Lexicon submits new drug application for sotagliflozin for the treatment of heart failure in adults with type 2 diabetes

30 December 2021 - ) -- Lexicon Pharmaceuticals today announced that it has submitted a new drug application to the U.S. ...

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Amylyx Pharmaceuticals announces FDA acceptance and priority review of new drug application for AMX0035 for the treatment of ALS

29 December 2021 - Amylyx Pharmaceuticals today announced that the U.S. FDA has accepted for review its new drug application for ...

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Janssen submits biologics license application to U.S. FDA seeking approval of teclistamab for the treatment of patients with relapsed or refractory multiple myeloma

29 December 2021 - Janssen  announced today the submission of a biologics license application to the U.S. FDA seeking approval ...

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Swiss regulator approves Roche-Regeneron COVID-19 drug

27 December 2021 - The Swiss medicines agency, Swissmedic, has given the green light to the monoclonal antibody cocktail Ronapreve developed ...

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Janssen COVID-19 booster shot approved in Switzerland

28 December 2021 - Medicines regulator Swissmedic has approved the booster of the single-dose vaccine from Johnson & Johnson. ...

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LEO Pharma announces FDA approval of Adbry (tralokinumab) as the first and only treatment specifically targeting IL-13 for adults with moderate to severe atopic dermatitis

28 December 2021 - Adbry is the first biologic launched by LEO Pharma in the United States and is expected to ...

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COVID-19 vaccine weekly safety report (23 December 2021)

23 December 2021 - To 19 December 2021, the TGA has received 415 reports which have been assessed as likely to ...

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Trastuzumab deruxtecan type II variation application validated by EMA for patients with HER2 positive metastatic breast cancer treated with a prior anti-HER2 based regimen

28 December 2021 - Application based on DESTINY-Breast03 results showing Daiichi Sankyo and AstraZeneca’s trastuzumab deruxtecan reduced risk of disease progression ...

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Vivoryon Therapeutics receives FDA fast track designation for varoglutamstat in early Alzheimer’s disease

22 December 2021 - 21 – Vivoryon Therapeutics today announced that the U.S. FDA has granted fast track designation for varoglutamstat ...

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Celularity receives fast track designation from U.S. FDA for its NK cell therapy CYNK-001 in development for the treatment of AML

27 December 2021 - Celularity today announced the U.S. FDA has granted fast track designation for its non-genetically modified cryopreserved human ...

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FDA approves add-on therapy to lower cholesterol among certain high-risk adults

22 December 2021 - FDA has approved Leqvio (inclisiran) injection as a treatment to be used along with diet and maximally ...

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Lion TCR receives FDA fast track designation for its HBV specific TCR T cell therapy for hepatocellular carcinoma

23 December 2021 - Lion TCR today announced that it has received fast track designation from U.S. FDA for LioCyx-M004, autologous ...

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Patritumab deruxtecan granted U.S. FDA breakthrough therapy designation in patients with metastatic EGFR mutated non-small-cell lung cancer

23 December 2021 - First breakthrough therapy designation for patritumab deruxtecan based on results of Phase 1 trial. ...

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Coherus announces U.S. FDA approval of Yusimry (adalimumab-aqvh)

20 December 2021 - Approved for all eligible indications of the reference biological product, Humira (adalimumab). ...

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Novartis Cosentyx receives FDA approval for the treatment of children and adolescents with enthesitis related arthritis and psoriatic arthritis

22 December 2021 - New approvals are based on JUNIPERA trial data showing Cosentyx (secukinumab) demonstrated reduced flare risk versus placebo ...

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