This trial is conducted in North America. The aim of this clinical trial is to investigate the safety, tolerability, pharmacokinetic and signs of bioactivity of increasing single doses of AGS-009 in patients with systemic lupus erythematosus (SLE).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
13
Unnamed facility
Birmingham, Alabama, United States
Unnamed facility
Kansas City, Kansas, United States
Unnamed facility
Lake Success, New York, United States
Unnamed facility
Durham, North Carolina, United States
Frequency of adverse events
Time frame: From dosing at visit 2 until end of safety visits at visit 8.
Pharmacokinetic - AUC (area under the curve)
Time frame: From dosing at visit 2 until end of safety visits at visit 8.
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Unnamed facility
Duncansville, Pennsylvania, United States
Unnamed facility
Dallas, Texas, United States