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Active, not recruiting Phase 2 Interventional

An Open-Label Extension Study of STK-001 for Patients With Dravet Syndrome

ClinicalTrials.gov ID: NCT04740476

Public ClinicalTrials.gov record NCT04740476. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:23 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label Extension Study for Patients With Dravet Syndrome Who Previously Participated in Studies of STK-001

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Stoke Therapeutics is evaluating the long-term safety \& tolerability of repeated doses of zorevunersen (STK-001) in patients with Dravet syndrome who previously participated in studies of zorevunersen. Change in seizure frequency and overall clinical status, and quality of life will be measured as secondary endpoints in this open-label study.

Study identification

NCT ID
NCT04740476
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Stoke Therapeutics, Inc
Industry
Enrollment
60 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
30 Months and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 20, 2021 (Actual)
Primary completion
Mar 31, 2029 (Estimated)
Completion
Mar 31, 2029 (Estimated)
Last update posted
Feb 4, 2026

2021 – 2029

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
University of California San Francisco Medical Center San Francisco California 94158 —
Children's Hospital Colorado Aurora Colorado 80045 —
Children's National Medical Center Washington D.C. District of Columbia 20010 —
Nicklaus Children's Hospital Miami Florida 33155 —
Florida Hospital for Children Orlando Florida 32803 —
Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois 60611 —
University of Iowa Children's Hospital Iowa City Iowa 52242 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Michigan Medicine Ann Arbor Michigan 48109 —
Mayo Clinic Rochester Minnesota 55905 —
NYU Comprehensive Epilepsy Center New York New York 10016 —
Oregon Health & Science University Portland Oregon 97239 —
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104 —
UT LeBonheur Pediatric Specialists, Inc. Memphis Tennessee 38103 —
Cook Children's Medical Center Fort Worth Texas 76104 —
Seattle Children's Hospital Seattle Washington 98105 —
MultiCare Health System Institute for Research and Innovation Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04740476, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 4, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04740476 live on ClinicalTrials.gov.

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