Viewing Study NCT01371435


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Study NCT ID: NCT01371435
Status: COMPLETED
Last Update Posted: 2017-06-08
First Post: 2011-06-09
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Drug Use Investigation for PAXIL Tablet
Sponsor: GlaxoSmithKline
Organization:

Study Overview

Official Title: Drug Use Investigation for PAXIL Tablet
Status: COMPLETED
Status Verified Date: 2017-05
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 post-marketing surveillance study is designed to detect adverse events (particularly clinically significant adverse drug reactions) occurring in clinical settings and to examine factors likely to affect the safety and efficacy of paroxetine.
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?: