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Maroc Maroc - DRUGS.COM - Daily MedNews - 06/Mar 21:06

FDA Approves TNKase for Acute Ischemic Stroke

THURSDAY, March 6, 2025 -- The U.S. Food and Drug Administration has approved TNKase (tenecteplase), a thrombolytic or clot-dissolving agent, for the treatment of acute ischemic stroke in adults.TNKase is delivered as a single five-second...

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FDA Approves TNKase (tenecteplase) for the Treatment of Acute Ischemic Stroke in Adults

drugs.com - 03/Mar 22:03

South San Francisco, CA -- March 3, 2025 -- Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced that the U.S. Food...

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FDA Approves Encelto (revakinagene taroretcel-lwey) for the Treatment of Macular Telangiectasia Type 2 (MacTel)

drugs.com - 06/Mar 22:03

CUMBERLAND, R.I.--(BUSINESS WIRE)--Neurotech Pharmaceuticals, Inc., a private biotech company focused on developing transformative therapies for...

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FDA Approves Stoboclo (denosumab-bmwo), a Biosimilar to Prolia

drugs.com - 03/Mar 00:03

JERSEY CITY, N.J., March 3, 2025 /PRNewswire/ -- Celltrion today announced that the U.S. Food and Drug Administration (FDA) has approved Stoboclo...

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FDA Approves Osenvelt (denosumab-bmwo), a Biosimilar to Xgeva

drugs.com - 03/Mar 00:03

JERSEY CITY, N.J., March 3, 2025 /PRNewswire/ -- Celltrion today announced that the U.S. Food and Drug Administration (FDA) has approved Osenvelt...

FDA approves treosulfan with fludarabine as a preparative regimen for alloHSCT in adult and paediatric patients with AML or MDS

oncologynews.com.au - 23/Feb 15:06

On January 21, 2025, the Food and Drug Administration approved treosulfan, an alkylating agent, with fludarabine as a preparative regimen for...

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FDA Approves Omlyclo (omalizumab-igec), an Interchangeable Biosimilar to Xolair

drugs.com - 07/Mar 22:03

March 07, 2025 -- Today, the U.S. Food and Drug Administration approved as the first interchangeable biosimilar to Xolair (omalizumab). Omlyclo, like...

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FDA Approves Odactra for the Treatment of House Dust Mite Allergy in Young Children

drugs.com - 28/Feb 23:02

February 27, 2025 -- ALK (ALKB:DC / OMX: ALK B) today announced that the US Food and Drug Administration (FDA) has approved ALK’s Odactra tablet...

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Indivior Announces FDA Approval of Label Changes for Sublocade (buprenorphine extended-release) Injection

drugs.com - 24/Feb 23:02

Richmond, VA, February 24, 2025 – Indivior PLC (Nasdaq/LSE: INDV), a global leader in addiction treatment, today announced that the U.S. Food...

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FDA Expands Indication of Dust Mite Allergy Drug to Include Young Children

drugs.com - 05/Mar 22:08

WEDNESDAY, March 5, 2025 -- The U.S. Food and Drug Administration has expanded its indication of Odactra, a house dust mite allergen tablet, for the...

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US FDA grants fast track designation to Latigo Biotherapeutics' LTG─001, an oral, investigational selective Nav1.8 inhibitor for the treatment of acute pain

pharmabiz.com - 04/Mar 23:54

Latigo Biotherapeutics (Latigo), a private clinical─stage biotechnology company, announced the US Food and Drug Administration (FDA) has granted...