Safety, Tolerability, and Pharmacokinetics of Single Doses of BIIB059 in Healthy Japanese Subjects.
Status: | Completed |
---|---|
Conditions: | Healthy Studies |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 18 - 55 |
Updated: | 9/2/2018 |
Start Date: | October 4, 2017 |
End Date: | June 12, 2018 |
A Blinded, Safety, Tolerability, and Pharmacokinetic Study of Single Doses of BIIB059 in Healthy Japanese Subjects
To assess the safety and tolerability of single, subcutaneous (SC) doses of BIIB059 in
healthy Japanese subjects.
healthy Japanese subjects.
Inclusion Criteria:
- Ability to understand the purpose and risks of the study and provide signed and dated
informed consent and authorization to use confidential health information in
accordance with national and local subject privacy regulations
- Must have been born in Japan, and both their biological parents and grandparents must
have been of Japanese origin
- Aged 18 to 55 years old, inclusive, at the time of informed consent, and must have a
body mass index between 18 and 30 kilogram per square meter (kg/m2), and a body weight
>45 kg
- All women of childbearing potential and all men must practice highly effective
contraception during the study and for 16 weeks after their dose of study treatment
Exclusion Criteria:
- History of any clinically significant cardiac, endocrine, gastrointestinal,
hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic,
dermatologic, psychiatric, or renal disease, or other major disease, as determined by
the Investigator
- History or positive test result for human immunodeficiency virus. Current active
hepatitis C virus infection (defined as hepatitis C virus RNA above the limit of
detection). Positive test result for hepatitis B virus (defined as positive for
hepatitis B surface antigen or hepatitis B core antibody). Chronic, recurrent, or
serious infection (e.g., pneumonia, septicemia), as determined by the Investigator,
within 90 days prior to Screening or between Screening and Day -1
- Clinically significant abnormal laboratory test values, as determined by the
Investigator, at Screening or Day -1
- Current enrollment or a plan to enroll in any interventional clinical study in which
an investigational treatment or approved therapy for investigational use is
administered within 5 half-lives prior to Day -1
- History of alcohol or substance abuse (as determined by the Investigator), a positive
urine drug or alcohol test at Screening or Day -1, an unwillingness to refrain from
illicit or recreational drugs, or an unwillingness to abide by the alcohol
restrictions
NOTE: Other protocol defined Inclusion/Exclusion criteria may apply
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