Clinical Trials Directory

Trials / Completed

CompletedNCT02092168

Pharmacokinetics of BIA 9-1067 and Its Metabolites in Healthy Male Elderly Subjects and in Healthy Male Young Subjects

Single-dose and Steady-state Pharmacokinetics of BIA 9-1067 and Its Metabolites in Healthy Male Elderly Subjects Compared With Those in Healthy Male Young Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Bial - Portela C S.A. · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the effects of age on the pharmacokinetic (PK) profile of BIA 9-1067 and its metabolites.

Detailed description

Methodology: Single-centre, open-label, parallel group, non-randomised multiple-dose 7-day study in 12 healthy elderly and 12 healthy younger male subjects. Duration of treatment: Each subject participated in the study for approximately 6 weeks. Participation included a screening evaluation within 28 days before inpatient period, a 12 day inpatient period and an end of study visit (ESV) 7 to 10 days after the discharge from the Unit. The study design followed the recommendations of the CPMP/ICH/379/95 (ICH Topic E7) Note for Guidance on Studies in Support of Special Populations: Geriatrics, namely in the inclusion of subjects aged 65 years or older and contemplating single-dose and steady-state PK profiles. As the primary endpoint of the study was to characterize the pharmacokinetic profile of BIA 9-1067 and its metabolites in different parallel groups, there was no need to implement blinding procedures or to include a control group. Consequently, the trial was an open label study. Healthy subjects rather than patients with Parkinson's disease have been chosen as the study population, due to the lack of over-toxicity of the drug and an acceptable risk-benefit ratio. This allowed for a better interpretation of the study results, as there were no confounding factors resulting from changes in disease state and or concomitant medications. The subjects were given a screening number after signing the informed consent by chronological order of inclusion in each group (young/elderly).

Conditions

Interventions

TypeNameDescription
DRUGBIA 9-1067

Timeline

Start date
2008-10-01
Primary completion
2009-01-01
Completion
2009-01-01
First posted
2014-03-20
Last updated
2015-01-14
Results posted
2015-01-14

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02092168. Inclusion in this directory is not an endorsement.