bluebird bio’s plans to file for approval of lovotibeglogene autotemcel (lovo-cel) in severe sickle cell disease (SCD) in the first quarter of 2023 will no doubt ignite debate over its cost-effectiveness. A study presented at the American Society of Hematology annual meeting looked beyond traditional criteria for cost effectiveness, concluding that despite the gene therapy’s presumably high price tag, it could be an equitable therapeutic strategy in a wider pool of eligible patients.
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