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
- 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.
| Site | City | Country | Site status |
|---|---|---|---|
| Biotrial | Rennes | France | Completed |
This page is information, not medical advice. Discuss any trial with your doctor.