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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New and amended PBS listings to help thousands of Australians

30 October 2021 - From 1 November 2021, Australians with a respiratory illness, early onset puberty and blood cancer will have ...

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PHARMAC negotiates deal for a further COVID-19 treatment

31 October 2021 - PHARMAC has negotiated an agreement with Roche to purchase another COVID-19 treatment.  ...

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FDA authorises Pfizer-BioNTech COVID-19 vaccine for emergency use in children 5 through 11 years of age

29 October 2021 - Today, the U.S. FDA authorised the emergency use of the Pfizer-BioNTech COVID-19 Vaccine for the prevention of ...

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U.S. Food and Drug Administration Approves Vuity (pilocarpine hydrochloride 1.25% ophthalmic solution) the first and only eye drop to treat presbyopia (age related blurry near vision)

29 October 2021 - Presbyopia, or age related blurry near vision, is a common, progressive condition that reduces the eye's ability ...

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Novartis UK awarded Innovation Passport for investigational therapy

29 October 2021 - Novartis have announced that the investigational oral therapy, iptacopan (LNP023), has been awarded an Innovation Passport ...

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FDA approves Novartis Scemblix (asciminib) with novel mechanism of action for the treatment of chronic myeloid leukemia

29 October 2021 - Scemblix provides much-needed and long-awaited new option for patients with chronic myeloid leukaemia who suffer with intolerance ...

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Kite's Tecartus (brexucabtagene autoleucel) authorised by Health Canada for the treatment of relapsed or refractory mantle cell lymphoma

28 October 2021 - Tecartus is first CAR T therapy in mantle cell lymphoma and Kite becomes the first company ...

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Public Summary Documents – July 2021 PBAC meeting

29 October 2021 - The public summary documents (positive recommendations and subsequent decisions not to recommend) from the July 2021 PBAC ...

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Incyte announces the validation of the European marketing authorisation application for ruxolitinib cream in vitiligo

28 October 2021 - The marketing authorisation application seeks approval of ruxolitinib cream for the treatment of adolescent and adult patients ...

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Reata Pharmaceuticals submits marketing authorisation application to the EMA for bardoxolone methyl in chronic kidney disease caused by Alport syndrome

28 October 2021 - Reata Pharmaceuticals today announced its submission of a marketing authorisation application for bardoxolone methyl to the ...

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CytoDyn announces FDA accepts revised rolling review timeline for resubmission of its BLA

28 October 2021 - Management expects the non-clinical and CMC sections of the BLA to be resubmitted to FDA in ...

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PBS arrangements for tocilizumab shortage – 1 November 2021

29 October 2021 - In response to the shortages of multiple presentations of tocilizumab (Actemra) products, the PBAC has recommended temporary ...

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NICE publishes final guidance for Janssen's apalutamide

28 October 2021 -  Final guidance for two indications. ...

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FDA acknowledges hurdles in utilising real world data

28 October 2021 - FDA is seeking to address the added complexities for incorporating real-world data and real-world evidence into ...

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Biden abandons his push to lower drug prices

28 October 2021 - The White House is abandoning every single policy idea aimed at lowering prescription drug prices in ...

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