This study is being conducted to evaluate the pharmacokinetics, safety, and tolerability of INCA033989 following subcutaneous (SC) or intravenous administration (IV) n healthy adult participants.
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Pharmacokinetics Parameter: Cmax of INCA33989 following a single SC administration compared with a single IV infusion
Timeframe: Up to 12 weeks
Pharmacokinetics Parameter: AUClast of INCA33989 following a single SC administration compared with a single IV infusion
Timeframe: Up to 12 weeks
Pharmacokinetics Parameter: AUC0∞ of INCA33989 following a single SC administration compared with a single IV infusion
Timeframe: Up to 12 weeks
Number of participants with Treatment-emergent Adverse Events (TEAEs)
Timeframe: Up to 12 weeks