Evaluation of the Efficacy of Stiripentol (Diacomit) as Monotherapy for

See also
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Recruiting	`NCT05843851` - Genetic Newborn Screening for Cystinosis and Primary Hyperoxaluria	N/A
Recruiting	`NCT00588562` - Rare Kidney Stone Consortium Patient Registry
Completed	`NCT03391804` - Study of ALLN-177 in Patients Aged 12 Years or Older With Enteric or Primary Hyperoxaluria and Hyperoxalemia	Phase 2
Completed	`NCT03116685` - A Study to Evaluate the Efficacy and Safety of Oxabact in Patients With Primary Hyperoxaluria	Phase 3
Recruiting	`NCT05107830` - Phenotyping of Primary Hyperoxaluria
Active, not recruiting	`NCT04152200` - A Study to Evaluate Lumasiran in Patients With Advanced Primary Hyperoxaluria Type 1	Phase 3
Recruiting	`NCT05001269` - Nedosiran in Pediatric Patients From Birth to 11 Years of Age With PH and Relatively Intact Renal Function	Phase 2
Completed	`NCT03392896` - Study of DCR-PHXC-101 in Normal Healthy Volunteers and Patients With Primary Hyperoxaluria	Phase 1
Completed	`NCT02012985` - Study to Evaluate the Efficacy and Safety of Oxabact (OC5) in Patients With Primary Hyperoxaluria	Phase 1/Phase 2
Completed	`NCT01037231` - Phase 2/3 Oxabact Study	Phase 2/Phase 3
Completed	`NCT00589225` - Primary Hyperoxaluria Mutation Genotyping	Phase 1
Completed	`NCT02124395` - Health-related Quality of Life in Rare Kidney Stone
Completed	`NCT03350451` - An Extension Study of an Investigational Drug, Lumasiran (ALN-GO1), in Participants With Primary Hyperoxaluria Type 1	Phase 2

NCT number	NCT03819647
Study type	Interventional
Source	Biocodex
Contact
Status	Completed
Phase	Phase 2
Start date	May 21, 2019
Completion date	March 8, 2021

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

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms