A Study of Soticlestat as an Add-on Therapy in Children and Young Adults With Dravet Syndrome

Last updated:
2026-09-05
Language and content disclaimer

The content and search results on this site are collected from or provided by third parties. As such some of the information may only be available in the language originally submitted by the sponsor of the trial. Learn more about the information on the search portal.

Linking to Non-Government of Canada Websites

Links to websites not under the control of the Government of Canada, including those to our social media accounts, and to clinical trial records in international registries are provided solely for the convenience of our website visitors. We are not responsible for the accuracy, currency or reliability of the content of such websites. The Government of Canada does not offer any guarantee in that regard and is not responsible for the information found through these links, nor does it endorse the sites and their content.

Visitors should also be aware that information offered by non-Government of Canada sites to which this website links is not subject to the Privacy Act or the Official Languages Act and may not be accessible to persons with disabilities. The information offered may be available only in the language(s) used by the sites in question. With respect to privacy, visitors should research the privacy policies of these non-government websites before providing personal information.

View trial details

Overview

Official protocol title:

A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP STUDY TO EVALUATE THE EFFICACY, SAFETY, AND TOLERABILITY OF SOTICLESTAT AS ADJUNCTIVETHERAPY IN PEDIATRIC AND YOUNG ADULT SUBJECTS WITH DRAVET SYNDROME (DS)

Intervention/treatment:
SOTICLESTAT (TAK-935)
Medical condition:
DRAVET SYNDROME
Protocol code:
TAK-935-3001
Control number:
254307
Status:
Closed
Approved:
July 29, 2021
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT04940624
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
2 Years to 21 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Study Director
Organization
Takeda (Note: This product was divested to Mistrau Bio, Inc. in 2026)
Phone:
+1-877-825-3327
Sponsor
TAKEDA DEVELOPMENT CENTER AMERICAS INC

Locations

Alberta

Alberta Childrens Hospital
Calgary, Alberta, T3B 6A8

British Columbia

Child and Family Research Institute
Vancouver, British Columbia, V5Z 4H4

Ontario

Hospital For Sick Children
Toronto, Ontario, M5G 1X8

Results

See the results from the trial NCT04940624. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
Did you find what you were looking for?