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Safety, pharmacokinetics and pharmacodynamics study of Leucettinib-21 in healthy subjects, Down Syndrom and Alzheimer patients

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-507075-22-00
Enrollment
140
Registered
2023-12-13
Start date
2024-01-05
Completion date
Unknown
Last updated
2026-01-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

and patients with Alzheimer’s disease, A Phase 1, Double-Blind, First in Human Study to Evaluate the Safety, followed by an open single dose of Leucettinib-21 in Down Syndrome individuals, Pharmacokinetics and Pharmacodynamics of Single and Multiple Ascending Doses and Food Effect of Leucettinib-21 in Healthy Male Subjects, Placebo-Controlled, Randomized, Tolerability

Interventions

None listed

Sponsors

Eurofins Optimed, Perha Pharmaceuticals
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026