Ignite Creation Date:
2024-05-05 @ 5:36 PM
Last Modification Date:
2024-10-26 @ 9:34 AM
Study NCT ID:
NCT00492427
Status:
COMPLETED
Last Update Posted:
2009-01-08
First Post:
2007-06-26
Brief Title:
Clinical Study of R744 to Predialysis Patients Phase III Comparative Study in Comparison With Epoetin Beta
Sponsor:
Chugai Pharmaceutical
Organization:
Chugai Pharmaceutical
Study Overview
Official Title:
Correction and Maintenance Study of Subcutaneous Injections of R744 to Predialysis Patients Phase III Comparative Study in Comparison With Epoetin Beta
Status:
COMPLETED
Status Verified Date:
2009-01
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 study used as the comparative drug epoetin beta will assess the efficacy and safety of subcutaneous R744 in renal anemia patients on Predialysis
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