BRIEF-U.S. FDA Accepts Bristol Myers Squibb's NDA For Iberdomide In Multiple Myeloma

Bristol-Myers Squibb Company -0.33% Pre

Bristol-Myers Squibb Company

BMY

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- FDA:

  • U.S. FOOD AND DRUG ADMINISTRATION ACCEPTS BRISTOL MYERS SQUIBB'S NEW DRUG APPLICATION FOR IBERDOMIDE IN PATIENTS WITH RELAPSED OR REFRACTORY MULTIPLE MYELOMA

  • BRISTOL-MYERS SQUIBB CO: U.S. FDA ASSIGNS A TARGET ACTION DATE OF AUGUST 17, 2026, GRANTS BREAKTHROUGH THERAPY DESIGNATION & PRIORITY REVIEW

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