A Study of M207 With Intranasal Zolmitriptan in Healthy Volunteers

Exclusion Criteria

• •1. Evidence of significant history of hepatic, reproductive, gastrointestinal, renal, bleeding, or hematological disorders including coagulation, pulmonary, neurological, respiratory, endocrine, or cardiovascular system abnormalities (especially hypertension, peripheral vascular disease, coronary artery disease, transient ischemic attacks, or cardiac rhythm abnormalities), psychiatric disorders, acute infection, or other conditions that would interfere with study participation or with the absorption, distribution, metabolism, or excretion of drugs.
• •2. Presence of two or more risk factors for cardiovascular disease (family history of premature heart disease, hyperlipidemia, or hypertension)
• •3. Any contraindication to zolmitriptan administration including:
• •* History of coronary artery disease or coronary vasospasm
• •* Symptomatic Wolf-Parkinson-White syndrome or other cardiac accessory conduction pathway disorders
• •* History of stroke, transient ischemic attack, or hemiplegic or basilar migraine
• •* Peripheral Vascular Disease
• •* Ischemic bowel disease
• •* Uncontrolled hypertension
• •* Any history of hepatic impairment
• •4. History of contact dermatitis or known dermatological disorders that would interfere with the study procedures or assessments
• •5. Planned participation in activities which cause inflammation, irritation, sunburn, lesions, or tattoos at the intended application sites from 2 weeks prior to screening through their last day of study participation
• •6. Use of warfarin within 1 month prior to the first dose or heparin within 1 week prior to study drug administration
• •7. Use of prescription and over the counter medications other than the following:
• •* Hormone Replacement Therapy (HRT)
• •* Birth control pills, patches, injections, or implants (all hormonal contraceptives) are allowed provided the dose has been stable for at least one month prior to screening and may be continued throughout the study
• •* Antihistamines
• •* Intermittently used NSAIDS
• •* Acetaminophen if medically necessary (not more than 2 g/day)
• •* Exceptions may be allowed on a case by case basis
• •8. Subjects who have a known allergy or sensitivity to zolmitriptan or its derivatives or formulations
• •9. Known allergy or sensitivity to tapes, adhesives, or zolmitriptan
• •10. Regular or recent intake of prescription drugs, particularly drugs with an influence on blood pressure.
• •11. Use of any other investigational compound within one month of planned study drug dosing
• •12. On-going drug or alcohol abuse, or history of either deemed to be clinically significant by the investigator
• •13. Systolic BP (measured after remaining sitting for 5 minutes) greater than 140 mmHg and diastolic BP greater than 90 mmHg at screening
• •14. History of nasal pathology (e.g., polyps) or abnormal nasal exam
• •15. Body Mass Index (BMI) greater than 35 kg/m2
• •16. If, in the opinion of the investigator, the subject is not suitable for the study
• •17. Any positive urine drug screen result or alcohol breath test