Features and properties of regdanvimab
| Alternative names | CT-P59; Regkirona |
| Class | Antivirals; Monoclonal antibodies |
| Mechanism of action | Virus internalisation inhibitors |
| Route of administration | Intravenous infusion |
| Pharmacodynamics | Neutralizes severe acute respiratory syndrome coronavirus 2 by binding to the receptor binding domain of the virus’ spike protein; decreases viral load in upper and lower respiratory tracts in animal models |
| Pharmacokinetics | Dose-proportional pharmacokinetics over a dose range of 20–80 mg/kg; median time to maximum plasma concentration 2.5 h; low clearance (0.227 mL/kg for 40 mg/kg); small volume of distribution (87.2 mL/kg for 40 mg/kg); terminal half-life 12 days; eliminated through normal immunoglobulin degradation pathways |
| Most frequent adverse events | Hypertriglyceridemia |
| ATC codes | |
| WHO ATC code | J05A-X (Other antivirals) |
| EphMRA ATC code | J5B (Antivirals, excluding anti-HIV products) |
| CAS Registry Number | 2444308-95-4 |