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2025-520454-11-00CompletedPhase 1

A study to investigate safety, tolerability, pharmacokinetics and efficacy of REM0045392 compared with placebo in healthy participants

Source: EU CTIS (euclinicaltrials.eu) · Last updated 12 Nov 2025

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
72 (actual)
First submitted
31 Jan 2025
Start date
20 Mar 2025
Lead sponsor
Remynd
EU CT number
2025-520454-11-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 72
  • 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

Are you the coordinator? Confirm the details

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