Open, Single Center, Three Periods, Fixed Sequence Design Study on the Effects of Clopidogrel Co-administration on the Pharmacokinetics of Neramexane

This study has been completed.
Sponsor:
Information provided by:
Merz Pharmaceuticals GmbH
ClinicalTrials.gov Identifier:
NCT00936026
First received: July 8, 2009
Last updated: February 7, 2011
Last verified: July 2009
  Purpose

Primary:

To assess the effects of CYP2B6 inhibition by repeated dose Clopidogrel (75 mg/day) co-administration on the single-dose pharmacokinetics of Neramexane

Secondary:

To assess safety and tolerability of Neramexane single dose treatment alone and co-administration of a Neramexane single-dose with a Clopidogrel repeated dose treatment


Condition Intervention Phase
Healthy Subjects
Drug: Neramexane
Phase 1

Study Type: Interventional
Study Design: Masking: Open Label

Further study details as provided by Merz Pharmaceuticals GmbH:

Study Start Date: July 2009
Study Completion Date: December 2009
Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: Neramexane
    Drug-Drug Interaction Study
  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Healthy adult subject of white origin, who is able to read, to write and fully understand German language
  2. Aged 18 to 45 years
  3. BMI of 18-28 kg/m2 and a body weight of 50-90 kg
  4. Willing and able to provide written informed consent after having been informed of the requirements and the restrictions of the study. Female subjects of childbearing potential must agree to use a highly effective method of birth control defined as those which result in a low failure rate (i.e. less than 1 % per year) when used consistently and correctly such as sexual abstinence, vasectomised partner, non hormonal IUDs, double barrier methods, for instance, e.g. condom and spermicide cream.

Exclusion Criteria:

  1. History of clinically relevant allergy or known hypersensitivity to Neramexane/ Memantine/Amantadine and their derivatives
  2. History of clinically relevant allergy or known hypersensitivity to Clopidogrel
  3. Exposure to another investigational agent within the last two months before Day 1 of Period 1
  4. History of clinically relevant allergy or known hypersensitivity to any inactive ingredient in any of the used investigational products or the metabolic inhibitor
  5. Lactating or pregnant females or females planning to become pregnant during study conduct or within 2 months after end of study
  6. Any contraindications which are indicated in the topically valid SPC for Plavix®: severe hepatic impairment; active pathological bleeding such as peptic ulcer or intracranial hemorrhage

    Lack of suitability for the trial:

  7. Any evidence of a significant cardiovascular, pulmonary, renal, hepatic, gastrointestinal, endocrinological, metabolic or other disease at screening
  8. History of malignancy
  9. Any clinically relevant deviation in clinical or laboratory assessment
  10. ECG abnormalities of clinical relevance, in particular abnormal prolongations of QT/QTc-interval (i.e. QTc ≥ 450 ms, PQ ≥ 220 ms)
  11. Systolic blood pressure <95 mmHg or >150 mmHg or diastolic blood pressure < 50 mmHg or >90 mmHg in supine position
  12. Pulse rate <45 or >100 beats per minute
  13. Chronic or acute clinically relevant infections
  14. Acute or chronic disease, especially psychiatric or neurologic disorders
  15. History of alcohol or drug dependence
  16. Alcohol consumption averaging more than 40 g for male and more than 20 g for female subjects daily within the last year
  17. Regular caffeine consumption averaging more than 1 L of coffee and/or tea daily or more than 1 L of caffeine-containing lemonades per day within the last year
  18. Disorders or surgery of the gastrointestinal tract which may interfere with drug absorption or may otherwise influence the pharmacokinetics of the investigational medicinal products (e.g. cholecystectomy, ulcus, etc.)
  19. Anticipated donation of spermatocytes or oocytes for medically assisted reproduction techniques [ART] within two months after the last dose of the present study
  20. Use of any prescribed medication for four weeks prior to the first administration of IMP.

    • Regular use of over-the-counter drugs in the 4 weeks prior to the first administration of the IMP
    • Occasional use of OTC drugs (except paracetamol, maximum 1 g/day) within the 2 weeks prior to the first administration of the IMP.
    • Stable intake of thyroid hormone substitution will be allowed.
  21. Use of any food, food supplement or medication known to induce or inhibit CYP3A4 or other cytochrome P450 enzymes within two weeks preceding the start of the study (Day 1), e.g. grapefruit, St. John's wort
  22. Female subjects who employed any form of hormonal contraception within 2 months prior to study Day 1 (e.g. oral contraceptives, hormone releasing intrauterine contraceptive devices [IUDs], etc.)
  23. Consumption of xanthine derivates (including caffeine) within two days prior to Day 1
  24. Smoker and user of snuff, nicotine replacement and chewing tobacco
  25. Previous enrolment into the clinical phase of the current study
  26. Positive results in any of the serology tests
  27. Blood donation more than 450 mL within 60 days prior to Day 1
  28. Positive pregnancy test, if female
  29. Positive drug screen or alcohol test
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00936026

Locations
Germany
AAIPharma Deutschland gmbH & Co. KG
Neu Ulm, Bayern, Germany, 89231
Sponsors and Collaborators
Merz Pharmaceuticals GmbH
  More Information

No publications provided

Responsible Party: Dr. med. Margarete Müller, AAIPharma Deutschland gmbH & Co. KG
ClinicalTrials.gov Identifier: NCT00936026     History of Changes
Other Study ID Numbers: MRZ 92579/TI/1002
Study First Received: July 8, 2009
Last Updated: February 7, 2011
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

ClinicalTrials.gov processed this record on August 26, 2014