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Primary Hyperoxaluria clinical trials

View clinical trials related to Primary Hyperoxaluria.

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NCT ID: NCT03819647 Completed - Clinical trials for Primary Hyperoxaluria

Evaluation of the Efficacy of Stiripentol (Diacomit) as Monotherapy for the Treatment of Primary Hyperoxaluria

Start date: May 21, 2019
Phase: Phase 2
Study type: Interventional

Evaluation of the efficacy of stiripentol (Diacomit) as monotherapy for the treatment of primary hyperoxaluria. Pilot clinical study, open, prospective and multicenter.

NCT ID: NCT03392896 Completed - Clinical trials for Primary Hyperoxaluria

Study of DCR-PHXC-101 in Normal Healthy Volunteers and Patients With Primary Hyperoxaluria

Start date: December 6, 2017
Phase: Phase 1
Study type: Interventional

This is a double-blind, placebo-controlled, dose escalation trial of DCR-PHXC in Healthy Volunteers (HVs) and patients with Primary Hyperoxaluria (PH). Once safety has been established in HV, PH patients with a confirmed diagnosis of PH1 and PH2 will be enrolled across multiple dosing cohorts. The study design will allow enrollment of PH patient cohorts at a given dose level once safety has been demonstrated in HV at that dose level. The study will be conducted in two parts: Part A: Single ascending dose (SAD) in HV; Part B: SAD in patients with PH1 and PH2 (lagging Part A by 1 dose level cohort).

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: 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.