Clinical Trials Directory

Trials / Completed

CompletedNCT03819647

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

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Biocodex · Industry
Sex
All
Age
6 Months
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGstiripentol (Diacomit)Administration of stiripentol per os

Timeline

Start date
2019-05-21
Primary completion
2020-12-18
Completion
2021-03-08
First posted
2019-01-28
Last updated
2021-03-26

Locations

3 sites across 1 country: France

Source: ClinicalTrials.gov record NCT03819647. Inclusion in this directory is not an endorsement.

Evaluation of the Efficacy of Stiripentol (Diacomit) as Monotherapy for the Treatment of Primary Hyperoxaluria (NCT03819647) · Clinical Trials Directory