Have a BMI of 19-42 kg/m2 (Click here to calculate)
Be diagnosed with Type 1 or Type 2 Diabetes
Be on stable dose of insulin or antidiabetic medication for at least 3 months
Have a history of Diabetic Peripheral Neuropathy
Be willing to be an inpatient (overnight stays) for the required time during study period
Not have a history of asthma as an adult
Not have uncontrolled or unstable High Blood Pressure
Not have a history of clinically significant drug, food allergy, skin allergy
Not have a history of moderate to severe depression, neurological or mental disorder not related to neuropathic pain
Not have a history of drug or alcohol abuse within the 6 months
Not consume more than 5 cigarettes per day within 30 days before study drug dosing or who cannot stop using any tobacco- or nicotine-containing product during the duration of the trial
Not have a documented history of HIV or positive test for HIV-1, HIV-2, active HBV, active HCV
Not have donated over 500mL of blood in the last 2 months
Not have participated in an investigational study within the last 30 days
If you are a woman of childbearing potential or a man whose partner is of childbearing potential, you must agree to use effective birth control
Males must not donate sperm until 90 days after the last dose of the study drug and must be willing to use a condom during heterosexual activity for up to 90 days after the application of the study drug
Not have participated in another investigational drug or device study within the past 30 day
Additional criteria will apply
PLEASE NOTE: Please confirm your eligibility before your appointment by calling +1 210-949-0122
If you do not see an available appointment, please call +1 210-949-0122 for availability.
Transportation may be available. Call +1 210-949-0122 . Compensation up to $5,825 is available for time and travel.
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