An Open-label Study in Healthy Male Subjects to Assess the Absorption, Distribution, Metabolism and Excretion of [14C]-Labelled BIA 9-1067 and Metabolites

NCT ID: NCT02169427

Last Updated: 2015-08-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-03-31
• Study Completion Date: 2011-07-31

Brief Summary

The purpose of this study is to determine the rate and routes of excretion of OPC and the mass balance in urine, faeces and expired air.

Detailed Description

This was a single-centre, open-label ADME study in 6 healthy male subjects. Subjects received a single dose of 100 mg OPC, containing 3.39 MBq of [14C] OPC as oral capsules.

The study consisted of an eligibility screening period within 3 weeks prior to drug administration, admission on Day -1, a treatment period involving drug administration on Day 1 followed by matrix collections for PK purposes and safety evaluations up to Day 11, discharge on Day 11, six 24-hour hospitalizations on Days 14/15, 21/22 (+/ 1 day), 28/29 (+/- 1 day), 42/43 (+/- 2 days), 56/57 (+/- 2 days) and 77/78 (+/ 3 days) for PK sample collections, and a follow up visit performed at least 14 days after discharge from the last 24-hour hospitalization or at early discontinuation.

Conditions

Parkinson's Disease (PD)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Opicapone (OPC)

100 mg OPC

Group Type: EXPERIMENTAL

OPC

Intervention Type: DRUG

The drug substance of 100 mg OPC was administered as 1 capsule.

Interventions

OPC

The drug substance of 100 mg OPC was administered as 1 capsule.

Intervention Type: DRUG

Other Intervention Names

BIA 9-1067

Eligibility Criteria

Inclusion Criteria

1. Gender: male

2. Age: 18 - 55 years, inclusive

3. Body Mass Index (BMI): 18.0 - 30.0 kg/m2, inclusive Body weight (kg)and height2 (m2)

4. Ability and willingness to abstain from alcohol, methylxanthine-containing beverages or food (coffee, tea, cola, chocolate, "powerdrinks") and grapefruit (juice) from 48 hours prior to entry in the clinical research centre until discharge

5. Medical history without major pathology

6. Resting supine blood pressure and a resting pulse rate showing no clinically relevant deviations as judged by the MI

7. Computerised (12-lead) electrocardiogram (ECG) recording without signs of clinically relevant pathology or showing no clinically relevant deviations as judged by the MI

8. Willingness to use adequate contraception from the time of dosing until 3 months after the follow-up visit

9. All values for haematology and for clinical chemistry tests of blood and urine within the normal range or showing no clinically relevant deviations as judged by the MI

10. Willingness to sign the written ICF

Exclusion Criteria

1. Evidence of clinically relevant pathology

2. Mental handicap

3. History of relevant drug and/or food allergies

4. Regular/routine treatment with non-topical medications within 30 days prior to entrance into the clinical research centre

5. Smoking (less than 60 days prior to drug administration)

6. History of alcohol abuse or drug addiction (including soft drugs like cannabis products)

7. Use of concomitant medication, except for acetaminophen (paracetamol), which was allowed up to 3 days before entrance into the clinical research centre. Multivitamins and vitamin C were allowed up to 7 days before entrance into the clinical research centre. All other medication (including over the counter medication, health supplements, and herbal remedies such as St. John's wort extract) was to be stopped at least 14 days prior to entrance into the clinical research centre

8. Participation in a drug study within 60 days prior to drug administration. Participation in more than 3 other drug studies in the 10 months preceding administration of study drug

9. Donation of more than 50 mL of blood within 60 days prior to drug administration. Donation of more than 1.5 litres of blood in the 10 months preceding administration of study drug

10. Participation in another ADME study with a radiation burden -0.1 mSv in the period of 1 year before the start of the study

11. Exposure to radiation for diagnostic reasons (except dental X-rays and plain X rays of thorax and bony skeleton - excluding spinal column), during work or during participation in a medical study in the previous year

12. Irregular defecation pattern (less than once per 2 days)

13. Positive screen on drugs of abuse (opiates, methadone, cocaine, amphetamines, cannabinoids, barbiturates, benzodiazepines, tricyclic antidepressants and alcohol)

14. Intake of more than 24 units of alcohol per week (1 unit of alcohol equals approximately 250 mL of beer, 100 mL of wine or 35 mL of spirits)

15. Positive screen on hepatitis B surface antigen (HBsAg)

16. Positive screen on anti-hepatitis C virus (HCV)

17. Positive screen on anti- human immunodeficiency virus (HIV) 1/2

18. Illness within 5 days prior to drug administration

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Bial - Portela C S.A.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

PRA

Zuidlaren, , Netherlands

Countries

Netherlands

Other Identifiers

BIA-91067-122

Identifier Type: -

Identifier Source: org_study_id