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2025-522571-28-00CompletedPhase 1

A study to evaluate how well single and multiple doses of O3R-5671-PRO are tolerated in healthy adult subjects

Source: EU CTIS (euclinicaltrials.eu) · Last updated 15 Jul 2026

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
96 (actual)
First submitted
1 Jul 2025
Start date
28 Aug 2025
Lead sponsor
Coultreon Biopharma
EU CT number
2025-522571-28-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 96
  • 1 site 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 (1)

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

SiteCityCountrySite status
SGS BelgiumEdegemBelgiumCompleted

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