Clin2
NCT06401538Possibly a fitRecruiting

BMB-101 for absence epilepsy and DEE

Absence EpilepsyJeavons SyndromeDravet SyndromeLennox Gastaut Syndrome

Part of Brain & nervous system, Genetic & congenital clinical trials.

This trial tests a new drug called BMB-101 for people with absence epilepsy (including Jeavons syndrome) or developmental epileptic encephalopathies (DEE) like Dravet or Lennox-Gastaut. It aims to see if the drug can reduce seizure frequency and is safe.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
20 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You have a diagnosis of absence epilepsy (with or without eyelid jerks) or a developmental and epileptic encephalopathy (DEE) like Dravet or Lennox-Gastaut.
  • You are between 18 and 65 years old.
  • You have tried at least one seizure medicine and have been on a stable dose of your current seizure medicines for at least 4 weeks.
  • You are willing to use effective birth control if you or your partner could become pregnant, and for 90 days after the last dose.
  • You do not have serious heart, liver, or kidney problems, or a history of stroke or heart attack.
  • You are not currently taking certain medications like fenfluramine, antidepressants, or antipsychotics.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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