BONAPH1DE, A Prospective Observational Study of Patients With Primary Hyperoxaluria Type 1 (PH1)
About the study
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.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
* Documented diagnosis of PH1, per physician's determination
EXCLUSION CRITERIA
Exclusion Criteria:
* Currently enrolled in a clinical trial for any investigational agent
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study Details
Contition
Primary Hyperoxaluria Type 1
Participants Needed
200
Est. Completion Date
Sep 1, 2028
Treatment Type
OBSERVATIONAL
Sponsor
Alnylam Pharmaceuticals
ClinicalTrials.gov NCT Identifier
NCT04982393
Study Number
ALN-GO1-007
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