This is a phase 2, randomized, multiple-dose, placebo-controlled study designed to evaluate the safety, efficacy, and pharmacokinetics (PK) of CSL889 (human hemopexin) when given intravenously (IV) to adults and adolescents with sickle cell disease (SCD) experiencing vaso-occlusive crises (VOC). The main objectives of the study are to evaluate the safety and tolerability of CSL889 in study participants, and to assess how CSL889 affects the time it takes for VOC to resolve in participants with SCD.
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Number of participants with treatment-emergent adverse events (TEAEs)
Timeframe: Up to Day 28 (End of study [EOS] Visit)
Percentage of participants with TEAEs
Timeframe: Up to Day 28 (EOS Visit)
Number of participants with detectable treatment emergent (TE) anti-CSL889 antibodies
Timeframe: Up to Day 28 (EOS Visit)
Percentage of participants with detectable TE anti-CSL889 antibodies
Timeframe: Up to Day 28 (EOS Visit)
Time to resolution of VOC (time to discontinuation of parenteral opioids)
Timeframe: Up to Day 28 (EOS Visit)