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BMB-101 in Epilepsy With Eyelid Myoclonia (EEM) - Trial NCT06401538

Access comprehensive clinical trial information for NCT06401538 through Pure Global AI's free database. This Phase 2 trial is sponsored by Bright Minds Biosciences Pty Ltd and is currently Not yet recruiting. The study focuses on Jeavons Syndrome. Target enrollment is 20 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06401538
Phase 2
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06401538
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BMB-101 in Epilepsy With Eyelid Myoclonia (EEM)
An Open-Label Phase 2 Study to Evaluate the Efficacy, Safety and Tolerability of BMB-101 in Adolescents and Adults With Epilepsy With Eyelid Myoclonia (EEM; Jeavons Syndrome) Including Those With Prominent Photic Induction (Sunflower Syndrome)

Study Focus

Jeavons Syndrome

BMB-101

Interventional

drug

Sponsor & Location

Bright Minds Biosciences Pty Ltd

Melbourne, Australia

Timeline & Enrollment

Phase 2

Jul 15, 2024

Oct 15, 2025

20 participants

Primary Outcome

Change from baseline in seizure frequency

Summary

The study is a pilot, open-label, study to test whether BMB-101 is safe and effective in
 reducing the frequency of seizures in subjects with Epilepsy with Eyelid Myoclonia (also
 called Jeavons Syndrome). The study will last up to 6 months. There will be a 1 month
 screening period, then 3 months on open-label BMB-101 including titration and
 tapering/washout periods, and then a 1 month follow-up period. There will be 7 clinic visits.

ICD-10 Classifications

Melkersson syndrome
Gilbert syndrome
Crigler-Najjar syndrome
Other histiocytosis syndromes
HELLP syndrome

Data Source

ClinicalTrials.gov

NCT06401538

Non-Device Trial