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WithdrawnNCT05921929

First-in-human FENM study in healthy adults

The withdrawn trial planned to study the safety and processing of a single oral dose.

Medication studyAges 18–45BelgiumDepression
The study in practice

Understand this study

Who could participate?

This withdrawn early-phase study was designed for healthy adult volunteers aged 18 to 45.

What does the protocol involve?

The protocol planned one oral dose of FENM per participant to study safety and how the body processes the drug.

Listed locations
LiègeSee all locations and recruitment
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: May 2, 2024
Recruitment status
Withdrawn
Enrollment listed in the registry
0
Sponsor
ReST Therapeutics
Sponsor type
Biotech company
Study type
Drug
Intervention type
Drug
Study phase
Phase 1Usually an early study focused on safety, tolerability, dosage, and side effects.
Locations
Belgium
Age range
From 18 Years to 45 Years
Official registry ID
NCT05921929
Official title
Show the full official title

Safety and Pharmacokinetics of a Novel NMDA Receptor Antagonist Against Brain Related Diseases in Healthy Adult Volunteers: First-in-human, Phase I, Single Dose-escalating, Open Label Study

Recruitment & locations

Withdrawn

Liège

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Updated by the registry

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is ReST Therapeutics.

Does this study involve medication?

Yes. The study involves medication, including Fluoroethylnormemantine (FENM).

Who could participate?

This withdrawn early-phase study was designed for healthy adult volunteers aged 18 to 45.

Is this study still recruiting?

The registry lists this study as withdrawn.

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