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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Roche launches cobas PIK3CA mutation test for patients with advanced or metastatic breast cancer in countries accepting the CE mark

15 December 2020 - This genetic test identifies mutations in the PIK3CA gene that can cause cells to grow uncontrollably, which ...

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New criteria changes who’ll get COVID-19 vaccine first

16 December 2020 - Australia’s population is expected to be divided into 12 age brackets for the much-anticipated rollout of ...

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Vaccination strategy against SARS-Cov-2

15 December 2020 - Intermediate recommendations on the methods of implementing vaccination. ...

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Big Pharma’s new CEOs must step up to erase inequities in drug access

16 December 2020 - I have been asked many times: Does the vision of the CEO have the power to ...

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FDA committee to meet again Thursday for Moderna's COVID-19 vaccine

14 December 2020 - A Food and Drug Administration advisory committee will meet for the second time in a week to ...

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Trump’s plan for $200 Medicare drug cards advances, though hurdles remain

15 December 2020 - An industry group that ensures standards are met for health-benefit cards gave its approval for the $200 ...

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Rafael Pharmaceuticals receives FDA fast track designation for CPI-613 (devimistat) for the treatment of acute myeloid leukaemia

15 December 2020 - Rafael Pharmaceuticals announced today that the U.S. FDA has granted fast track designation for the Company’s ...

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U.S. FDA accepts new drug application for review, grants priority review for Takeda’s TAK-721 (budesonide oral suspension) for the treatment of eosinophilic oesophagitis

15 December 2020 - If approved, TAK-721 will be the first FDA approved treatment for the chronic inflammatory disease; Takeda plans ...

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FDA awards Genetesis breakthrough device designation for CardioFlux imaging technology

15 December 2020 - Genetesis announced today that its flagship product, CardioFlux, has been granted Breakthrough Device Designation by the U.S. ...

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Update on assessment of the BioNTech and Pfizer BNT162b2 vaccine marketing authorisation application

15 December 2020 - EMA’s CHMP and its experts have been working intensively over the past weeks to evaluate data ...

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28 state Attorneys General demand HHS Secretary Azar enforce laws on 340B drug pricing

14 December 2020 - AIDS Healthcare Foundation praised 28 U.S. state attorneys general who have drawn a line in the sand ...

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Almirall announces FDA approval of Klisyri (tirbanibulin), a new innovative topical treatment for actinic keratosis

15 December 2020 - In one of the largest Phase 3 clinical trial programs ever conducted for a topical actinic keratosis ...

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Imfinzi recommended for approval in the EU by CHMP for less-frequent, fixed-dose use in unresectable non-small cell lung cancer

15 December 2020 - Option would extend dosing from two to four weeks, reducing medical visits and improving patient convenience ...

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European CHMP adopts positive opinion for Heplisav-B, Dynavax's two dose adult hepatitis B adjuvanted vaccine

10 December 2020 - If approved, Heplisav-B will be the only two dose adult hepatitis B vaccine offering protection in just ...

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'Digital contraceptive' gets approval by Australian health authorities

15 December 2020 - A smartphone app can officially be used as a contraceptive tool by Australians after becoming the ...

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