Table 4.
Treatment and Authors | Primary Endpoints | Efficacy (All Values in %) |
Dosing and Route of Administration |
---|---|---|---|
Paxlovid-Hammond et al. [131] | 28-day incidence all-cause hospitalization or mortality. | 0.7 Tx vs. 6.5 placebo; rRR, 88 (p < 0.0001). |
300 mg nirmatrelvir and 100 mg ritonavir oral BID × 5 days. |
Molnupiravir-Jayk Bernal et al. [132] | 29-day incidence all-cause hospitalization or mortality. | 6.8 Tx vs. 9.7 placebo; rRR, 30 (p = 0.022). |
800 mg at four 200 mg capsules oral BID × 5 days. |
Remdesivir-Gottlieb et al. [133] | 28-day incidence of all-cause hospitalization or mortality. | 0.7 Tx vs. 5.3 placebo; hazard ratio, 0.13 (p = 0.008). | 200 mg IV for 1 day, 100 mg IV, for next 2 days. |
Fluvoxamine-Reis et al. [134] | 28-day incidence of all-cause hospitalization, defined as retention in ER setting for >6 h or transfer to a tertiary hospital due to COVID-19. | 11.0 Tx vs. 16 placebo; rRR, 68.0 (p = 0.002). | 100 mg oral BID × 10 days. |
Convalescent Plasma–Sullivan et al. [135] | 28-day incidence of all-cause hospitalization | 2.9 Tx vs. 6.3 placebo; absolute risk reduction, 3.4; 95% CI, 1.0–5.8; p = 0.005 | 250 mL transfusion over 1 h, followed by 30 min of observation |
REGEN-COV- Weinreich et al. [136] |
29-day incidence of all-cause hospitalization or mortality. | 4.0 Tx vs. 3.2 placebo; rRR, 70.4 (p = 0.002). | 1200 mg single dose, IV (600 mg casirivimab, 600 mg imdevimab). |
Bamlanivimab/Etesevimab- Dougan et al. [137] |
29-day incidence of all-cause hospitalization or mortality. | 2.1 Tx vs. 7.0 placebo; rRR, 70.0 (p < 0.001). | 5600 mg single dose, IV (2800 mg bamlanivimab/2800 mg etesivimab). |
Sotrovimab Gupta et al. [138] |
29-day incidence of all-cause hospitalization or mortality. | 1.0 Tx vs. 7.0 placebo; rRR, 85.0 (p = 0.002). | 500 mg single dose, IV |
IV: intravenous, rRR: relative risk reduction, Tx: treatment.