A Study to Assess Plasma Ammonia Time-Normalized Area Under the Curve and Rate of Ureagenesis in Healthy Adult Subjects

NCT04269122 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2020-03-30

No results posted yet for this study

Summary

The objective of the study is to characterize 24-hour plasma ammonia levels, characterize urea production rates in healthy normal subjects.

Conditions

  • Ornithine Transcarbamylase Deficiency

Interventions

OTHER

No Intervention

No intervention

Sponsors & Collaborators

Principal Investigators

  • Medical Director · Ultragenyx Pharmaceutical

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-02
Primary Completion
2020-02-20
Completion
2020-02-20
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04269122 on ClinicalTrials.gov