Randomized study in healthy men and women. Assess the similarity of RO7239361 when injected into the arm, thigh, or the stomach. Collect data on safety of RO7239361.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
99
Specified dose on specified days
WCCT Global, Inc.
Cypress, California, United States
Maximum observed serum concentration (Cmax)
Time frame: Up to 92 days
AUC from time zero to time of last quantifiable concentration [AUC(0-T)]
Time frame: Up to 92 days
AUC from time zero extrapolated to infinite time [AUC(INF)]
Time frame: Up to 92 days
Incidence of Adverse Events ( AEs)
Time frame: Up to 92 days
Incidence of Serious Adverse Events (SAEs)
Time frame: Up to 92 days
Change from baseline in electrocardiogram findings
Time frame: Up to 92 days
Change from baseline in physical examination findings
Time frame: Up to 92 days
Change from baseline in clinical laboratory test findings
Time frame: Up to 92 days
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