Table 1 Demographics for the included participants

From: Randomized controlled trial of molnupiravir SARS-CoV-2 viral and antibody response in at-risk adult outpatients

Variable

Molnupiravir (n = 253)

Usual Care (n = 324)

P-value

Intensive sampling (%)

38 (15%)

42 (13%)

0.557

Median number of viral load measurements per participant intensive group (range)

8 (4,8)

8 (4,8)

–

Median number of viral load measurements per participant less-intensive group (range)

3 (1,3)

3 (1,3)

–

Median number of spike antibody measurements per participant (range)

3 (0,3)

3 (0,3)

–

Age years (sd)

58 (10.1)

58 (10.9)

0.844

Female (%)

139 (55%)

212 (65%)

0.0133

Ethnicity non-white (%)

7 (3%)

9 (3%)

>0.999

Fully vaccinated (≥3 doses) (%)

240 (95%)

314 (97%)

0.3

Inhaled corticosteroids (%)

56 (22%)

70 (22%)

0.959

Immune disease (%)

23 (9%)

21 (6%)

0.311

Obesity (%)

43 (17%)

46 (14%)

0.419

Any comorbidity (%)

167 (66%)

199 (61%)

0.294

PANORAMIC primary outcome: Hospitalised or died (%)

2 (0.79%)

3 (0.93%)

>0.999

Mean days since symptom onset at baseline (sd)

2.4 (0.78)

2.5 (1.12)

0.621

Mean viral load (log10(cp/mL)) at baseline (sd)

7.4 (1.14)

7.3 (1.04)

0.334

Mean spike antibody (log10(U/mL)) at baseline (sd)

3.3 (0.45)

3.3 (0.44)

0.91

Mean capillary CRP (mg/L) at baseline (sd)

0.68 (0.65)

0.65 (0.64)

0.544

  1. Continuous variables are reported as mean and standard deviation apart from the number of measurements which are reported as mean (range). Categorical variables reported as number in each category and percentage. Comparisons between molnupiravir and usual care arm variables was made using a t test for continuous variables and a Chi square test for categorical variables