Open-label Phase 1b/2 study with primary objective of this study is to evaluate the safety, tolerability and efficacy of AZD0120 in participants with light chain (AL) amyloidosis.
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Phase 1b: Number of Participants With incidence and severity of Treatment-emergent Adverse Events
Timeframe: Through study completion, a minimum of 6 months
Phase 2: Proportion of Participants Experiencing a Complete Response
Timeframe: Through study completion, a minimum of 6 months
Alexion Pharmaceuticals, Inc. (Sponsor)