Back to results

Absorption, Distribution, Metabolism and Excretion of [14C]-Labelled BIA 3-202 and Metabolites

Primary Purpose

Parkinson's Disease

Status

Completed

Phase

Phase 1

Locations

Switzerland

Study Type

Interventional

Intervention

BIA 3-202 (200 mg)

About this trial

This is an interventional treatment trial for Parkinson's Disease focused on measuring Nebicapone, Parkinson's disease

Eligibility Criteria

40 Years - 55 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

Healthy male subject, 40-55 years of age. Take only Caucasians.
Clinically acceptable sitting blood pressure and pulse rate , i.e.: BP: 110-160 mmHg systolic, 65-95 mmHg diastolic and pulse rate: 50-100 bpm. Blood pressure and pulse will be measured after 3 minutes resting in a sitting position.
Subject body weight must be between 50 and 95 kg and within -10% / +20% of normal for their height and frame size (according to Metropolitan Life Insurance Table, see Appendix 1&2 of the Study Protocol). Frame size will be determined using elbow breadth measurement.
Normal 12-lead ECG.
Ability to communicate well with the investigator and comply with the requirements of the entire study.
The subject has given his written informed consent to participate in the study.

Exclusion Criteria:

History of serious adverse reactions or hypersensitivity to any drug.
Presence or history of allergies requiring acute or chronic treatment (except seasonal allergic rhinitis).
History of alcohol or drug abuse in the last 5 years.
Abnormal physical findings of clinical significance at the screening examination or baseline which would interfere with the objectives of the study.
Need of any prescription medication within 14 days prior to the administration of the drug and/or nonprescription medication within 7 days prior to the administration of the drug.
Participation in other clinical trials during the previous month in which an investigational drug or a commercially available drug was tested.
Loss of 500 mL blood or more during the 3 month period before the study, e.g., as a donor.
Existence of any surgical or medical condition which might interfere with the absorption, distribution, metabolism or excretion of the drug, i.e., impaired renal or hepatic function, diabetes mellitus, cardiovascular abnormalities, chronic symptoms of pronounced constipation or diarrhoea or conditions associated with total or partial obstruction of the urinary tract.
Symptoms of a significant somatic or mental illness in the 4 week period preceding drug administration.
History of hepatitis B and / or C and / or positive serology results which indicate the presence of hepatitis B and / or C.
Positive results from the HIV serology.
Clinically significant abnormal laboratory values (as determined by the Principal Investigator) at the screening evaluation, however, liver parameters (SGPT, SGOT) and CK values must be within the normal range.
Positive results of the drug screening.
Known hypersensitivity to BIA 3-202.
Heavy smokers, i.e., more than 10 cigarettes per day.
Exposure to artificial ionizing radiation in the last 12 months (e.g., x-ray investigation).
Subject who had more than 4 flights (with more than 2 hours flight time) within the last year prior to the administration of the drug.

Sites / Locations

Swiss Pharma Contract Ltd

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Nebicapone (200 mg)

Arm Description

Each subject was to receive one single dose of 2.5 MBq [14C]-labelled BIA 3-202 (200 mg) together with a total of 250 mL non-carbonated water. The study drug was given after an overnight fast of at least 10 hours after the in-house stay. During waking hours on Day 1, subjects had to have a fluid intake of at least 150 mL per hour starting 1 hour before study drug administration.

Outcomes

Primary Outcome Measures

maximum plasma concentration (Cmax)

time of occurrence of Cmax (tmax)

area under the plasma concentration-time curve from time zero to the last sampling time at which concentrations are at or above the limit of quantification, calculated by the linear trapezoidal rule (AUC0-t)

area under the plasma concentration versus time curve from time zero to infinity, calculated from AUC0-t + (C(t)/λz), where C(t) is the last quantifiable concentration and λz the apparent terminal rate constant (AUC0-∞)

Secondary Outcome Measures

Full Information

NCT ID

NCT02772614

First Posted

May 12, 2016

Last Updated

May 12, 2016

Sponsor

Bial - Portela C S.A.

1. Study Identification

Unique Protocol Identification Number

NCT02772614

Brief Title

Absorption, Distribution, Metabolism and Excretion of [14C]-Labelled BIA 3-202 and Metabolites

Official Title

An Open-label Study in Healthy Male Subjects to Assess the Absorption, Distribution, Metabolism and Excretion of [14C]-Labelled BIA 3-202 and Metabolites Following a Single-dose Oral Administration

Study Type

Interventional

2. Study Status

Record Verification Date

May 2016

Overall Recruitment Status

Completed

Study Start Date

January 2006 (undefined)

Primary Completion Date

February 2006 (Actual)

Study Completion Date

February 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Bial - Portela C S.A.

4. Oversight

Data Monitoring Committee

5. Study Description

Brief Summary

The purpose of this study is: To determine the rate and routes of excretion of BIA 3-202 and the mass balance in urine and faeces To determine the kinetics of total radioactivity in blood To determine the kinetics of total radioactivity in plasma To determine the kinetics of BIA 3-202 and its metabolites in plasma

Detailed Description

Monocentre, open, non-placebo-controlled, single-group, single-dose study. Safety measurements (12-lead ECG, vital signs, blood chemistry and haematology) were conducted before and after the study, adverse events were monitored throughout the study. Each subject was to receive a single oral dose of 2.5 MBq [14C]-labelled BIA 3-202 (200 mg). This was the intended radiolabelled dose without any losses; the actual administered dose was of 2.29 MBq [14C]-labelled BIA 3-202 (200 mg). Subjects were hospitalized the day before the administration until 264 hours thereafter. Whole blood samples (2 mL) for total radioactivity analysis, plasma samples (1.5 mL) for total radioactivity analysis, and plasma samples (7 mL) for analysis of BIA 3-202 and its metabolites were collected at the following times: pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 72, 120, 168, 216, and 264 hours post-dose. Urine was sampled before the drug administration (pre-dose), then it was collected from 0-4, 4-8, 8-24, 24-48, 48-72, 72-120, 120-168, 168-216, and 216-264 hours post-dose. Aliquots of each sample were taken for liquid scintillation counting by the investigator. Aliquots were separated for determination of parent drug and metabolite patterns. A baseline faeces sample was obtained during the screening or baseline period. Following dose, each faeces sample was collected in a separate container during the 264 hours post-dose period. Vomitus (if produced) was collected.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Parkinson's Disease

Keywords

Nebicapone, Parkinson's disease

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 1

Interventional Study Model

Single Group Assignment

Masking

None (Open Label)

Allocation

N/A

Enrollment

4 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Nebicapone (200 mg)

Arm Type

Experimental

Arm Description

Intervention Type

Drug

Intervention Name(s)

BIA 3-202 (200 mg)

Intervention Description

200 mg powder for oral use of unlabelled BIA 3-202

Primary Outcome Measure Information:

Title

maximum plasma concentration (Cmax)

Time Frame

pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 72, 120, 168, 216, and 264 hours post-dose

Title

time of occurrence of Cmax (tmax)

Time Frame

pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 72, 120, 168, 216, and 264 hours post-dose

Title

Time Frame

pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 72, 120, 168, 216, and 264 hours post-dose

Title

Time Frame

pre-dose and 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 36, 48, 72, 120, 168, 216, and 264 hours post-dose

10. Eligibility

Sex

Male

Minimum Age & Unit of Time

40 Years

Maximum Age & Unit of Time

55 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Healthy male subject, 40-55 years of age. Take only Caucasians. Clinically acceptable sitting blood pressure and pulse rate , i.e.: BP: 110-160 mmHg systolic, 65-95 mmHg diastolic and pulse rate: 50-100 bpm. Blood pressure and pulse will be measured after 3 minutes resting in a sitting position. Subject body weight must be between 50 and 95 kg and within -10% / +20% of normal for their height and frame size (according to Metropolitan Life Insurance Table, see Appendix 1&2 of the Study Protocol). Frame size will be determined using elbow breadth measurement. Normal 12-lead ECG. Ability to communicate well with the investigator and comply with the requirements of the entire study. The subject has given his written informed consent to participate in the study. Exclusion Criteria: History of serious adverse reactions or hypersensitivity to any drug. Presence or history of allergies requiring acute or chronic treatment (except seasonal allergic rhinitis). History of alcohol or drug abuse in the last 5 years. Abnormal physical findings of clinical significance at the screening examination or baseline which would interfere with the objectives of the study. Need of any prescription medication within 14 days prior to the administration of the drug and/or nonprescription medication within 7 days prior to the administration of the drug. Participation in other clinical trials during the previous month in which an investigational drug or a commercially available drug was tested. Loss of 500 mL blood or more during the 3 month period before the study, e.g., as a donor. Existence of any surgical or medical condition which might interfere with the absorption, distribution, metabolism or excretion of the drug, i.e., impaired renal or hepatic function, diabetes mellitus, cardiovascular abnormalities, chronic symptoms of pronounced constipation or diarrhoea or conditions associated with total or partial obstruction of the urinary tract. Symptoms of a significant somatic or mental illness in the 4 week period preceding drug administration. History of hepatitis B and / or C and / or positive serology results which indicate the presence of hepatitis B and / or C. Positive results from the HIV serology. Clinically significant abnormal laboratory values (as determined by the Principal Investigator) at the screening evaluation, however, liver parameters (SGPT, SGOT) and CK values must be within the normal range. Positive results of the drug screening. Known hypersensitivity to BIA 3-202. Heavy smokers, i.e., more than 10 cigarettes per day. Exposure to artificial ionizing radiation in the last 12 months (e.g., x-ray investigation). Subject who had more than 4 flights (with more than 2 hours flight time) within the last year prior to the administration of the drug.

Facility Information:

Facility Name

Swiss Pharma Contract Ltd

City

Allschwil

State/Province

Basel

ZIP/Postal Code

CH-4123

Country

Switzerland

12. IPD Sharing Statement

Plan to Share IPD

Learn more about this trial

Absorption, Distribution, Metabolism and Excretion of [14C]-Labelled BIA 3-202 and Metabolites

We'll reach out to this number within 24 hrs