Pharmacokinetic and Safety Study with Adalimumab in Chinese Subjects with Mild Rheumatoid Arthritis
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
40 mg single sc dose
80 mg single sc dose
Site Reference ID/Investigator# 7181
Shanghai, China
pharmacokinetic profile of a single subcutaneous dose of 40 and 80 mg adalimumab
Time frame: Days 1, 2, 4, 6, 8, 11, 15, 22, & 29
Adverse event profile
Time frame: follow up to day 70 after dose
VAS assessments
Time frame: Days 1, 15 and 29
Swollen and Tender Joint counts
Time frame: Days 1, 15 and 29
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