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Maroc Maroc - ZACKS.COM - All Stories - 05/Jul 12:59

Roche (RHHBY) Receives FDA Nod for Vabysmo Prefilled Syringe

The FDA approves Roche's (RHHBY) Vabysmo prefilled syringe for treating three retinal conditions that can cause blindness.

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FDA Approves Nemluvio for Prurigo Nodularis

drugs.com - 15/Aug 22:00

THURSDAY, Aug. 15, 2024 -- The U.S. Food and Drug Administration has approved Nemluvio (nemolizumab) for adult patients living with prurigo...

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Ascendis (ASND) Up on FDA Nod for Hormone Therapy Yorvipath

zacks.com - 14/Aug 16:31

The FDA approves Ascendis' (ASND) Yorvipath (palopegteriparatide) as the first and only treatment for hypoparathyroidism in adult patients. Shares...

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Treating and Preventing Bumblefoot in Chickens: A Comprehensive Guide

farmerstrend.co.ke - 14/Aug 19:40

Bumblefoot, scientifically known as pododermatitis, is a common, painful yet serious bacterial infection that affects the feet of chickens. This...

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What is mpox? How does it spread and can it be treated?

asianewsday.com - 14/Aug 18:53

NEW YORK – The global eradication of smallpox more than 40 years ago was one of the greatest achievements in public health history, vanquishing a...

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Gilead (GILD) Obtains FDA Approval for PBC Drug Livdelzi

zacks.com - 17/Aug 05:44

Gilead (GILD) wins FDA nod for seladelpar for the treatment of primary biliary cholangitis (PBC) on an accelerated basis.

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FDA Approves Nemluvio (nemolizumab) for the Treatment of Adult Patients with Prurigo Nodularis

drugs.com - 13/Aug 21:08

Zug, Switzerland – August 13, 2024 – Galderma today announced that the U.S. Food and Drug Administration (FDA) has approved Nemluvio...

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FDA Approves Yorvipath (palopegteriparatide) for the Treatment of Hypoparathyroidism in Adults

drugs.com - 12/Aug 19:08

COPENHAGEN, Denmark, Aug. 12, 2024 (GLOBE NEWSWIRE) -- Ascendis Pharma A/S (Nasdaq: ASND) today announced that the U.S. Food & Drug Administration...

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FDA Approves Rybrevant (amivantamab-vmjw) Plus Lazcluze (lazertinib) for Patients with EGFR-Mutated Advanced Lung cancer

drugs.com - 20/Aug 21:08

RARITAN, N.J., Aug. 20, 2024 /PRNewswire/ -- Johnson & Johnson (NYSE: JNJ) announced today that the U.S. Food and Drug Administration (FDA)...

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FDA Approves Lymphir (denileukin diftitox-cxdl) Immunotherapy for the Treatment of Adults with Relapsed or Refractory Cutaneous T-Cell Lymphoma

drugs.com - 08/Aug 22:08

CRANFORD, N.J., Aug. 8, 2024 /PRNewswire/ -- Citius Pharmaceuticals, Inc. (NASDAQ: CTXR) ("Citius", "Citius Pharma"), announced today that the U.S....