BMB-101 in Epilepsy With Eyelid Myoclonia (EEM)
- Disease/Condition
- Jeavons Syndrome
- Drug/Device/Intervention
- BMB-101
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Bright Minds Biosciences Pty Ltd
- Location
- Melbourne, Australia
- Phase
- Phase 2
- Start date
- Jul 15, 2024
- End date
- Oct 15, 2025
- Enrollment
- 20 participants
Change from baseline in seizure frequency
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06401538
- Type
- Non-Device Trial
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.