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Tolerability, Pharmacokinetics and Pharmacodynamics of BIA 9-1067

Primary Purpose

Parkinson's Disease (PD)

Status
Completed
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
BIA 9-1067
Placebo
Sponsored by
Bial - Portela C S.A.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson's Disease (PD) focused on measuring Parkinson's disease (PD), Opicapone, Bial, BIA 9-1067

Eligibility Criteria

18 Years - 45 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. A signed and dated informed consent form before any study-specific screening procedure is performed.
  2. Aged between 18 and 45 years, inclusive.
  3. Healthy as determined by the investigator on the basis of medical history, physical examination, clinical laboratory test results, vital signs and digital 12-lead electrocardiogram (ECG).
  4. Nonsmoker or smoker of fewer than 10 cigarettes per day as determined by history. Must be able to abstain from smoking during the inpatient stay.

Exclusion Criteria:

  1. Any significant cardiovascular (e.g. hypertension), hepatic, renal, respiratory (e.g. childhood asthma), gastrointestinal, endocrine (e.g. diabetes, dyslipidemia), immunologic, dermatological, haematological, neurologic, or psychiatric disease.
  2. Acute disease state (e.g., nausea, vomiting, fever, diarrhoea) within 7 days before study day 1.
  3. History of drug abuse within 1 year before study day 1.
  4. History of alcoholism within 1 year before day 1. Consumption of more than 50 g of ethanol per day (12.5 cL glass of 10° [10%] wine = 12 g; 4 cL of aperitif, 42° [42%] whiskey = 17 g; 25 cL glass of 3° [3%] beer = 7.5 g; 25 cL glass of 6° [6%] beer = 15 g
  5. Have previously received BIA 9-1067.
  6. Positive serologic findings for human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg), and/or hepatitis C virus (HCV) antibodies.
  7. Positive findings of urine drug screen (eg, amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine, methadone, opiates, MDMA [3,4-methylenedioxy-methamphetamine; ecstasy]).
  8. History of any clinically important drug allergy.
  9. Prohibited Treatments: use of any investigational drug within 90 days or prescription drug within 30 days before investigational medical product (IMP) administration.
  10. Consumption of any caffeine-containing products (e.g., coffee, tea, chocolate, or soda) in excess of 6 cups per day (or equivalent), of grapefruit, grapefruit-containing products, or alcoholic beverages within 24 before study day 1.
  11. Use of any over-the-counter drugs including herbal supplements (except for the occasional use of acetaminophen [paracetamol], aspirin and vitamins ≤100% recommended daily allowance) within 7 days before IMP administration.
  12. Donation of blood (ie 450 ml) within 90 days before study day 1.

Sites / Locations

  • BIOTRIAL

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

BIA 9-1067 5 mg

BIA 9-1067 10 mg

BIA 9-1067 20 mg

BIA 9-1067 30 mg

Placebo

Arm Description

BIA 9-1067 (OPC, Opicapone) 5 mg

BIA 9-1067 (OPC, Opicapone) 10 mg

BIA 9-1067 (OPC, Opicapone) 20 mg

BIA 9-1067 (OPC, Opicapone) 30 mg

Placebo, PLC

Outcomes

Primary Outcome Measures

Number of Patients With at Least One Adverse Event

Secondary Outcome Measures

Full Information

First Posted
January 19, 2012
Last Updated
November 23, 2015
Sponsor
Bial - Portela C S.A.
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1. Study Identification

Unique Protocol Identification Number
NCT02071810
Brief Title
Tolerability, Pharmacokinetics and Pharmacodynamics of BIA 9-1067
Official Title
A Double-blind, Randomised, Placebo-controlled Study to Evaluate the Tolerability, Pharmacokinetics and Pharmacodynamics of Four Multiple Rising Dose Regimens of BIA 9-1067 in Healthy Male Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bial - Portela C S.A.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to assess the tolerability of BIA 9-1067 after multiple rising dose regimens of BIA 9-1067.
Detailed Description
Single centre, double-blind, randomised, placebo-controlled study of four dosage regimens of BIA 9-1067 in four groups of healthy male volunteers. In each group, the study will consist of an once-daily (o.d.) 8-day multiple-dose period. Progression to the next dose level will only occur if the previous dose level was considered to be safe and well tolerated. An appropriate interval (will separate the investigation of doses to permit a timely review and evaluation of safety data prior to proceeding to a higher dose level.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease (PD)
Keywords
Parkinson's disease (PD), Opicapone, Bial, BIA 9-1067

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BIA 9-1067 5 mg
Arm Type
Experimental
Arm Description
BIA 9-1067 (OPC, Opicapone) 5 mg
Arm Title
BIA 9-1067 10 mg
Arm Type
Experimental
Arm Description
BIA 9-1067 (OPC, Opicapone) 10 mg
Arm Title
BIA 9-1067 20 mg
Arm Type
Experimental
Arm Description
BIA 9-1067 (OPC, Opicapone) 20 mg
Arm Title
BIA 9-1067 30 mg
Arm Type
Experimental
Arm Description
BIA 9-1067 (OPC, Opicapone) 30 mg
Arm Title
Placebo
Arm Type
Experimental
Arm Description
Placebo, PLC
Intervention Type
Drug
Intervention Name(s)
BIA 9-1067
Other Intervention Name(s)
OPC, Opicapone
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
PLC, Placebo
Primary Outcome Measure Information:
Title
Number of Patients With at Least One Adverse Event
Time Frame
participants will be followed for the duration of hospital stay, an expected average of 6 weeks

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A signed and dated informed consent form before any study-specific screening procedure is performed. Aged between 18 and 45 years, inclusive. Healthy as determined by the investigator on the basis of medical history, physical examination, clinical laboratory test results, vital signs and digital 12-lead electrocardiogram (ECG). Nonsmoker or smoker of fewer than 10 cigarettes per day as determined by history. Must be able to abstain from smoking during the inpatient stay. Exclusion Criteria: Any significant cardiovascular (e.g. hypertension), hepatic, renal, respiratory (e.g. childhood asthma), gastrointestinal, endocrine (e.g. diabetes, dyslipidemia), immunologic, dermatological, haematological, neurologic, or psychiatric disease. Acute disease state (e.g., nausea, vomiting, fever, diarrhoea) within 7 days before study day 1. History of drug abuse within 1 year before study day 1. History of alcoholism within 1 year before day 1. Consumption of more than 50 g of ethanol per day (12.5 cL glass of 10° [10%] wine = 12 g; 4 cL of aperitif, 42° [42%] whiskey = 17 g; 25 cL glass of 3° [3%] beer = 7.5 g; 25 cL glass of 6° [6%] beer = 15 g Have previously received BIA 9-1067. Positive serologic findings for human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg), and/or hepatitis C virus (HCV) antibodies. Positive findings of urine drug screen (eg, amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine, methadone, opiates, MDMA [3,4-methylenedioxy-methamphetamine; ecstasy]). History of any clinically important drug allergy. Prohibited Treatments: use of any investigational drug within 90 days or prescription drug within 30 days before investigational medical product (IMP) administration. Consumption of any caffeine-containing products (e.g., coffee, tea, chocolate, or soda) in excess of 6 cups per day (or equivalent), of grapefruit, grapefruit-containing products, or alcoholic beverages within 24 before study day 1. Use of any over-the-counter drugs including herbal supplements (except for the occasional use of acetaminophen [paracetamol], aspirin and vitamins ≤100% recommended daily allowance) within 7 days before IMP administration. Donation of blood (ie 450 ml) within 90 days before study day 1.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dikran Mouradian, MD
Organizational Affiliation
Biotrial
Official's Role
Principal Investigator
Facility Information:
Facility Name
BIOTRIAL
City
Rueil
State/Province
Malmaison
ZIP/Postal Code
F-92501
Country
France

12. IPD Sharing Statement

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Tolerability, Pharmacokinetics and Pharmacodynamics of BIA 9-1067

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