{"description":"Safety evaluable population=all participants who received any part of blinded infusion of Obinutuzumab/placebo \\& are grouped according to treatment they received. 3 participants from placebo arm did not receive treatment \\& were excluded from the safety analysis. 1 participant randomized to placebo arm received obinutuzumab \\& was included in obinutuzumab arm for safety analysis. Includes AEs until point of rescue for participants who received rescue therapy (except corticosteroid-only rescue).","eventGroups":[{"deathsNumAffected":5,"deathsNumAtRisk":136,"description":"Participants received obinutuzumab, 1000 mg as an IV infusion on Day 1 and Weeks 2, 24, 26, and either Weeks 50 and 52 or Week 52 only, along with MMF and SOC therapy. Placebo was administered at Week 50 for participants not treated with obinutuzumab. Participants with adequate response at Week 76 continued to receive obinutuzumab at Week 80 and Q6M thereafter. The dose of MMF can be adjusted at the investigator's discretion beginning at Week 80.","id":"EG000","otherNumAffected":107,"otherNumAtRisk":136,"seriousNumAffected":44,"seriousNumAtRisk":136,"title":"Obinutuzumab"},{"deathsNumAffected":4,"deathsNumAtRisk":132,"description":"Participants received Obinutuzumab matching placebo as an IV infusion on Day 1 and Weeks 2, 24, 26, 50, and 52. Participants also received SOC therapy and MMF. Participants with adequate response at Week 76 continued to receive placebo at Week 80 and Q6M thereafter.","id":"EG001","otherNumAffected":94,"otherNumAtRisk":132,"seriousNumAffected":24,"seriousNumAtRisk":132,"title":"Placebo"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 27.0","stats":[{"groupId":"EG000","numAffected":7,"numAtRisk":136,"numEvents":7},{"groupId":"EG001","numAffected":9,"numAtRisk":132,"numEvents":10}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 27.0","stats":[{"groupId":"EG000","numAffected":7,"numAtRisk":136,"numEvents":10},{"groupId":"EG001","numAffected":6,"numAtRisk":132,"numEvents":8}],"term":"Leukopenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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Data collection post Week 76 is still ongoing. Final data will be reported 1 year after the study completion date. As pre-specified in the SAP, safety data were to be provided for obinutuzumab (combined treatment groups) and placebo groups. AE data were collected for all Obinutuzumab participants together, without regard to or information of the specific Obinutuzumab group participants they were part of."}