Patients were treated

with anidulafungin (±oral voriconaz

Patients were treated

with anidulafungin (±oral voriconazole) for 14–42 days. Patients not achieving negative blood/tissue cultures by day 7 were considered treatment failures and discontinued from the selleck products study. The primary endpoint was global response rate at the end of treatment (EOT) based on the modified intent-to-treat (MITT) population, which included patients who received any dose of study medication with confirmed candidaemia (positive blood culture) or invasive candidiasis (histopathological or cytopathological examination of a needle aspiration or biopsy specimen from a normally sterile site excluding mucous membranes showing yeast cells) within the 96 h before study entry. For the primary analysis, missing/indeterminate results were set to failure. Successful global response was defined as clinical success (cure/improvement – resolution/significant but incomplete resolution of signs and symptoms of candidaemia) and microbiological success (eradication – negative culture for Candida spp. present at baseline, or presumed eradication if follow-up cultures were not available, but clinical outcome was deemed a success). Key secondary endpoints included the following: global response rate at the end of IV therapy and at a week 2 follow-up assessment; all-cause mortality; incidence of adverse events

(AEs) and Opaganib in vitro discontinuations from the study; and change from baseline in clinical and laboratory parameters. The safety population included all patients who received any dose of medication. All serious adverse events (SAEs) and AEs were reported by the investigator in a case report form. The investigator was responsible for determining the causality of AEs. Laboratory evaluations

and clinical assessments including vital signs data, physical examination, bodyweight and height and APACHE II scores were also monitored. The sample size calculation was based on the desired precision (width of a two-sided 95% confidence interval [CI]) triclocarban for the estimate of a successful global response. The study required 147 patients if the expected global response rate was 70%, with the precision level of 7.3% (half width of a two-sided 95% CI for the incidence rate) using normal approximation. Assuming an evaluability rate of 70%, ~210 patients were targeted for enrolment in the study. The primary endpoint and key secondary endpoints of this study were summarised using descriptive statistics (number of patients, per cent, and 95% CI). In exploratory analyses of patient characteristics and response to treatment, the subgroups of patients who were or were not able to step-down to voriconazole were compared using Fisher’s Exact Test[16] to a significance level of P < 0.

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