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U.S. Food and Drug Administration Accepts Bristol Myers Squibb's New Drug Application for Iberdomide in Patients with Relapsed or Refractory Multiple Myeloma

PRINCETON, N.J., February 17, 2026--U.S. Food and Drug Administration Accepts Bristol Myers Squibb's New Drug Application for Iberdomide in Relapsed or Refractory Multiple Myeloma

articleBristol-myers Squibb CompanyFebruary 17, 20264/company/bristol-myers-squibb-company/news/us-food-and-drug-administration-accepts-bristol-myers-squibbs-new-drug-application-for-iberdomide-in-patients-with-relapsed-or-refractory-multiple-myeloma
U.S. Food and Drug Administration Accepts Bristol Myers Squibb's New Drug Application for Iberdomide in Patients with Relapsed or Refractory Multiple Myeloma

About this update from Bristol-myers Squibb Company

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Bristol Myers Squibbmultiple myelomaNew Drug ApplicationFood and Drug AdministrationMRDpatientsprogression-free survivalminimal residual disease