On Thursday, the U.S. Food and Drug Administration (FDA) approved Journavx (suzetrigine) 50 mg oral tablets, a first-in-class non-opioid analgesic for...
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Maroc - DRUGS.COM - Pharma Industry News - 05/Jan 22:53
MONDAY, Jan. 5, 2026 -- The U.S. Food and Drug Administration has approved Myqorzo (aficamten) for the treatment of adults with symptomatic obstructive hypertrophic cardiomyopathy (oHCM).Myqorzo is a cardiac myosin inhibitor that directly addresses...
On Thursday, the U.S. Food and Drug Administration (FDA) approved Journavx (suzetrigine) 50 mg oral tablets, a first-in-class non-opioid analgesic for...
On Thursday, the U.S. Food and Drug Administration (FDA) approved Journavx (suzetrigine) 50 mg oral tablets, a first-in-class non-opioid analgesic for...
January 12, 2026 -- The U.S. Food and Drug Administration today approved the Zycubo (copper histidinate) injection as the first treatment for Menkes...
January 12, 2026 -- The U.S. Food and Drug Administration today approved the Zycubo (copper histidinate) injection as the first treatment for Menkes...
LUND, Sweden, Jan. 9, 2026 /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that the U.S. Food and Drug Administration (FDA) has accepted...
LUND, Sweden, Jan. 9, 2026 /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that the U.S. Food and Drug Administration (FDA) has accepted...
TUESDAY, Jan. 20, 2026 — A U.S. Food and Drug Administration (FDA)-approved device for treating ADHD in kids simply doesn’t work, a new...
TUESDAY, Jan. 20, 2026 — A U.S. Food and Drug Administration (FDA)-approved device for treating ADHD in kids simply doesn’t work, a new...
FDA approves Mitapivat, the first oral treatment for thalassemia anemia, helping reduce transfusion needs and raise hemoglobin levels in adults.
THURSDAY, Jan. 8, 2026 — The U.S. Food and Drug Administration (FDA) has again missed a deadline to propose a ban on chemicals in...