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

+0.22%

Bristol-Myers Squibb Company

BMY

59.08

+0.22%

Feb 17 (Reuters) - 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

Further company coverage: BMY.N

More This page is machine-translated. Sahm tries to improve but does not guarantee the accuracy and reliability of the translation, and will not be liable for any loss or damage caused by any inaccuracy or omission of the translation. *Disclaimer: The above content only represents the author's personal position and opinion and does not represent any position of Sahm Capital Financial Company and Sahm cannot confirm the authenticity, accuracy, and originality of the above content. Investors should consider the risks of investment products in light of their circumstances before making any investment decisions. When necessary, please consult a professional investment advisor. Sahm does not provide any investment advice, nor does it make any commitments and guarantees.