Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Healthy male or female
Age 18 - 55
Body mass index (BMI) ranging between 18 and 30 kg/m2, inclusive
Negative urine drug screen/alcohol breathalyzer results at Screening and at Day -1
Has not used tobacco products during the 3 months prior to Screening and agrees to refrain from use throughout the study duration
Female subjects of child-bearing potential must agree to use one of the study-approved effective contraceptive methods for the duration of the study and through 1 month after completion of the final study visit
Male subjects must be either surgically sterilized or agree to use study-approved effective contraceptive methods for the duration of the study and through 1 month after completion of the final study visit
If female, a negative serum pregnancy test at Screening and urinary pregnancy test at Day -1 is required
Able to read, understand, and provide signed informed consent
Able to communicate adequately with the investigator and to comply with the requirements for the entire study.

Exclusion Criteria:

Blood pressure ≥ 140/90 mmHg or pulse > 100 beats/minute at Screening
QTc intervals corrected for heart rate via the Fridericia method (QTcF) > 450 msec (males) and > 480 msec (females) at Screening
Pregnant or a nursing female
Male with a pregnant partner
Currently enrolled in another clinical trial or has received treatment with an investigational drug during the 30 days (or 5 half-lives, whichever is longer) prior to dosing
History of substance or alcohol abuse or dependency within the past
Used any medications or over the-counter products within 14 days or 5 half lives (whichever is longer) prior to administration of study medication, including analgesics, hormonal contraceptives (oral contraceptive pills or implant), natural food supplements, or dietary or herbal supplements including vitamins)
Donated blood in excess of 500 mL within 56 days prior to the dosing or intention of donating during the study through the month after completing the study
Positive test results for hepatitis B virus (HBV) surface antigen, hepatitis C virus antibody (HCV), or human immunodeficiency virus (HIV)
History or presence of any condition that, in the opinion of the Investigator, could interfere with the study conduct or observation
A medical history of or any current clinically significant disorder, including but not limited to: asthma, angioedema, bronchospasm, ulcer disease, gastrointestinal bleeding, coagulation defects, hypertension, edema, heart failure, hypokalemia, cardiovascular disease, hypersensitivity reaction to any biologic drug, significant dermatologic diseases or condition that would significantly influence the immune response
A serious illness, medical surgical procedure, or trauma resulting in missed work or hospitalization within the 30 days preceding the beginning of study treatment
Received treatment for any type of cancer within the 5 years prior to enrollment
An employee, family member, or student of the Investigator or clinical site