Daclizumab Japanese PK Study
Phase 1
Completed
- Conditions
- Healthy
- Interventions
- Biological: BIIB019 subcutaneous injection
- Registration Number
- NCT01929746
- Lead Sponsor
- Biogen
- Brief Summary
The primary objective of the study is to evaluate the pharmacokinetic (PK) profile of BIIB019 (Daclizumab High Yield Process; DAC HYP) administered as a single subcutaneous (SC) dose (75 mg or 150 mg) Japanese and Caucasian adult healthy volunteers. The secondary objective of this study in this study population is to assess the safety and tolerability of BIIB019 administered as a single SC dose (75 mg or 150 mg).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 56
Inclusion Criteria
- Japanese subjects must have been born in Japan, have both parents and grandparents of Japanese origin, and not have lived outside of Japan for more than 5 years or significantly modified their diets since leaving Japan.
- Subjects of childbearing potential must practice effective contraception during the study and be willing and able to continue contraception for at least 4 months after their last dose of study treatment.
- Body mass index (BMI) within 18 to 30 kg/m2, inclusive.
- Nonsmoker or be willing to abstain from using tobacco and tobacco-containing products for 24 hours prior to clinic admission and during the In-Clinic Period and to smoke no more than 10 cigarettes per day throughout the remainder of the study.
- Must be willing to refrain from all alcohol consumption for 48 hours prior to Day 1 and during the In-Clinic Period and to limit the intake of alcohol to no more than 2 units per day throughout the remainder of the study.
Key
Exclusion Criteria
- History of a positive test result for human immunodeficiency virus (HIV) antibody.
- History of hepatitis or a positive test result for hepatitis C virus antibody (HCVAb) or hepatitis B virus antibody (test for hepatitis B surface antigen [HBsAg] and/or hepatitis B core antibody [HBcAb]).
- History of tuberculosis (TB) or a positive QuantiFERON®-TB Gold test. There must be no other clinical evidence of TB on physical examination of the subject. Note: Subjects who have had prior adequate prophylaxis treatment for latent TB with an appropriate course of isoniazid or equivalent, per country standards, are not excluded from study participation.
- Subjects with a history of carcinoma in situ and malignant disease, with the exception of basal cell carcinoma that has been completely excised prior to study, are not eligible.
- Treatment with any prescription medication within 2 weeks before Day -1 with the exception of oral contraceptives for women of childbearing potential.
- Treatment with any nonprescription medicinal products (including vitamin/mineral/herbal-containing preparations but excluding acetaminophen) within the 7 days prior to study treatment.
NOTE: Other protocol-defined inclusion/exclusion criteria may apply.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description BIIB019, 75 mg BIIB019 subcutaneous injection BIIB019 delivered via Subcutaneous Injection BIIB019, 150 mg BIIB019 subcutaneous injection BIIB019 delivered via Subcutaneous Injection
- Primary Outcome Measures
Name Time Method Terminal elimination half-life (t1/2) Up to Day 105 Apparent volume of distribution (Vd/F) Up to Day 105 Area under the concentration-time curve from time 0 to infinity (AUCinf) Up to Day 105 Maximum observed concentration (Cmax) Up to Day 105 Time to reach maximum observed concentration (Tmax) Up to Day 105 Apparent clearance (CL/F) Up to Day 105
- Secondary Outcome Measures
Name Time Method The number of participants that experience Adverse Events (AEs) and Serious Adverse Events (SAEs) Up to Day 105
Trial Locations
- Locations (1)
Research Site
🇬🇧Leeds, United Kingdom