🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the EU / 2025-520906-36-00
Authorised Phase II

Microdosing with a serotonergic agent for ADHD and emotion regulation: biological factors explaining and predicting treatment response

2025-520906-36-00 · tracked via the Priya Life Science EU tracker
Sponsor
Universiteit Maastricht
Sponsor type
Educational Institution
Therapeutic area
Mental Disorders
Decision date
11/05/2026
Enrollment target
120
Sites
Netherlands

Condition studied

Attention Deficit Hyperactivity Disorder (ADHD)

Investigational medicinal product(s)

D-lysergic acid diethylamide (LSD)1mL of ethanol95% Vol.

Eligibility

Age group
18-64 years
Sex
Female, Male

Primary endpoint

ADHD symptoms, Emotion regulation, Sleep

Endpoint detail

Pharmacokinetic profile, Theta-beta power ratio, CYP2D6 functionality, Polygenic risk score

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-520906-36-00 on CTIS ↗ ← All trials in the EU