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2024-512196-12-00Not yet recruitingPhase 1

A randomized, placebo-controlled, double-blind, single-ascending-dose, Phase 1a/b study to assess the safety, pharmacokinetics, pharmacodynamics, and immunogenicity of intravenous NTR-641 in healthy adults and patients with acute ischemic stroke

Source: EU CTIS (euclinicaltrials.eu) · Last updated 21 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Next steps

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
72 (estimated)
First submitted
5 Aug 2024
Start date
14 Oct 2024
Lead sponsor
Neutrolis Inc.
Diseases
Stroke
EU CT number
2024-512196-12-00

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 72
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Medical University of ViennaViennaAustriaNot yet recruiting
Krankenhaus Der Barmherzigen Brueder WienViennaAustriaNot yet recruiting

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This page is information, not medical advice. Discuss any trial with your doctor.