Viewing Study NCT00663702


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Study NCT ID: NCT00663702
Status: COMPLETED
Last Update Posted: 2015-03-09
First Post: 2008-04-18
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: Phase IIIB Switching From Intravenous to Subcutaneous Study
Sponsor: Bristol-Myers Squibb
Organization:

Study Overview

Official Title: A Phase 3B Multi-center Open-Label Study to Evaluate the Safety of Abatacept in Subjects Who Switch From Intravenous to Subcutaneous Abatacept Therapy
Status: COMPLETED
Status Verified Date: 2015-02
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: The purpose of this study is to determine whether switching to subcutaneous administration of abatacept will be safe in participants with rheumatoid arthritis who previously received long-term therapy with intravenous abatacept
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?: