The purpose of this study is to evaluate long-term safety and tolerability of dapirolizumab pegol treatment.
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Incidence of treatment-emergent adverse events (TEAEs) during the study
Timeframe: From Baseline (Day 1) until Safety Follow-Up (up to Week 110)
Incidence of serious treatment-emergent adverse events during the study
Timeframe: From Baseline (Day 1) until Safety Follow-Up (up to Week 110)
Incidence of treatment-emergent adverse events (TEAEs) leading to permanent dapirolizumab pegol discontinuation
Timeframe: From Baseline (Day 1) until Safety Follow-Up (up to Week 110)