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. marts 2007

Primær færdiggørelse (Faktiske)

1. april 2010

Studieafslutning (Faktiske)

1. april 2010

Datoer for studieregistrering

Først indsendt

2. januar 2007

Først indsendt, der opfyldte QC-kriterier

2. januar 2007

Først opslået (Skøn)

4. januar 2007

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

31. oktober 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

28. oktober 2016

Sidst verificeret

1. oktober 2016

Mere information

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner