Clinical Trials Directory

Trials / Completed

CompletedNCT02110147

Open-Label Study of Uridine Triacetate in Pediatric Patients With Hereditary Orotic Aciduria

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
4 (actual)
Sponsor
Wellstat Therapeutics · Industry
Sex
All
Age
6 Months – 19 Years
Healthy volunteers
Not accepted

Summary

This protocol has two parts - the Main Study which is 42 days in length and the Treatment Extension which allows the patients who complete the Main Study to continue receiving treatment with uridine triacetate. The purpose of this study is to replace oral administration of uridine with oral administration of uridine triacetate in patients with hereditary orotic aciduria who have received (or would reasonably be expected to receive) clinical benefit from treatment with exogenous uridine. It is also to document the continued clinical benefit of exogenous uridine when patients are switched from oral administration of uridine to oral administration of uridine triacetate.

Detailed description

Data to be collected during the Main Study include demographic, baseline disease information and medical history including all prior disease-directed therapy. In addition, vital signs, laboratory values and adverse events information will be collected and recorded. Urine samples will be obtained and measured for orotic acid and orotidine levels. Systemic levels of uridine will be evaluated from plasma samples collected at set timepoints. Upon successful completion of the Main Study and entry into the Treatment Extension, physical exams and vital signs will be performed every six (6) months. Additionally, plasma samples to measure systemic levels of uridine and urine samples to measure levels of orotic acid and orotidine will be collected every (6) six months.

Conditions

Interventions

TypeNameDescription
DRUGuridine triacetate

Timeline

Start date
2014-04-01
Primary completion
2014-12-01
Completion
2016-09-08
First posted
2014-04-10
Last updated
2017-07-31
Results posted
2017-06-28

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02110147. Inclusion in this directory is not an endorsement.