Bluebird Bio Decision in Europe Is A Wake-Up Call For Payers and Industry
Compromise On Prices Will Be Needed In The Future
Bluebird bio’s decision to focus on the US market is being seen as a broader signal of the need for changes in market access policies to enable gene therapies to be made available for European patients. Only collaborative work will create solutions acceptable to payers and companies, and finding an acceptable price that both can live with will be crucial.
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Gene Therapy: Bluebird’s Eli-Cel Efficacy Uncertain, Malignancy Risk Concerning, US FDA Says
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Gene Therapy Development Should Involve Fewer Surprises, Says US FDA’s Marks
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