{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","spread":"61.686","value":"23.42"},{"comment":"Only 1 participant is included in the analysis, therefore Standard deviation cannot be calculated.","groupId":"OG001","spread":"NA","value":"12.97"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"2"},{"groupId":"OG001","value":"1"}],"units":"Participants"}],"dispersionType":"Standard Deviation","groups":[{"description":"Tisotumab vedotin 0.9 mg/kg was administered as an intravenous infusion, over a minimum of 30 minutes, 3 times every 4 weeks (3q4wk).","id":"OG000","title":"Part 1: Dose Escalation: Cohort 1 3q4wk 0.9 mg/kg"},{"description":"Tisotumab vedotin 1.2 mg/kg was administered as an intravenous infusion, over a minimum of 30 minutes, 3 times every 4 weeks (3q4wk).","id":"OG001","title":"Part 1: Dose Escalation: Cohort 2 3q4wk 1.2 mg/kg"}],"paramType":"MEAN","populationDescription":"PSA is only assessed for participants with prostate cancer. 2 participants in Part 1 Cohort 1 and 1 participant in Part 1 Cohort 2 had the indication of prostate cancer.","reportingStatus":"POSTED","timeFrame":"Baseline to end of follow-up; maximum follow-up was 24 weeks","title":"Part 1: Response Evaluation Based on PSA (Prostate Specific Antigen [Prostate Cancer]): Percentage Change From Baseline to End of Study","type":"SECONDARY","unitOfMeasure":"percentage of change"}