FDA approval of Leqembi subcutaneous formulation charts path to combination therapies for Alzheimer's disease

29 August 2025 - Subcutaneous delivery increases accessibility and introduces potential for at home administration, following model of diabetes and ...

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Political preoccupation with prescription drug costs may distract from larger problem of hospital costs

2 September 2021 - It’s no secret that per capita health care costs are very high in the U.S. This wouldn’t ...

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Natco Pharma (Canada) announces the launch of Nat-Lenalidomide capsules, the first generic alternative to Revlimid

1 September 2021 - Nat-Lenalidomide expands affordable treatment options for patients with multiple myeloma and patients with transfusion-dependent anaemia due to ...

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FDA to hold Advisory Committee meeting to discuss Pfizer-BioNTech’s application for COVID-19 booster

2 September 2021 - Today, the U.S. FDA announced a virtual meeting of its Vaccines and Related Biological Products Advisory ...

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CAR-T therapy Kymriah fails to get insurance benefits

2 September 2021 - The first CAR-T therapy, Kymriah (ingredient: tisagenlecleucel), failed to pass the review of a panel at ...

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ECDC and EMA highlight considerations for additional and booster doses of COVID-19 vaccines

2 September 2021 - Based on current evidence, there is no urgent need for the administration of booster doses of vaccines ...

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Moderna announces submission of initial data to US FDA for its COVID-19 vaccine booster

1 September 2021 - mRNA-1273 at 50 µg dose level induced robust antibody responses of more than 40x against the ...

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Updated agenda for the November 2021 PBAC meeting

2 September 2021 - The agenda for the November 2021 PBAC meeting has been updated.  ...

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COVID-19 vaccine weekly safety report (2 September 2021)

2 September 2021 - To 29 August 2021, over 19 million vaccine doses have been given in Australia – approximately 12 ...

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Coherus and Junshi Biosciences announce completion of rolling BLA submission to U.S. FDA for toripalimab for the treatment of nasopharyngeal carcinoma

1 September 2021 - Junshi Biosciences and Coherus Biosciences announced today the completion of the rolling submission of the biologics ...

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FDA approves zanubrutinib for Waldenström’s macroglobulinaemia

1 September 2021 - On 31 August 2021, the Food and Drug Administration approved zanubrutinib (Brukinsa, BeiGene) for adult patients with ...

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In2Bones receives FDA clearance for pre-surgery OrthoPlanify patient specific planning software and 3D printed cutting guides for Quantum Total Ankle System

1 September 2021 - In2Bones Global today announces the FDA clearance of OrthoPlanify patient-specific planning software and 3D printed cutting ...

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Intelivation Technologies received FDA approval for the Golden Isles Pedicle Screw System

1 September 2021 - Intelivation Technologies announced today that they have achieved FDA 510(k) Clearance of the Golden Isles Pedicle ...

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FDA requires warnings about increased risk of serious heart related events, cancer, blood clots, and death for JAK inhibitors that treat certain chronic inflammatory conditions

1 September 2021 - Based on a completed U.S. FDA review of a large randomised safety clinical trial, we have concluded ...

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FDA approves drug for schizophrenia to be administered at a six month interval

1 September 2021 - The FDA has approved Invega Hafyera (paliperidone palmitate) extended-release injectable suspension to treat schizophrenia in certain ...

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U.S. FDA grants breakthrough device designation for innovative EndoSound vision ultrasound system

1 September 2021 - Endosound announced today that its EndoSound Vision System received a Breakthrough Device Designation from the U.S. FDA. ...

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