{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","spread":"0.25","value":"-0.7"},{"groupId":"OG001","spread":"0.25","value":"-1.4"},{"groupId":"OG002","spread":"0.26","value":"-1.0"}]}],"title":"Change from Baseline at Week 1 [N=63; 63; 57]"},{"categories":[{"measurements":[{"groupId":"OG000","spread":"0.31","value":"-1.7"},{"groupId":"OG001","spread":"0.31","value":"-2.6"},{"groupId":"OG002","spread":"0.33","value":"-2.3"}]}],"title":"Change from Baseline at Week 4 [N=63; 62; 58]"},{"categories":[{"measurements":[{"groupId":"OG000","spread":"0.33","value":"-2.1"},{"groupId":"OG001","spread":"0.32","value":"-3.2"},{"groupId":"OG002","spread":"0.35","value":"-2.6"}]}],"title":"Change from Baseline at Week 8 [N=62; 63; 57]"},{"categories":[{"measurements":[{"groupId":"OG000","spread":"0.36","value":"-2.2"},{"groupId":"OG001","spread":"0.35","value":"-3.4"},{"groupId":"OG002","spread":"0.39","value":"-2.5"}]}],"title":"Change from Baseline at Week 12 [N=59; 61; 52]"},{"categories":[{"measurements":[{"groupId":"OG000","spread":"0.34","value":"-2.2"},{"groupId":"OG001","spread":"0.34","value":"-3.3"},{"groupId":"OG002","spread":"0.36","value":"-2.5"}]}],"title":"Change from Baseline at EOT [N=63; 64; 58]"}],"denoms":[{"counts":[{"groupId":"OG000","value":"63"},{"groupId":"OG001","value":"64"},{"groupId":"OG002","value":"58"}],"units":"Participants"}],"description":"The IPSS is a validated global questionnaire used to assess the degree of \"bother\" from benign prostatic hyperplasia symptoms based on the answers to 7 questions concerning urinary symptoms. Each question is assigned points from 0 to 5 indicating increasing severity of the particular symptom. The storage symptom score is the sum of the responses to 3 questions relating to storage symptoms (frequency, urgency and nocturia) and ranges from 0 to 15 (asymptomatic to very symptomatic).\n\nLeast squares means were derived from an ANCOVA model with the pooled study center and treatment as factors and the baseline value as a covariate.","dispersionType":"Standard Error","groups":[{"description":"Participants received matching mirabegron placebo tablets orally once daily for 12 weeks.","id":"OG000","title":"Placebo"},{"description":"Participants received 50 mg mirabegron tablets orally once daily for 12 weeks.","id":"OG001","title":"Mirabegron 50 mg"},{"description":"Participants received 100 mg mirabegron tablets orally once daily for 12 weeks.","id":"OG002","title":"Mirabegron 100 mg"}],"paramType":"LEAST_SQUARES_MEAN","populationDescription":"The Full Analysis Set included all patients who received at least 1 dose of double-blind study drug \\& had both Qmax \\& PdetQmax measurements at baseline \\& 1 or both at any postbaseline on-treatment visit. End of treatment (EOT) includes the last on-treatment assessment for patients who didn't complete Week 12; N is the number of patients included.","reportingStatus":"POSTED","timeFrame":"Baseline and Weeks 1, 4, 8 and 12","title":"Change From Baseline to Weeks 1, 4, 8, 12 and End of Treatment in International Prostate Symptoms Score (IPSS) Storage Symptom Score","type":"SECONDARY","unitOfMeasure":"scores on a scale"}