Ignite Creation Date:
2024-05-05 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 9:15 AM
Study NCT ID:
NCT00158717
Status:
COMPLETED
Last Update Posted:
2014-01-07
First Post:
2005-09-07
Brief Title:
Observational Study of the Durability of Seroconversion Chronic HBV Patients Who Seroconverted in a Previous Gilead-Sponsored Study of ADV
Sponsor:
Gilead Sciences
Organization:
Gilead Sciences
Study Overview
Official Title:
A Phase 3b Long-Term Observational Study of the Durability of Seroconversion in Patients With Chronic Hepatitis B Virus Infection Who Have Seroconverted While Participating in a Previous Gilead-Sponsored Study of Adefovir Dipivoxil
Status:
COMPLETED
Status Verified Date:
2014-01
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 investigate the durability of HBeAg seroconversion in patients with chronic hepatitis B virus infection HBV who have seroconverted while participating in a previous Gilead-sponsored study of adefovir dipivoxil
Detailed Description:
The primary objective of this study is to investigate the durability of HBeAg seroconversion in patients with chronic hepatitis B virus infection HBV who have seroconverted while participating in a previous Gilead-sponsored study of adefovir dipivoxil
The secondary objective of this study is to investigate the durability of HBeAg loss in patients with chronic hepatitis B virus infection HBV who have experienced durable HBeAg loss while participating in a previous Gilead-sponsored study of adefovir dipivoxil
The secondary objective of this study is to investigate the durability of HBeAg loss in patients with chronic hepatitis B virus infection HBV who have experienced durable HBeAg loss while participating in a previous Gilead-sponsored study of adefovir dipivoxil
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