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. 2024 Apr 24;230(3):624–634. doi: 10.1093/infdis/jiae198

Table 1.

Demographic and Clinical Characteristics of the Study Population at Baseline

Placebo Remdesivir
Included (n = 319) Total (n = 516) Included (n = 323) Total (n = 532)
Age, y, median (IQR) 59 (47-68) 60 (49-70) 59 (48-69) 59 (49-69)
Male sex 205 (64.26) 328 (63.57) 210 (65.02) 347 (65.23)
Race and ethnicity
Asian 30 (9.40) 56 (10.85) 42 (13.00) 79 (14.85)
Black or African American 84 (26.33) 114 (22.09) 73 (22.60) 105 (19.74)
White 167 (52.35) 286 (55.43) 168 (52.01) 273 (51.32)
Ethnicity: Hispanic or Latino 69 (21.63) 114 (22.09) 89 (27.55) 132 (24.81)
Clinical characteristics
Any comorbidities 255 (79.94) 417 (80.81) 271 (83.90) 435 (81.77)
Days of symptoms, median (IQR) 9 (7-13) 9 (7-13) 9 (6-12) 9 (6-12)
Baseline ordinal scale a
4 38 (11.91) 63 (12.21) 39 (12.07) 75 (14.10)
5 114 (35.74) 202 (39.15) 148 (45.82) 231 (43.42)
6 56 (17.55) 98 (18.99) 42 (13.00) 94 (17.67)
7 111 (34.80) 153 (29.65) 94 (29.10) 132 (24.81)
Disease severity subgroups b
Moderate/severe 152 (47.65) 265 (51.36) 187 (57.89) 306 (57.52)
Critical 167 (52.35) 251 (48.64) 136 (42.11) 226 (42.48)

Patients in our primary biomarker analysis cohort (Included) vs all patients from the original Adaptive COVID-19 Treatment Trial 1 (Total). Data are presented as No. (%) unless noted otherwise.

aNational Institute of Allergy and Infectious Diseases categorization of COVID-19 disease severity.

bModerate/severe disease is a combined subgroup of ordinal scales 4 and 5. Critical disease is a combined subgroup of ordinal scales 6 and 7.