Skip to main content
Clinical Trials/NCT01807000
NCT01807000
Completed
Phase 1

A Phase 1 Study to Investigate the Absorption, Metabolism, and Excretion of [14C] Prucalopride Succinate Following a Single Oral Dose in Healthy Male Subjects

Shire1 site in 1 country6 target enrollmentMarch 18, 2013

Overview

Phase
Phase 1
Intervention
Radiolabeled Prucalopride Succinate
Conditions
Healthy
Sponsor
Shire
Enrollment
6
Locations
1
Primary Endpoint
Total Body Clearance (CL/F) of Radiolabelled Prucalopride Succinate
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Phase I study to evaluate the excretion of radioactivity, the metabolic profile, pharmacokinetics, safety and tolerability following a single oral administration of [14C] Prucalopride Succinate in healthy male volunteers aged 18 to 50 years (inclusive).The purpose of this study is to investigate how and how quickly Prucalopride Succinate or its break down products are excreted by analysing blood, faeces and urine samples collected during the study.

Registry
clinicaltrials.gov
Start Date
March 18, 2013
End Date
April 28, 2013
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
Shire
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Males aged between 18 and 50 years, inclusive
  • Body mass index (BMI) of ≥18 and ≤30 kg/m2
  • No more than 2 bowel movements per day or fewer than 3 bowel movement per week
  • Provision of signed and dated, written informed consent prior to any study specific procedures

Exclusion Criteria

  • Have participated in a \[14C\]-study within the last 6 months.
  • Exposure to clinically significant radiation within 12 months prior to dose (for example, serial X-ray or computed tomography scans, barium meal, current employment in a job requiring radiation exposure monitoring).
  • Male subjects who consume more than 21 units of alcohol per week or 3 units per day.

Arms & Interventions

Radiolabeled Prucalopride Succinate

Intervention: Radiolabeled Prucalopride Succinate

Outcomes

Primary Outcomes

Total Body Clearance (CL/F) of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

The rate at which a drug is removed from the body.

Area Under the Plasma Concentration Versus Time Curve From Time Zero to Infinity (AUC 0→∞) of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

AUC can be used as a measure of drug exposure. It is derived from drug concentration and time so it gives a measure how much and how long a drug stays in a body.

Time to Maximum Plasma Concentration (Tmax) of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Tmax is the time after administration of a drug when the maximum plasma concentration in the body is reached.

Plasma Half-Life (T1/2) of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

The time it takes for the blood plasma concentration of a substance to halve.

Volume of Distribution (Vz/F) of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

The distribution of a medication between plasma and the rest of the body.

AUC 0→∞ Whole Blood Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Cmax Whole Blood Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Maximum Plasma Concentration (Cmax) of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Cmax is a term that refers to the maximum (or peak) concentration that a drug achieves in the body after the drug has been administered.

Tmax Whole Blood Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Half-Life Whole Blood Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

AUC 0→∞ Plasma Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Cmax Plasma Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Tmax Plasma Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Half-Life Plasma Total Radioactivity of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Percent Total Radioactivity Excreted in Urine of Radiolabelled Prucalopride Succinate

Time Frame: 240 hours post-dose

Percent Total Radioactivity Excreted in Stool of Radiolabelled Prucalopride Succinate

Time Frame: Over 240 hours post-dose

Study Sites (1)

Loading locations...

Similar Trials