Clinical Trials List
2024-03-01 - 2030-03-31
Others
Recruiting6
ICD-10B18.1
Chronic viral hepatitis B without delta-agent
ICD-9070.32
Viral hepatitis B without mention of hepatic coma, chronic, without mention of hepatitis delta
A Long-Term Follow-up Study for Subjects with Chronic Hepatitis B Previously Treated with Imdusiran (AB-729)
-
Trial Applicant
-
Sponsor
NOVOTECH CLINICAL RESEARCH TAIWAN PTY LTD.
-
Trial scale
Multi-Regional Multi-Center
-
Update
2026/02/01
Investigators and Locations
Co-Principal Investigator
- 許銘澤 Digestive System Department
The Actual Total Number of Participants Enrolled
0 Recruiting
Co-Principal Investigator
- 許耀峻 Digestive System Department
The Actual Total Number of Participants Enrolled
0 Recruiting
Co-Principal Investigator
- Yi-Cheng Chen Digestive System Department
- Chau-Ting Yeh Digestive System Department
- Chen-Chun Lin Digestive System Department
The Actual Total Number of Participants Enrolled
0 Recruiting
The Actual Total Number of Participants Enrolled
0 Recruiting
Co-Principal Investigator
- Chia-Yen Dai Digestive System Department
- Jee-Fu Huang
- Ming-Lung Yu Digestive System Department
- Chung-Feng Huang
- 梁博程 Digestive System Department
- Ming-Lun Yeh Digestive System Department
The Actual Total Number of Participants Enrolled
0 Recruiting
The Actual Total Number of Participants Enrolled
0 Recruiting
Condition/Disease
Objectives
Test Drug
Active Ingredient
Dosage Form
Dosage
Endpoints
• Proportion and duration of participants who remain off nucleos(t)ide analogue (NA) therapy, as applicable.
• Proportion of participants who restart NA therapy, as applicable.
Inclution Criteria
The participant must:
a. Have previously participated in an imdusiran clinical trial,
b. Have discontinued nucleos(t)ide analogue (NA) therapy in that study,
c. Remain off NA therapy, and
d. Have completed less than 3 years of follow-up visits after NA discontinuation in the parent study.
Be able to review and provide written informed consent, including agreement to comply with all study visit schedules and protocol requirements.
Exclusion Criteria
The Estimated Number of Participants
-
Taiwan
16 participants
-
Global
35 participants