The objective of this study is to evaluate the safety, tolerability, immunogenicity and pharmacokinetics (PK ) properties following a single dose of ABBV-277 in healthy adult participants.
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Maximum Plasma Concentration (Cmax) of ABBV-277
Timeframe: Up to approximately 9 days
Time to Cmax (Tmax) of ABBV-277
Timeframe: Up to approximately 9 days
Terminal Phase Elimination Rate Constant (Beta) of ABBV-277
Timeframe: Up to approximately 9 days
Terminal Phase Elimination Half-Life (t1/2) of ABBV-277
Timeframe: Up to approximately 9 days
Area Under the Concentration-Time Curve From Time 0 to Time t (AUCt) of ABBV-277
Timeframe: Up to approximately 9 days
Area Under the Concentration-Time Curve From Time 0 to Infinity (AUCinf) of ABBV-277
Timeframe: Up to approximately 9 days
Number of Participants With Adverse Events (AEs)
Timeframe: Up to Day 196