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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ICER identifies most significant 2019 US drug price hikes — even after rebates — that were not supported by new clinical evidence

12 January 2021 - Out of 10 identified drugs that had substantial 2019 price increases on top of already high current ...

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Vaccine ‘is not good enough’ to stop the virus

13 January 2021 - Doctors are calling for a re-evaluation of Australia’s vaccine strategy, saying that herd immunity cannot be ...

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Janssen's ulcerative colitis treatment to receive reimbursement

12 January 2021 - Janssen Pharmaceutical said Tuesday that the Ministry of Health and Welfare would begin to reimburse Stelara, ...

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EMA receives application for conditional marketing authorisation of COVID-19 Vaccine AstraZeneca

12 January 2020 - EMA has received an application for conditional marketing authorisation (CMA) for a COVID-19 vaccine developed by AstraZeneca ...

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Health Canada approves Bavencio for the maintenance treatment of patients with advanced bladder cancer

11 January 2021 - Bavencio is the first and only maintenance therapy for unresectable locally advanced or metastatic urothelial carcinoma ...

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Acrux receives FDA approval for its generic testosterone topical solution

12 January 2021 - Acrux is pleased to announce that the US FDA has approved its generic product based on ...

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From 1 February 2021 pre-COVID-19 Special Authority criteria will be reinstated

12 January 2020 - The temporary changes will remain in place for any Special Authority applications for the relevant medicines made ...

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ObsEva provides update on Yselty (linzagolix) clinical development program

11 January 2021 - European Medicines Agency validates Yselty marketing authorisation application for uterine fibroids; US NDA Planned for 1H 2021. ...

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Aerie Pharmaceuticals receives European Commission approval for Roclanda (netarsudil and latanoprost ophthalmic solution) 0.02%/0.005%

11 January 2021 - Aerie Pharmaceuticals today announced the European Commission has granted a marketing authorisation for Roclanda (netarsudil and latanoprost ...

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Decision to widen access to valganciclovir for transplant patients

12 January 2021 - PHARMAC is pleased to announce a decision to widen access to valganciclovir for use after lung ...

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Exicure granted two fast track designations for cavrotolimod (AST-008) from the U.S. Food and Drug Administration

11 January 2021 - Exicure today announced that the U.S. FDA has granted fast track designations for its clinical product ...

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Insights from the January 2021 issue of the Schedule of Pharmaceutical Benefits

12 January 2021 - The January 2021 issue of the Schedule of Pharmaceutical Benefits tells very different tales for two innovative ...

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Most Australians will get the AstraZeneca coronavirus vaccine, but priority groups will receive the Pfizer drug. What's the difference?

12 January 2021 - As Australians navigate lockdowns, border closures, hotel quarantine and COVID-19 testing queues, the wait for the ...

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Myriad Genetics receives first reimbursement decision for myChoice diagnostic system in Japan, enabling women with ovarian cancer to benefit from treatment with Zejula

8 January 2021 - Myriad Genetics announced today that it received its first reimbursement decision for the Myriad myChoice Diagnostic System, ...

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Democrats have their best shot yet at letting Medicare negotiate drug prices — but it’s still not a done deal

11 January 2021 - Democrats have their best shot in more than a decade to deliver on one of the ...

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