RecruitingPHASE1, PHASE2NCT06839235
Phase 1/2 Study of ABO-101 in Primary Hyperoxaluria Type 1 (redePHine)
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
- Arbor Biotechnologies
- Principal Investigator
- Winston Yan, MD, PhDArbor Biotechnologies
- Intervention
- ABO-101(drug)
- Enrollment
- 23 enrolled
- Eligibility
- 6-64 years · All sexes
- Timeline
- 2025 – 2043
Study locations (7)
- Mayo Clinic, Rochester, Minnesota, United States
- Nucleus Network, Saint Paul, Minnesota, United States
- Hospices Civils de Lyon- Hôpital Femmes Mères Enfants, Lyon, France
- Kindernierenzentrum Bonn, Bonn, Germany
- Heidi Chaker, Sfax, Tunisia
- Queen Elizabeth Hospital Birmingham, Birmingham, United Kingdom
- Royal Free Hospital, London, United Kingdom
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 NCT06839235 on ClinicalTrials.govOther trials for Primary hyperoxaluria
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- RECRUITINGEARLY PHASE1NCT06511349Clinical Exploration Study of YOLT-203 in the Treatment of Type 1 Primary Hyperoxaluria (PH1)RenJi Hospital
- RECRUITINGNCT06225882Retrospective and Prospective Follow-up of Patients With Primary Hyperoxaluria Type 1 Treated With Lumasiran in France.Hospices Civils de Lyon
- ACTIVE NOT RECRUITINGNCT04982393BONAPH1DE, A Prospective Observational Study of Patients With Primary Hyperoxaluria Type 1 (PH1)Alnylam Pharmaceuticals
- RECRUITINGPHASE2NCT04580420Safety & Efficacy of DCR-PHXC in Patients With PH1 and ESRDDicerna Pharmaceuticals, Inc., a Novo Nordisk company