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The first new drug to treat amyotrophic lateral sclerosis in more than 20 years has been approved by the U.S. Food and Drug Administration.

FDA Approves Radicava for Amyotrophic Lateral Sclerosis

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Radicava, given intravenously, slows physical decline in patients with ALS
Brineura (cerliponase alfa) has been approved by the U.S. Food and Drug Administration to treat a specific form of Batten disease

Enzyme Replacement Drug OK’d for Form of Batten Disease

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Brineura will be used to treat children with late infantile neuronal ceroid lipofuscinosis type 2 Batten
Rydapt (midostaurin) has been approved by the U.S. Food and Drug Administration

FDA Approves Kinase Inhibitor for Treatment of AML

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Midostaurin, in combination with chemotherapy, treats acute myeloid leukemia in adults
U.S. Food and Drug Administration approval of the kinase inhibitor regorafenib has been expanded to include hepatocellular carcinoma

Regorafenib Approved for Hepatocellular Carcinoma

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It is the first approved treatment for HCC in almost a decade
A new noninvasive device

FDA OKs Vagus Nerve Stimulator to Treat Cluster Headaches

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Hand-held, noninvasive device provides new option
Ingrezza (valbenazine)

FDA Approves First Drug for Treatment of Tardive Dyskinesia

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Ingrezza (valbenazine) capsules approved for treatment of adults with tardive dyskinesia
Dupixent (dupilumab) has been approved by the U.S. Food and Drug Administration to treat moderate-to-severe eczema that isn't well controlled by topical medication.

FDA Approves Dupixent to Treat Eczema

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Active ingredient binds to protein (interleukin-4 receptor alpha subunit) that causes inflammation
The intravenous drug Ocrevus (ocrelizumab) has been approved by the U.S. Food and Drug Administration to treat adults with primary progressive multiple sclerosis and relapsing forms of the disease

FDA Approves Ocrevus to Treat Severe Form of Multiple Sclerosis

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First drug sanctioned in United States for primary progressive multiple sclerosis
Zejula (niraparib) has been approved by the U.S. Food and Drug Administration to treat adult women with recurrent epithelial ovarian

FDA Approves Zejula for Certain Female Cancers

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PARP inhibitor may help fight tumors affecting the ovaries, fallopian tubes, or peritoneum
Bavencio (avelumab) has been approved by the U.S. Food and Drug Administration to treat Merkel cell carcinoma

FDA Approves Bavencio for Merkel Cell Carcinoma

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Drug targets the PD-1/PD-L1 pathway; first sanctioned treatment in the United States