{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"1.81","upperLimit":"8.31","value":"4.11"},{"groupId":"OG001","lowerLimit":"1.28","upperLimit":"13.67","value":"6.70"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"30"},{"groupId":"OG001","value":"16"}],"units":"Participants"}],"title":"Postive"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"1.41","upperLimit":"2.63","value":"1.84"},{"groupId":"OG001","lowerLimit":"1.41","upperLimit":"3.02","value":"1.94"}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"129"},{"groupId":"OG001","value":"66"}],"units":"Participants"}],"title":"Negative"}],"denoms":[{"counts":[{"groupId":"OG000","value":"159"},{"groupId":"OG001","value":"82"}],"units":"Participants"}],"description":"the time from randomization to the date of first documented disease progression, or death due to any cause, whichever occurs first.\n\nProgressive Disease (PD): At least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. (Note: the appearance of one or more new lesions is also considered progression).","dispersionType":"95% Confidence Interval","groups":[{"description":"Participants with histologically confirmed Squamous Cell Carcinoma of the Head and Neck (SCCHN) that has recurred during or less than 6 months after completion of previous platinum-based chemotherapy.\n\nTreated with Nivolumab 3 mg/kg Q2W + Ipilimumab 1 mg/kg Q6W","id":"OG000","title":"Treatment A - Platinum Refractory Subgroup"},{"description":"Participants with histologically confirmed Squamous Cell Carcinoma of the Head and Neck (SCCHN) that has recurred during or less than 6 months after completion of previous platinum-based chemotherapy.\n\nTreated with Nivolumab 3 mg/kg Q2W + Ipilimumab-Placebo Q6W","id":"OG001","title":"Treatment B - Platinum Refractory Subgroup"}],"paramType":"MEDIAN","populationDescription":"Platinum Refractory subgroup all randomized","reportingStatus":"POSTED","timeFrame":"From randomization to disease progression or death. Approximately 63 Months","title":"Progression Free Survival (PFS) - Platinum Refractory Subgroup Based on HPV p-16 Status","type":"SECONDARY","unitOfMeasure":"Months"}