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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EMA grants PRIME designation for JR-141 for the treatment of mucopolysaccharidosis type II (Hunter syndrome)

18 October 2021 - JCR Pharmaceuticals announced today that the EMA has granted PRIME designation for the investigational drug JR-141 (pabinafusp ...

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Australia secures additional COVID-19 treatments

17 October 2021 - The Australian Government has secured access to two additional COVID-19 treatments to support the National Plan to ...

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FDA approves naloxone injection to counteract opioid overdoses

18 October 2021 - The FDA has approved Zimhi (naloxone hydrochloride) injection as an additional option to treat opioid overdose. ...

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FDA approves Cyltezo, the first interchangeable biosimilar to Humira

18 October 2021 - The U.S. FDA approved the first interchangeable biosimilar product to treat certain inflammatory diseases. ...

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NICE approves Ofev for PF-ILD

18 October 2021 - NICE has recommended Boehringer Ingelheim’s Ofev (nintedanib) for the treatment of adult patients with chronic fibrosing ...

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New asthma drug approved on NHS branded a ‘wonder drug’

18 October 2021 - NICE has issued a Final Appraisal Determination recommending dupilumab as an add-on maintenance treatment for severe ...

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EMA starts evaluating use of COVID-19 vaccine Comirnaty in children aged 5 to 11

18 October 2021 - EMA has started evaluating an application to extend the use of BioNTech/Pfizer’s COVID-19 vaccine, Comirnaty, to ...

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Novartis applauds Quebec, the first province to list Zolgensma for the treatment of paediatric patients with spinal muscular atrophy

15 October 2021 - Public reimbursement under the Régie de l'assurance maladie du Québec, effective October 20th will apply for children ...

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TGA provisional approval of Roche COVID-19 treatment, casirivimab with imdevimab (Ronapreve)

18 October 2021 - The TGA has provisionally approved the use of the Roche combination therapy, casirivimab + imdevimab (Ronapreve) ...

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FDA needs a competitiveness czar

15 October 2021 - The FDA needs a Deputy Commissioner for Regulatory Competitiveness.  ...

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Recent trends in Medicaid spending and use of drugs with US Food and Drug Administration accelerated approval

8 October 2021 - In this cross-sectional study of 216 drugs granted accelerated approval from 1992 through 2020, relative to all ...

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How much does it cost to research and develop a new drug? A systematic review and assessment

15 October 2021 - Debate over the viability of the current commercial research and development model is on-going.  ...

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Recommendations made by the PBAC – September 2021 intracycle meeting

15 October 2021 - First PBAC recommendation for a new gene therapy. ...

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Pfizer’s abrocitinib receives positive CHMP opinion for the treatment of adults with moderate to severe atopic dermatitis

15 October 2021 - CHMP also recommends Xeljanz (tofacitinib) approval for the treatment of adults with active ankylosing spondylitis ...

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Merck and Eisai receive positive EU CHMP opinions for Keytruda (pembrolizumab) plus Lenvima (lenvatinib) in two different types of cancer

15 October 2021 - Merck and Eisai today announced that the CHMP of the EMA has adopted positive opinions recommending ...

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