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Primary Hyperoxaluria clinical trials

View clinical trials related to Primary Hyperoxaluria.

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NCT ID: NCT03391804 Completed - Clinical trials for Primary Hyperoxaluria

Study of ALLN-177 in Patients Aged 12 Years or Older With Enteric or Primary Hyperoxaluria and Hyperoxalemia

Start date: July 17, 2018
Phase: Phase 2
Study type: Interventional

Evaluate the efficacy and safety of ALLN-177 in reducing plasma and urinary oxalate levels in adult and pediatric patients with enteric hyperoxaluria and hyperoxalemia or primary hyperoxaluria

NCT ID: NCT03350451 Completed - Clinical trials for Primary Hyperoxaluria

An Extension Study of an Investigational Drug, Lumasiran (ALN-GO1), in Participants With Primary Hyperoxaluria Type 1

Start date: April 4, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the long-term safety and tolerability of lumasiran in participants with Primary Hyperoxaluria Type 1.

NCT ID: NCT03116685 Completed - Clinical trials for Primary Hyperoxaluria

A Study to Evaluate the Efficacy and Safety of Oxabact in Patients With Primary Hyperoxaluria

Start date: January 9, 2018
Phase: Phase 3
Study type: Interventional

This study will evaluate the efficacy and safety of OC5 in patients with PH.

NCT ID: NCT02340689 Completed - Clinical trials for Primary Hyperoxaluria

Primary Hyperoxaluria Mutation Genotyping/Phenotyping

Start date: October 2013
Phase:
Study type: Observational

Specific mutations relating to hyperoxaluria will be determined via DNA analysis by the Mayo RKSC research staff.

NCT ID: NCT02124395 Completed - Clinical trials for Primary Hyperoxaluria

Health-related Quality of Life in Rare Kidney Stone

Start date: August 2013
Phase:
Study type: Observational [Patient Registry]

Assessment of Health-related Quality of Life in Rare Kidney Stone Formers in the Rare Kidney Stone Consortium

NCT ID: NCT02026388 Recruiting - Clinical trials for Primary Hyperoxaluria

Rare Kidney Stone Consortium Biobank

Start date: May 2013
Phase:
Study type: Observational

This study is being done to obtain samples from patients with primary hyperoxaluria, cystinuria, adenine phosphoribosyl transferase (APRT) deficiency, and Dent disease, and from their family members, for use in future research.

NCT ID: NCT02012985 Completed - Clinical trials for Primary Hyperoxaluria

Study to Evaluate the Efficacy and Safety of Oxabact (OC5) in Patients With Primary Hyperoxaluria

Start date: December 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if Oxalobacter formigenes is effective at lowering urinary oxalate levels in patients with primary hyperoxaluria.

NCT ID: NCT02000219 Completed - Clinical trials for Primary Hyperoxaluria

Study to Evaluate the Efficacy and Safety of Oxabact (OC5) in Primary Hyperoxaluria Patients Who Are on Dialysis

Start date: May 19, 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if Oxalobacter formigenes is effective at lowering plasma oxalate levels in patients with primary hyperoxaluria who are on dialysis.

NCT ID: NCT01037231 Completed - Clinical trials for Primary Hyperoxaluria

Phase 2/3 Oxabact Study

Start date: December 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine if Oxalobacter formigenes is effective at lowering urinary oxalate levels in patients with primary hyperoxaluria.

NCT ID: NCT00875823 Withdrawn - Kidney Stones Clinical Trials

International Registry for Primary Hyperoxaluria

Start date: September 2003
Phase: N/A
Study type: Observational

The purpose of this study is to collect medical information from a large number of patients in many areas of the world with primary hyperoxaluria. This medical information will be entered into a registry to help the investigators compare similarities and differences in patients and their symptoms. The more patients that the investigators are able to enter into the registry, the more the investigators will be able to understand primary hyperoxaluria and learn better ways of treating patients with this disease. It is the investigators hope that by entering as many patients with PH as possible, the information that the investigators collect may help physicians diagnose patients sooner and determine what treatments may work best on patients with similar medical or genetic backgrounds.