Viewing Study NCT00354094



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Last Modification Date: 2024-10-26 @ 9:26 AM
Study NCT ID: NCT00354094
Status: TERMINATED
Last Update Posted: 2007-11-08
First Post: 2006-07-18

Brief Title: SS-Reboxetine Long Term Safety Study In Post-Shingles Pain
Sponsor: Pfizer
Organization: Pfizer

Study Overview

Official Title: A Phase 2B Long-Term Randomized Open-Label Safety And Tolerability Trial Comparing SS-Reboxetine PNU-165442g With Routine Care In Patients With Postherpetic Neuralgia PHN
Status: TERMINATED
Status Verified Date: 2007-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: The study was stopped due to businessoperational issues
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess the long term up to 2 years safety and tolerability of SS-Reboxetine in patients with pain after shingles
Detailed Description: None

Study Oversight

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