# Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1)

> **NCT06593951** · — · RECRUITING · sponsor: **Boston Children's Hospital** · enrollment: 200 (estimated)

## Conditions studied

- Progressive Myoclonus Epilepsy Type 1
- EPM1
- CSTB-related Disease
- Myoclonus Epilepsies, Progressive
- Unverricht-Lundborg Disease
- Progressive Epilepsy and/or Ataxia With Myoclonus as a Major Feature
- PME
- Progressive Myoclonus-Epilepsies

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT06593951
- **Lead sponsor:** Boston Children's Hospital
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2024-10-10
- **Primary completion:** 2029-10-01
- **Final completion:** 2030-10-01
- **Target enrollment:** 200 (ESTIMATED)
- **Last updated:** 2026-03-18

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06593951

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06593951, "Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1)". Retrieved via AI Analytics 2026-06-12 from https://api.ai-analytics.org/clinical/NCT06593951. Licensed CC0.

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