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2024-512330-15-00CompletedPhase 1

Phase I, first-in-man, randomised, placebo-controlled, single dose escalation study to investigate the effects of LPH-5 on safety, tolerability, pharmacokinetic and pharmacodynamic parameters in healthy participants

Source: EU CTIS (euclinicaltrials.eu) · Last updated 1 Aug 2025

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
56 (actual)
First submitted
31 May 2024
Start date
5 Aug 2025
Lead sponsor
Lophora ApS
EU CT number
2024-512330-15-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 56
  • 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
BiotrialRennesFranceCompleted

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