Ignite Creation Date:
2024-05-05 @ 12:06 PM
Last Modification Date:
2024-10-26 @ 9:20 AM
Study NCT ID:
NCT00249860
Status:
COMPLETED
Last Update Posted:
2013-08-06
First Post:
2005-11-04
Brief Title:
A Multicenter Phase 3 Study of Interferon-beta-1a for the Treatment of Chronic Hepatitis C in Asian Subjects
Sponsor:
EMD Serono
Organization:
EMD Serono
Study Overview
Official Title:
A Multicentre Phase III Study of Interferon-beta-1a for the Treatment of Chronic Hepatitis C in Asian Subjects
Status:
COMPLETED
Status Verified Date:
2013-08
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:
The main objective of this study is to establish interferon-beta-1a as the treatment of choice for chronic Hepatitis C with better efficacy and safety profiles in monotherapy or combination therapy
This will be a multicenter randomized double-blind placebo-controlled study with a placebo to be crossed-over to a combination of interferon-beta-1a and ribavirin or no treatment during an open-label extension phase The duration of the trial will be 48 weeks with a double-blind period of 12 weeks
The study will recruit 257 eligible subjects of either sex It will be conducted by approximately 16 Investigators investigational centers in 3 countries China Hong Kong and Singapore
This will be a multicenter randomized double-blind placebo-controlled study with a placebo to be crossed-over to a combination of interferon-beta-1a and ribavirin or no treatment during an open-label extension phase The duration of the trial will be 48 weeks with a double-blind period of 12 weeks
The study will recruit 257 eligible subjects of either sex It will be conducted by approximately 16 Investigators investigational centers in 3 countries China Hong Kong and Singapore
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