NCT06401538

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)
Bright Minds Biosciences Pty Ltd·Phase 2·ClinicalTrials.gov·drugNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Jeavons Syndrome
Drug/Device/Intervention
BMB-101
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Bright Minds Biosciences Pty Ltd
Location
Melbourne, Australia
Timeline & enrollment
Phase
Phase 2
Start date
Jul 15, 2024
End date
Oct 15, 2025
Enrollment
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 syndromeGilbert syndromeCrigler-Najjar syndromeOther histiocytosis syndromesHELLP syndrome
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06401538
Type
Non-Device Trial
About this record

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.