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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Vaccinations can end political blame game: CSL

13 October 2021 - CSL chief Paul Perreault has warned that the politicisation of Covid-19 is ­fuelling vaccination hesitancy as ...

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DoH revises agenda ahead of new month's PBAC meeting

12 October 2021 - One minor change. ...

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EMA publishes agenda for 11-14 October CHMP meeting

11 October 2021 - The EMA has published a draft agenda for this week's CHMP meeting. ...

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Y-mAbs’ 177Lu-omburtamab-DTPA for the treatment of patients with medulloblastoma granted rare paediatric disease designation by FDA

7 October 2021 - Y-mAbs Therapeutics today announced that the U.S. FDA has granted rare paediatric disease designation for the Company’s ...

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EMA ends rolling review of CVnCoV COVID-19 vaccine following withdrawal by CureVac

13 October 2021 - The EMA has ended the rolling review of CVnCoV, CureVac AG’s COVID-19 vaccine, after the company ...

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GenSight Biologics announces FDA grant of fast track designation for optogenetic therapy GS030 as treatment for retinitis pigmentosa

12 October 2021 - GenSight Biologics today announced that the U.S. FDA has granted fast track designation to GS030, which combines ...

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Quanterix granted breakthrough device designation from U.S. FDA for blood based pTau 181 assay for Alzheimer’s disease

11 October 2021 - Quanterix Corporation announced today that its Simoa phospho-Tau 181 (pTau-181) blood test has been granted breakthrough ...

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SMC - October 2021 decisions

11 October 2021 - The Scottish Medicines Consortium, which advises on newly licensed medicines for use by NHSScotland has today ...

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Paying for cancer drugs that prove their benefit

11 October 2021 - The United States pays prices for brand name drugs that are estimated to be 256% higher than ...

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Health economic assessment of Poteligeo in the treatment of mycosis fungoides or Sézary syndrome

11 October 2021 - TLV has produced a health economic assessment for the regions for the drug Poteligeo (mogamulizumab).  ...

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Merck and Ridgeback announce submission of emergency use authorisation application to the U.S. FDA for molnupiravir, an investigational oral anti-viral medicine, for the treatment of mild to moderate COVID-19 in at risk adults

11 October 2021 - Submissions to regulatory agencies worldwide underway. ...

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Consternation as NICE rejects Janssen MS drug Ponvory

8 October 2021 - NICE has delivered its first verdict on NHS funding of Janssen’s oral multiple sclerosis drug Ponvory, ...

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Takeda's ovarian cancer drug Zejula gets expanded insurance benefit

1 October 2021 - Takeda Korea said its ovarian cancer treatment Zejula would receive expanded health insurance coverage as maintenance ...

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Tegsedi receives innovative drug category pricing in Brazil

11 October 2021 - PTC Therapeutics today announced that Tegsedi (inotersen) has successfully received Category 1 classification from Câmara de ...

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Medicare drug pricing debate pits savings against innovation

11 October 2021 - Proposal to allow Medicare to negotiate for lower prescription drug prices is central to Democrats’ health care, ...

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