Viewing Study NCT05655520


Ignite Creation Date: 2025-12-25 @ 4:27 AM
Ignite Modification Date: 2025-12-26 @ 3:30 AM
Study NCT ID: NCT05655520
Status: TERMINATED
Last Update Posted: 2025-12-17
First Post: 2022-12-09
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: A Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Huntington's Disease
Sponsor: Supernus Pharmaceuticals, Inc.
Organization:

Study Overview

Official Title: A Phase 3, Multicenter, Open-label Safety Study to Evaluate the Long-term Safety and Tolerability of SAGE-718 in Participants With Huntington's Disease
Status: TERMINATED
Status Verified Date: 2025-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Internal company decision
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The primary purpose of the study is to evaluate the safety and tolerability of SAGE-718 softgel lipid capsule in participants with Huntington's Disease (HD)
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: