CompletedPhase 3NCT03116685
A Study to Evaluate the Efficacy and Safety of Oxabact in Patients With Primary Hyperoxaluria
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
- OxThera
- Principal Investigator
- Gesa Schalk, MD, M.DKindernierenZentrum, Bonn, Germany
- Intervention
- Oxabact OC5 - Oxalobacter formigenes HC-1(biological)
- Enrollment
- 25 enrolled
- Eligibility
- 2 years · All sexes
- Timeline
- 2018 – 2021
Study locations (10)
- Vanderbilt University Hospital, Nashville, Tennessee, United States
- Centre Hospitalier Universitaire de Liège, Liège, Belgium
- Hôpital Robert Debré, Paris, France
- Kindernierenzentrum Bonn, Bonn, Germany
- Hospital Vall d' Hebron, Barcelona, Spain
- Hédi Chaker University Hospital, Sfax, Tunisia
- Sahloul University Hospital, Sousse, Tunisia
- Charles Nicolle University Hospital, Tunis, Tunisia
- Royal Free Hospital, London, United Kingdom
- Nottingham Children's Hospital, Nottingham, 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 NCT03116685 on ClinicalTrials.govOther trials for Primary hyperoxaluria
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