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NCT07016464

A Study to Investigate Safety, Tolerability and Pharmacokinetics of REM0045392 Compared With Placebo in Healthy Participants.

Terminated Phase 1 Last updated 4 February 2026
What this trial tests

Phase 1 trial testing REM0045392 in Healthy in 19 participants. Terminated before completion.

Timeline
20 March 2025
Primary endpoint
23 June 2025
23 June 2025

Quick facts

Lead sponsorreMYND
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingquadruple
Primary purposetreatment
Enrollment19
Start date20 March 2025
Primary completion23 June 2025
Estimated completion23 June 2025
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

reMYND — full company profile →

Who can join

Adults 18 to 85, any sex, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is testing if the medicine REM0045392 is safe and well-tolerated. It also looks at whether food affects how the medicine works. The medicine will be tested in Healthy men (Part 1 and 2) and Healthy Older men and women (Part 3). Participants will take the medicine once (in Part 1) or during 14 days (in Part 2 and 3), with increasing doses. REM0045392 is being developed as a treatment for Alzheimer's disease.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Alzheimer's disease drug development pipeline: 2026.
    Cummings JL, Zhou Y, Yang Y, Zhong K, et al · · 2026 · PMID 42095064 · DOI 10.1002/trc2.70251

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Other recruiting trials for Healthy

Currently open trials in the same condition.

Other reMYND trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07016464.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing