Viewing Study NCT00266695



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Last Modification Date: 2024-10-26 @ 9:21 AM
Study NCT ID: NCT00266695
Status: COMPLETED
Last Update Posted: 2016-10-06
First Post: 2005-12-15

Brief Title: Treatment for Completers of the Study B7A-MC-MBCM
Sponsor: Chromaderm Inc
Organization: Chromaderm Inc

Study Overview

Official Title: Open-Label Treatment for Patients Completing Study B7A-MC-MBCM
Status: COMPLETED
Status Verified Date: 2016-08
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: To provide ruboxistaurin treatment to patients who completed the B7A-MC-MBCM study NCT00604383 and who are felt by the investigator to have the potential to benefit from the ruboxistaurin treatment Patients must be off study drug for 6 to 18 months from completion of B7A-MC-MBCM before beginning B7A-MC-MBDV Additional data will be gathered to determine the long-term safety and effect of ruboxistaurin on vision
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
Secondary IDs
Secondary ID Type Domain Link
B7A-MC-MBDV OTHER Eli Lilly and Company None