The purpose of this study is to establish the tolerability, preliminary efficacy, and pharmacokinetics of CC-97540 in participants with severe, refractory autoimmune diseases (Breakfree-1).
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Number of participants with treatment-emergent adverse events (AEs) in each indication.
Timeframe: Up to 2 years after CC-97540 infusion
Number of participants with serious AEs (SAEs) in each indication.
Timeframe: Up to 2 years after CC-97540 infusion
Number of participants with AEs of special interest (AESI) in each indication.
Timeframe: Up to 2 years after CC-97540 infusion
Number of participants with laboratory abnormalities in each indication.
Timeframe: Up to 2 years after CC-97540 infusion
Number of participants with Dose Limiting Toxicities (DLT) in each indication.
Timeframe: Up to 2 years after CC-97540 infusion
Recommended Phase 2 Dose (RP2D) of CC-97540 in each indication.
Timeframe: Up to 2 years after CC-97540 infusion
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