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Fig. 2 | BMC Medicine

Fig. 2

From: A multicenter, double-blind, randomized, parallel-group, placebo-controlled study to evaluate the efficacy and safety of camostat mesilate in patients with COVID-19 (CANDLE study)

Fig. 2

Time to SARS-CoV-2 negative conversion (local laboratory tests). a The median time to negative conversion was estimated using the Kaplan–Meier method, and the confidence intervals were calculated using the Brookmeyer–Crowley method with double log transformation. b A Cox proportional hazards model stratified by the randomization factors (age group and underlying diseases) was used to determine the posterior mean hazard ratio with two-sided 95% credible intervals for the camostat mesilate group relative to the placebo group. c Stratified log-rank test with randomization factors (age group and underlying diseases) as stratification factors. d Cox proportional hazards model with randomization factors (age group and underlying diseases) as stratification factors and treatment group as the covariate. Age groups: ≥ 65 years vs < 65 years. Underlying diseases: chronic respiratory disease, chronic kidney disease, diabetes mellitus, hypertension, cardiovascular disease, and obesity (body mass index ≥ 30 kg/m2). n/c not calculable

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