Viewing Study NCT02214160



Ignite Creation Date: 2024-05-06 @ 3:08 AM
Last Modification Date: 2024-10-26 @ 11:29 AM
Study NCT ID: NCT02214160
Status: COMPLETED
Last Update Posted: 2023-08-01
First Post: 2014-08-06

Brief Title: Long-Chain Fatty Acid Oxidation Disorders LC-FAOD Extension Study for Subjects Previously Enrolled in Triheptanoin Studies
Sponsor: Ultragenyx Pharmaceutical Inc
Organization: Ultragenyx Pharmaceutical Inc

Study Overview

Official Title: An Open-label Long-Term Safety and Efficacy Extension Study in Subjects With Long-Chain Fatty Acid Oxidation Disorders LC-FAOD Previously Enrolled in UX007 or Triheptanoin Studies
Status: COMPLETED
Status Verified Date: 2023-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: True
If Expanded Access, NCT#: NCT03773770
Has Expanded Access, NCT# Status: AVAILABLE
Acronym: None
Brief Summary: The primary objective of this study is to evaluate the long-term safety and efficacy of UX007 in participants with LC-FAOD The secondary objectives of this study are to evaluate the effect of UX007 on energy metabolism in LC-FAOD and evaluate the impact of UX007 on clinical events associated with LC-FAOD
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?: None
Secondary IDs
Secondary ID Type Domain Link
2016-000322-19 EUDRACT_NUMBER None None