BONAPH1DE, A Prospective Observational Study of Patients With Primary Hyperoxaluria Type 1 (PH1)
NCT04982393 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 207
Last updated 2026-04-24
Summary
The purpose of this study is to describe the natural history and progression of patients diagnosed with PH1, and to characterize the long-term real-world safety and effectiveness of lumasiran.
Conditions
- Primary Hyperoxaluria Type 1
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Medical Director · Alnylam Pharmaceuticals
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-12-13
- Primary Completion
- 2028-09-01
- Completion
- 2028-09-01
Countries
- United States
- Belgium
- Canada
- France
- Germany
- Israel
- Italy
- Netherlands
- Spain
- Switzerland
- United Kingdom
Study Locations
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