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The Safety Set includes all participants who received any amount of 18F-DCFPyL. Data are presented for participants in Cohort A and Cohort B.","groups":[{"description":"Cohort A participants who had a follow-up laboratory value that was below the lower limit of normal. Cohort A were high risk cancer participants planned for radical prostatectomy with pelvic lymph node dissection.","id":"OG000","title":"Cohort A - Follow-up Value: Low"},{"description":"Cohort B participants who had a follow-up laboratory value that was below the lower limit of normal. Cohort B were participants with presumptive radiologic evidence of prostate cancer recurrence or metastasis on conventional imaging and planned conventional image-guided biopsy.","id":"OG001","title":"Cohort B - Follow-up Value: Low"},{"description":"Cohort A participants who had a follow-up laboratory value that was within normal limit. Cohort A were high risk cancer participants planned for radical prostatectomy with pelvic lymph node dissection.","id":"OG002","title":"Cohort A - Follow-up Value: Normal"},{"description":"Cohort B participants who had a follow-up laboratory value that was within normal limits. Cohort B were participants with presumptive radiologic evidence of prostate cancer recurrence or metastasis on conventional imaging and planned conventional image-guided biopsy.","id":"OG003","title":"Cohort B - Follow-up Value: Normal"},{"description":"Cohort A participants who had a follow-up laboratory value that was above the upper limit of normal. Cohort A were high risk cancer participants planned for radical prostatectomy with pelvic lymph node dissection.","id":"OG004","title":"Cohort A - Follow-up Value: High"},{"description":"Cohort B participants who had a follow-up laboratory value that was above the upper limit of normal. Cohort B were participants with presumptive radiologic evidence of prostate cancer recurrence or metastasis on conventional imaging and planned conventional image-guided biopsy.","id":"OG005","title":"Cohort B - Follow-up Value: High"},{"description":"Cohort A participants who did not have a follow-up laboratory value. Cohort A were high risk cancer participants planned for radical prostatectomy with pelvic lymph node dissection.","id":"OG006","title":"Cohort A - Follow-up Value: Missing"},{"description":"Cohort B participants who did not have a follow-up laboratory value. Cohort B were participants with presumptive radiologic evidence of prostate cancer recurrence or metastasis on conventional imaging and planned conventional image-guided biopsy.","id":"OG007","title":"Cohort B - Follow-up Value: Missing"}],"paramType":"COUNT_OF_PARTICIPANTS","populationDescription":"The Safety Set includes all participants who received any amount of 18F-DCFPyL.","reportingStatus":"POSTED","timeFrame":"From time of screening (baseline) until pre-surgery/biopsy (within 28 days post-study drug dosing).","title":"Shift From Baseline in Selected Clinical Chemistry Laboratory Values at Follow-up (Safety Outcome Measure)","type":"SECONDARY","unitOfMeasure":"Participants"}