AskBio receives FDA fast track designation for AB-1002 investigational gene therapy program in congestive heart failure

18 April 2024 - AB-1002 is being studied for the treatment of adults with non-ischaemic cardiomyopathy and New York Heart Association ...

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FDA approves Genentech's Alecensa as first adjuvant treatment for people with ALK positive early stage lung cancer

18 April 2024 - Approval based on Phase 3 ALINA study showing Alecensa reduced the risk of disease recurrence or death ...

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Alvotech and Teva announce US FDA Approval of Selarsdi (ustekinumab-aekn), biosimilar to Stelara (ustekinumab)

16 April 2024 - Selarsdi is expected to be marketed in the US on or after 21 February 2025, following a ...

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Lexeo Therapeutics granted FDA fast track designation for LX2006, an AAV based gene therapy candidate for the treatment of Friedreich’s ataxia cardiomyopathy

16 April 2024 - Lexeo Therapeutics today announced the US FDA has granted fast track designation to LX2006, the company’s AAVrh.10hFXN ...

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GSK’s 5 in 1 meningococcal ABCWY vaccine candidate accepted for regulatory review by US FDA

16 April 2024 - Submission based on results from pivotal Phase III trial showing all primary outcomes met. ...

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TLX101-CDx (Pixclara) granted FDA fast track designation

16 April 2024 - Telix Pharmaceuticals today announces that the US FDA has granted fast track designation for the Company's investigational ...

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PureTech receives FDA fast track designation for LYT-200 in head and neck cancers

11 April 2024 - LYT-200 is being evaluated in locally advanced/metastatic solid tumours, including head and neck cancers, as well as ...

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Fasenra approved for treatment of children aged 6 to 11 with severe asthma

11 April 2024 - AstraZeneca’s Fasenra (benralizumab) is now approved by the US FDA for add-on maintenance treatment for patients ...

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AdrenoMed receives FDA fast track designation for enibarcimab for treatment of septic shock

10 April 2024 - AdrenoMed today announced that the US FDA has granted fast track designation to its lead product candidate ...

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FDA accepts filing of new drug application for nalmefene auto-injector for the treatment of known or suspected opioid overdose

8 April 2024 - Purdue Pharma announced today that FDA has accepted for filing the company’s new drug application for the ...

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Lundbeck and Otsuka submit sNDA for FDA review of brexpiprazole and sertraline combination as potential treatment for PTSD

9 April 2024 - Lundbeck and Otsuka have submitted a supplemental new drug application for US FDA review of brexpiprazole ...

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Syros receives fast track designation from the FDA for tamibarotene for the treatment of newly diagnosed unfit AML with RARA gene over-expression

9 April 2024 - Syros Pharmaceuticals today announced that the US FDA has granted fast track designation to tamibarotene in ...

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ViiV Healthcare announces US FDA approval of Dovato (dolutegravir/lamivudine) for adolescents living with HIV

8 April 2024 - Dovato is now the first and only oral, two drug, single-tablet regimen available for people aged 12 ...

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Shorla Oncology announces FDA filing acceptance of new drug application to treat certain forms of leukaemia and other cancers

8 April 2024 - Second FDA acceptance for an NDA filing by Shorla Oncology announced in 2024. ...

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Supernus provides regulatory update for SPN-830

8 April 2024 - Supernus Pharmaceuticals today announced a regulatory update for SPN-830. ...

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