Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Impel Pharmaceuticals
Age
18–55
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Adult male and females, 18 to 55 years of age (inclusive) at the time of screening.
Subjects must be in good general health, with no significant medical history (including migraine), have no clinically significant abnormalities on physical examination at screening, and/or before administration of the initial dose of investigational product.
Subjects must have a Body Mass Index (BMI) between 18 and 32 kg/m2, inclusive.
Subjects must have clinical laboratory values within normal range as specified by the testing laboratory, or assessed as not clinically significant by the Principal Investigator.
Negative urine drug screen/alcohol breath test at screening.
Subjects who are willing to refrain from smoking for the duration of the study.
You may not be if
Subjects with a recent history of migraine and its variants including hemiplegic migraine and basilar migraine. A recent history of migraine is defined as (a) current or past history of migraine with at least 1 attack in last 6 months or (b) those receiving antimigraine prophylaxis.
Positive testing for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C antibodies (HCV).
Subjects who have ingested caffeine within 48 hours before admission on Day -1. Subjects must also agree to refrain from consumption of caffeinated drinks for 48 hours before admission of Days 7 and 14 (i.e. prior to each subsequent dosing), and throughout confinement.
Subjects with ischemic heart disease or subjects who have clinical symptoms or findings consistent with coronary artery vasospasm including Prinzmetal's variant angina.
Subjects with hypertension, known peripheral arterial disease, Raynaud's phenomenon, sepsis, history of vascular surgery or severely impaired hepatic or renal function
Subjects who have previously shown hypersensitivity to ergot alkaloids or metoclopramide.
Use of any relevant prescription, over-the-counter medication (with the exception of oral contraceptives), foods (e.g. grapefruit juice) or supplements (including herbal) within 14 days of randomization \[especially those affecting the Cytochrome P450 3A4 (CYP3A4) metabolic pathway\].
History or presence of alcoholism or drug abuse within the 2 years prior to the first investigational product administration.
Surgery within the past three months prior to the first investigational product administration as determined by the PI to be clinically relevant.
Active infection and/or use of macrolide antibiotics within 14 days prior to enrollment.
History of recurrent infections.
Any nasal congestion or physical blockage in either nostril, or deviated nasal septum as determined by nasal examination.
