Pharmacokinetic Study in Healthy Males

Parkinson's Disease Clinical Trial

— NOCOF  

Official title:

Pharmacokinetics of Levodopa, Carbidopa, 3-OMD and ODM-104 After Repeated Doses of Different Formulations: an Open, Randomised, Multicentre Study With Crossover Design in Healthy Males

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02312232
• Other study ID #: 3112002
• Status: Completed
• Phase: Phase 1
• First received: December 2, 2014
• Last updated: February 17, 2015
• Start date: November 2014
• Est. completion date: February 2015

Study information

• Verified date: February 2015
• Source: Orion Corporation, Orion Pharma
• Contact: n/a
• Is FDA regulated: No
• Health authority: Finland: Finnish Medicines Agency
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to investigate the pharmacokinetics of levodopa, carbidopa, 3-OMD and ODM-104 after repeated doses of 3 levodopa formulations given in combination with carbidopa and ODM-104.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: February 2015
• Est. primary completion date: February 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Written informed consent (IC) obtained.

• Good general health ascertained by detailed medical history and physical examinations.

• Finnish speaking males 18-65 years of age (inclusive).

• Normal weight defined as a body mass index (BMI) > 19 and < 32 kg/m2 (BMI = weight/height2).

• Weight at least 60 kg.

• Regular intestinal transit (no recent history of recurrent constipation, diarrhoea, or other intestinal problems).

• Participants with female partners of child-bearing potential must adhere to a proper form of contraception (hormonal contraception or intrauterine device on female partner, and an additional barrier method used at least by one of the partners) from the first study treatment administration until 3 months after the end-of-study visit.

Exclusion Criteria:

• Evidence of clinically significant cardiovascular, renal, hepatic, haematological, gastrointestinal, pulmonary, metabolic-endocrine, malignancy, neurological or psychiatric disease within the previous 2 years.

• Inherited or family history (parents, siblings) of clinically significant cardiac conduction disease.

• Current/history of inflammatory bowel disease (IBDs): Colitis ulcerosa and Crohn's disease, celiac disease. Acute duodenal or gastric ulcer or gastritis, esophagitis, colon polyps or anal fissure.

• Any condition requiring regular concomitant treatment (including vitamins and herbal products) or likely to need any concomitant treatment during the study. As an exception, paracetamol for occasional pain is allowed.

• Intake of any medication that could affect the outcome of the study.

• Any clinically significant abnormal laboratory value or physical finding (including ECG and vital signs) that in the opinion of the investigator may interfere with the interpretation of study results or constitute a health risk for the subject if he takes part in the study.

• Known hypersensitivity to the active substances or the excipients of the drugs.

• History of vasovagal collapses or vagal reactions with unexplained reason within 2 years or a tendency for vasovagal reactions during blood sampling.

• History of sleep apnea.

• Heart rate (HR) < 40 bpm or > 90 bpm after 10 minutes in supine position at the screening visit and predose.

• At the screening visit:

systolic blood pressure (BP) < 90 mmHg or > 150 mmHg after 10 minutes in supine position diastolic BP < 50 mmHg or > 90 mmHg after 10 minutes in supine position

• Abnormal 24-hour Holter findings of clinical relevance according to cardiologist´s assessment at the screening visit.

• History of anaphylactic/anaphylactoid reactions.

• History of seizures excluding febrile seizures during the first 6 years of life.

• Strong tendency to motion sickness.

• Recent or current (suspected) drug abuse.

• Recent or current alcohol abuse; regular drinking of more than 21 units per week (1 unit = 4 cl spirits or equivalent).

• Current use of nicotine containing products more than 5 cigarettes (or equivalent)/day and/or inability to refrain from the use of nicotine containing products during the study (from the screening visit to the end-of-study visit).

• Use of caffeine containing beverages more than 600 mg of caffeine/day and/or inability to refrain from the use of caffeine containing beverages during the treatment periods until 24 hours after study treatment administration.

• Blood donation or loss of significant amount of blood within 90 days prior to the first study treatment administration.

• Administration of another investigational drug within 90 days prior to the first study treatment administration.

• Unsuitable veins for repeated venipuncture or for cannulation.

• Predictable poor compliance or inability to communicate well with the study centre personnel.

• Inability to participate in all treatment periods.

• Participation in a clinical drug study during or within 3 months prior to the first study treatment administration.

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Parkinson Disease
• Parkinson's Disease

Intervention

Drug:
• levodopa, carbidopa, ODM-104

Locations

Country	Name	City	State
Finland	CRST	Turku

Sponsors (1)

Lead Sponsor	Collaborator
Orion Corporation, Orion Pharma

Country where clinical trial is conducted

Finland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pharmacokinetics (Cmax) of levodopa	Peak Plasma Concentration (Cmax)	24 hours	No
Secondary	Pharmacokinetics (Cmax) of carbidopa, 3-OMD and ODM-104	Peak Plasma Concentration (Cmax)	24 hours	No