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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AbbVie receives a positive reimbursement recommendation from the Canadian Agencies for Drugs and Technology in Health (CADTH) pan-Canadian Oncology Drug Review Expert Review Committee (pERC) for Venclexta (venetoclax) in combination with azacitidine for acute myeloid leukaemia patients

26 August 2021 - pERC recommends reimbursement of Venclexta (venetoclax) in combination with azacitidine for the treatment of newly diagnosed acute ...

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Government eases criteria for haemophilia A drug reimbursement

26 August 2021 - The Government said it would ease the immune tolerance induction treatment criteria for haemophilia A drug ...

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Here’s how pharmacies set drug prices, and what consumers can do to save money

26 August 2021 - Americans are having a tough time paying for medications despite bipartisan efforts to drive down prescription ...

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ICER to assess treatments for COVID-19

26 August 2021 - Report will be subject of Midwest CEPAC meeting in April 2022; Draft Scoping Document open to public ...

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Moderna completes submission of biologics license application to the US FDA for its COVID-19 vaccine

25 August 2021 - Final blinded analysis of Phase 3 COVE study of the Moderna COVID-19 vaccine shows 93% efficacy; ...

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Ironwood Pharmaceuticals announces FDA approval of revised Linzess (linaclotide) label

26 August 2021 - Ironwood Pharmaceuticals today announced that the U.S. FDA approved a revised label for Linzess (linaclotide) based ...

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Sesen Bio pulls E.U. application for FDA rejected cancer drug

26 August 2021 - Sesen Bio, a small biotech firm whose investigational cancer treatment once seemed poised for approval, said ...

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Servier announces FDA approval of Tibsovo (ivosidenib tablets) in IDH mutated cholangiocarcinoma

25 August 2021 - TIBSOVO is the first and only targeted therapy approved for patients with previously treated IDH1-mutated cholangiocarcinoma. ...

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CellMax Life earns FDA breakthrough device designation for colon cancer & pre-cancerous adenomas screening blood test

25 August 2021 - FirstSight now qualifies for expedited FDA review process as a blood test for detection of advanced neoplasia ...

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Forxiga approved in Japan for the treatment of chronic kidney disease in patients with and without type 2 diabetes

26 August 2021 - Approval marks an important transformation in the treatment of more than 13 million people suffering from ...

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COVID-19 vaccine weekly safety report (26 August 2021)

26 August 2021 - To 22 August 2021, approximately 17.1 million vaccine doses have been given in Australia – 10.9 million ...

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Pfizer and BioNTech initiate rolling submission of supplemental biologics license application to U.S. FDA for booster dose of Comirnaty in individuals 16 and older

25 August 2021 - New Phase 3 data show booster (third) dose of Comirnaty induces significant SARS-CoV-2 neutralising antibody titres and ...

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PHARMAC seeks feedback on a biosimilar brand of adalimumab being considered for funding

26 August 2021 - PHARMAC is considering awarding Principal Supply to a biosimilar brand of adalimumab (Amgevita) from 1 February ...

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Vertex Pharma gets approval for cystic fibrosis drug for infants in Canada

25 August 2021 - Vertex Pharmaceuticals  was given approval to market its drug ivacaftor that treats children as young as ...

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Don’t meddle with Medicare to save a budget

25 August 2021 - House Democrats this week approved a $3.5 trillion budget framework that has already passed the Senate.  ...

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