跳至主要内容
临床试验/EUCTR2021-002148-56-SK
EUCTR2021-002148-56-SK进行中(未招募)1 期

A RANDOMIZED, DOUBLE BLIND, MULTICENTER, MULTINATIONAL, PLACEBO CONTROLLED, PARALLEL GROUP, SINGLE DOSE, ADAPTIVE EFFICACY AND SAFETY STUDY OF GLENZOCIMAB USED AS AN ADD-ON THERAPY ON TOP OF STANDARD OF CARE IN THE 4.5 HOURS FOLLOWING AN ACUTE ISCHEMIC STROKE - ACTISAVE

ACTICOR BIOTECH0 个研究点目标入组 400 人开始时间: 2021年8月17日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Adult male or female patients = 18 years (i.e., at least 18 years old
  • at time of randomization).
  • 2. Having given their own written consent or legal representative
  • consent or emergency consent, and in any case, in strict accordance with country-specific legal
  • requirements.
  • 3. Presenting with an acute disabling ischemic stroke either in the
  • anterior or in posterior circulation, with or without visible occlusion,
  • with a known time of onset, that is = 4.5 hrs
  • 4. Presenting with a pre-IVT NIHSS = 6
  • 5. In whom IVT is or has been initiated, whether
  • or not patients are additionally eligible to mechanical thrombectomy
  • (MT+IVT), according to the recommendation of the last guidelines (ASA and ESO recommendations)
  • 6. Women of childbearing potential (WOCBP) must have a negative
  • serum/urine pregnancy test at baseline. Women of childbearing
  • potential, i.e, fertile, are defined as women following menarche and until
  • becoming post-menopausal unless permanently sterile, i.e, having
  • undergone hysterectomy, bilateral sal pingectomy and bilateral
  • oophorectomy.
  • 7. Post-menopausal women defined as not having menses for 12 months
  • without an alternative medical cause. For WOCBP, a highly effective birth control method should be in place that can achieve a failure rate of less
  • than 1% per year that should last
  • for at least 2 months after IMP
  • administration.
  • Birth control methods which may be considered as highly effective in
  • WOCBP include:
  • - combined (estrogen and progestogen containing) hormonal
  • contraception associated with inhibition of ovulation (intravaginal,
  • transdermal),
  • - progestogen-only hormonal contraception associated with inhibition of
  • ovulation (injectable, implantable)
  • - intrauterine device (IUD),
  • - intrauterine hormone-releasing system (IUS),
  • - bilateral tubal occlusion,
  • - vasectomized partner,
  • Birth control methods which may be considered as highly effective for
  • men and that should last for 4 months after IMP administration include:
  • - vasectomy,
  • - use of condom combined with a highly effective birth control method
  • for their WOCBP partner.
  • Please note that hormonal contraception is a risk factor for
  • thromboembolic events and attention should be called to reconsider it
  • passed the acute stroke phase.
  • 8. Patients affiliated to a health insurance – modality depending on
  • country legal requirement
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 133
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 267

排除标准

  • 1. Coma, or NIHSS >25
  • 2. Patients < 18 years
  • 3. Protected adults under guardianship or curatorship
  • 4. Prior ischemic stroke within the past 3 months
  • 5. mRS pre-stroke known to be = 2
  • 6. Large (more than 1/3 of the middle cerebral artery) regions of clear
  • hypodensity on Baseline Computed Tomography Angiography (CTA) or
  • Magnetic Resonance Imaging (MRI) or with vascular injection (MRA).
  • 7. Significant mass effect with midline shift
  • 8. Stroke of hemorrhagic origin
  • 9. Patients likely to require dual antiplatelet therapy (DAPT) within the
  • first 24 hrs after cessation of glenzocimab or placebo infusion for e.g.,
  • carotid stenting
  • 10. Known renal insufficiency (Grades 4-5 – severe or terminal)
  • creatinine clearance < 30 mL/Mn using Cockroft formula)
  • 11. Known allergic reaction to contrast agents
  • 12. Patients under anti-coagulant therapy, except preventative doese of
  • injectable low molecular weight heparin (LMWH).
  • 13. Known ongoing treatment with a mAb.
  • 14. Prior cardiopulmonary resuscitation < 10 days.
  • 15. Childbirth within < 10 days.
  • 16. eizures at stroke onset if it precludes obtaining an accurate
  • baseline (pre-IVT)NIHSS,
  • 17. Life expectancy (except for stroke) < 3 months.
  • 18. Pregnancy or breastfeeding.
  • 19. Females of childbearing potential not using effective birth control methods.
  • 20. Known current participation in another clinical investigation with experimental drug.

研究者

相似试验

进行中(未招募)
1 期
ADAPTIVE EFFICACY AND SAFETY STUDY OF GLENZOCIMAB USED AS AN ADD-ON THERAPY ON TOP OF STANDARD OF CARE IN THE 4.5 HOURS FOLLOWING AN ACUTE ISCHEMIC STROKEAcute ischemic strokeMedDRA version: 22.1Level: LLTClassification code 10055221Term: Ischemic strokeSystem Organ Class: 100000004852
EUCTR2021-002148-56-FRACTICOR BIOTECH1,000
进行中(未招募)
1 期
ADAPTIVE EFFICACY AND SAFETY STUDY OF GLENZOCIMAB USED AS AN ADD-ON THERAPY ON TOP OF STANDARD OF CARE IN THE 4.5 HOURS FOLLOWING AN ACUTE ISCHEMIC STROKEAcute ischemic strokeMedDRA version: 22.1Level: LLTClassification code 10055221Term: Ischemic strokeSystem Organ Class: 100000004852
EUCTR2021-002148-56-DEACTICOR BIOTECH400
进行中(未招募)
1 期
ADAPTIVE EFFICACY AND SAFETY STUDY OF GLENZOCIMAB USED AS AN ADD-ON THERAPY ON TOP OF STANDARD OF CARE IN THE 4.5 HOURS FOLLOWING AN ACUTE ISCHEMIC STROKEAcute ischemic strokeMedDRA version: 22.1Level: LLTClassification code 10055221Term: Ischemic strokeSystem Organ Class: 100000004852
EUCTR2021-002148-56-ESACTICOR BIOTECH1,000
进行中(未招募)
1 期
ADAPTIVE EFFICACY AND SAFETY STUDY OF GLENZOCIMAB USED AS AN ADD-ON THERAPY ON TOP OF STANDARD OF CARE IN THE 4.5 HOURS FOLLOWING AN ACUTE ISCHEMIC STROKE
EUCTR2021-002148-56-DKACTICOR BIOTECH400
进行中(未招募)
1 期
ADAPTIVE EFFICACY AND SAFETY STUDY OF GLENZOCIMAB USED AS AN ADD-ON THERAPY ON TOP OF STANDARD OF CARE IN THE 4.5 HOURS FOLLOWING AN ACUTE ISCHEMIC STROKEAcute ischemic strokeMedDRA version: 22.1Level: LLTClassification code 10055221Term: Ischemic strokeSystem Organ Class: 100000004852
EUCTR2021-002148-56-CZACTICOR BIOTECH1,000