RecruitingPhase 2NCT04580420
Safety & Efficacy of DCR-PHXC in Patients With PH1 and ESRD
Studying Primary hyperoxaluria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Dicerna Pharmaceuticals, Inc., a Novo Nordisk company
- Principal Investigator
- Clinical Transparency (dept. 2834)Novo Nordisk A/S
- Intervention
- DCR-PHXC(drug)
- Enrollment
- 28 enrolled
- Eligibility
- All sexes
- Timeline
- 2021 – 2032
Study locations (16)
- Clinical Trial Site, San Francisco, California, United States
- Clinical Trial Site, Boston, Massachusetts, United States
- Clinical Trial Site, Rochester, Minnesota, United States
- Clinical Trial Site, New York, New York, United States
- Clinical Trial Site, Bron, France
- Clinical Trial Site, Paris, France
- Clinical Trial Site, Bonn, Germany
- Clinical Trial Site, Heidelberg, Germany
- Clinical Trial Site, Roma, Italy
- Clinical Trial Site, Beirut, Lebanon
- Clinical Trial Site, Casablanca, Morocco
- Clinical Trial Site, Oradea, Romania
- Clinical Trial Site, Barcelona, Spain
- Clinical Trial Site, Santa Cruz de Tenerife, Spain
- Clinical Trial Site, Dubai, United Arab Emirates
- +1 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.
Open NCT04580420 on ClinicalTrials.govOther trials for Primary hyperoxaluria
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