Viewing Study NCT05338606


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Ignite Modification Date: 2025-12-26 @ 5:17 PM
Study NCT ID: NCT05338606
Status: NO_LONGER_AVAILABLE
Last Update Posted: 2025-02-10
First Post: 2022-04-13
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Expanded Access to Bimatoprost (Durysta)
Sponsor: AbbVie
Organization:

Study Overview

Official Title: Expanded Access to Bimatoprost
Status: NO_LONGER_AVAILABLE
Status Verified Date: 2025-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to Durysta (Bimatoprost) prior to approval by the local regulatory agency. Availability will depend on territory eligibility. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: