Viewing Study NCT00367692



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Last Modification Date: 2024-10-26 @ 9:27 AM
Study NCT ID: NCT00367692
Status: TERMINATED
Last Update Posted: 2009-09-09
First Post: 2006-08-21

Brief Title: Study Evaluating PSI-697 in Patients With Scleritis
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

Official Title: An Exploratory Double Blind Placebo-controlled Randomized Single-dose Cross-over Proof of Mechanism Study of Orally Administered PSI-697 in Patients With Scleritis
Status: TERMINATED
Status Verified Date: 2009-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To evaluate the safety of an orally administered single dose of PSI-697 in subjects with scleritis as a model of inflammatory disease To evaluate by in vivo confocal microscopy IVCM the effect of a single dose of PSI-697 on leukocyte rolling in the scleral blood vessels of subjects with scleritis
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