Active, not recruitingPhase 3NCT06903338
A Study to Evaluate Tobevibart + Elebsiran in Chronic HDV Infection
Studying Hepatitis delta
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Vir Biotechnology, Inc.
- Intervention
- Tobevibart(drug)
- Enrollment
- 124 target
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2025 – 2031
Study locations (30)
- Investigative Site, Chandler, Arizona, United States
- Investigative Site, Los Angeles, California, United States
- Investigative Site, Redwood City, California, United States
- Investigative Site, San Francisco, California, United States
- Investigative Site, DeLand, Florida, United States
- Investigative Site, Chicago, Illinois, United States
- Investigative Site, Baltimore, Maryland, United States
- Investigative Site, Hillsborough, New Jersey, United States
- Investigative Site, New York, New York, United States
- Investigative Site, Murray, Utah, United States
- Investigative Site, Seattle, Washington, United States
- Investigative Site, Calgary, Alberta, Canada
- Investigative Site, Montreal, Quebec, Canada
- Investigative Site, Montreal, Canada
- Investigative Site, Ottawa, Canada
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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