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NCT06277037Recruiting

Long-Term Follow-up Study for Subjects With CHB Previously Treated With Imdusiran (AB729)

A Long-Term Follow-up Study for Subjects With Chronic Hepatitis B Previously Treated With Imdusiran (AB-729)

Source: ClinicalTrials.gov · Last updated 27 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a long term follow-up study for chronic hepatitis B (CHB) subjects who have received imdusiran treatment in a prior clinical trial, stopped NA therapy during that trial, and remain off therapy. Subjects may enroll after completing the end of study visit (baseline visit within 12 weeks ± 1 week from the end of study \[EOS\] visit) from their imdusiran clinical trial (the "parent study"). No interventions will be performed in this study other than blood sample collections, review of current medications, and reporting of any adverse events related to study procedures or NA therapy if restarted. Study participation will be for approximately 2 years (to complete a total of at least 3 years of follow-up while off NA therapy, inclusive of parent study participation).

Status (registry)
Recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
14 Feb 2024
Start date
11 Jul 2024
Primary completion date
30 Aug 2029
Lead sponsor
Arbutus Biopharma Corporation
Diseases
Hepatitis B
NCT number
NCT06277037

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 11 Jul 2024 to the primary completion date, 30 Aug 2029
  • 18 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Not applicable

Who the study is looking for

  • Have participated in a prior imdusiran clinical trial,
  • Have discontinued NA therapy in that trial and remain off NA therapy,
  • Have completed less than 3 years of follow-up visits after NA discontinuation in the parent study.
  • Have the ability to review and provide signed informed consent which includes compliance with all protocol-specified visit schedules and requirements.

Age in the registry: 20 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (18)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Alfred Hospital
Coordinator of this site? Confirm its status
MelbourneAustraliaRecruiting
Fiona Stanley Hospital
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MurdochAustraliaNot yet recruiting
University Hospital of Wales, Cardiff
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CardiffUnited KingdomNot yet recruiting
King's College Hospital
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LondonUnited KingdomNot yet recruiting
Royal London Hospital
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LondonUnited KingdomNot yet recruiting
Queen Mary Hospital
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Hong KongHong Kong SAR ChinaRecruiting
Prince of Wales Hospital
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ShatinHong Kong SAR ChinaRecruiting
Asan Medial Center
Coordinator of this site? Confirm its status
SeoulSouth KoreaNot yet recruiting
Arensia Exploratory Medicine Moldova
Coordinator of this site? Confirm its status
ChisinauMoldovaRecruiting
Changhua Christian Hospital
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ChanghuaTaiwanRecruiting
Chia-Yi Christian Hospital
Coordinator of this site? Confirm its status
Chiayi CityTaiwanRecruiting
E-DA Hospital
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Kaohsiung CityTaiwanRecruiting
Kaohsiung Medical University Chung-Ho Memorial Hospital
Coordinator of this site? Confirm its status
Kaohsiung CityTaiwanRecruiting
Taichung Veterans General Hospital
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TaichungTaiwanRecruiting
Chang Gung Medical Foundation - Linkou
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TaoyuanTaiwanRecruiting
Infectious Disease Care
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HillsboroughUnited StatesRecruiting
University of Miami Miller School of Medicine
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MiamiUnited StatesNot yet recruiting
Research and Education, Inc.
Coordinator of this site? Confirm its status
San DiegoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.