Clinical Trials Directory

Trials / Completed

CompletedNCT04792333

Pharmacokinetics in End Stage Renal Disease Patients

A Phase I Study to Compare Pharmacokinetic Parameters of Firibastat and Its Metabolites (EC33 and QGC515) in Healthy Subjects Versus End Stage Renal Disease (ESRD) Patients After a Single Oral Administration of Firibastat 500 mg

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
28 (actual)
Sponsor
Quantum Genomics SA · Industry
Sex
Male
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The study is a multicentre, open label, phase I, two arms study to compare pharmacokinetic of firibastat after a single oral dose of firibastat 500 mg in fourteen healthy male volunteers and in fourteen End Stage Renal Disease (ESRD) patients not yet in dialysis.

Detailed description

It is planned to enroll a total of 28 subjects to receive a single oral dose of investigational medicinal product (IMP): 14 ESRD patients will be enrolled in three Hungarian centres (1st arm) and 14 Healthy volunteers will be enrolled by Eurofins Optimed in Gières, France (2nd arm). Subjects will be screened for eligibility to participate in the study up to 21 days prior to the first administration. For both arm, subjects will be admitted into the Clinical Research Unit (CRU) on Day -3. On the morning of Day 1, subjects will receive a single 500 mg oral dose of firibastat following an overnight fast (i.e., at least 10 hours). Subjects will be confined to the CRU until discharge on Day 3 with PK blood sample draws for measurement of firibastat and its main metabolites being taken throughout the confinement. A follow-up post study visit will occur on Day 10 post-dose to ensure the ongoing wellbeing of the subjects.

Conditions

Interventions

TypeNameDescription
DRUGfiribastatSingle oral dose of 500 mg administration on Day 1

Timeline

Start date
2019-09-17
Primary completion
2020-07-10
Completion
2020-07-10
First posted
2021-03-10
Last updated
2021-03-10

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04792333. Inclusion in this directory is not an endorsement.