0.8 kg in placebo over 24 weeks) that did not meet the magnitude needed for regulatory approval
However, if the FDA ultimately reclassifies them and they are produced by compounding pharmacies in the U.S., clinicians would have discretion to write prescriptions outside of those narrow indications
Munekage E, Takezaki Y, Hanazaki K
Yilmaz M, MD, Kantarjian H, MD, Short NJ, MD, Konopleva M, MD, PhD, Kadia TM, MD, DiNardo CD, MD, MSCE, Borthakur G, MD, Pemmaraju N, MD, Maiti A, MBBS, Jabbour EJ, MD, Issa GC, MD, Jain N, MD, Takahashi K, MD, PhD, Sasaki K, MD, PhD, Ohanian M, DO, Tang G, MD, PhD, Loghavi S, MD, Patel K, MD, PhD, Garcia-Manero G, MD, Andreeff M , MD, PhD, Ravandi F, MBBS, Daver N, MD

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