Axovant Gene Therapies receives rare paediatric disease designation for AXO-AAV-GM1 for GM1 gangliosidosis

9 October 2020 - Company on-track to report data from on-going Phase 1/2 clinical study in Q4 2020. ...

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Moderna vows to not enforce COVID-19 vaccine patents during pandemic

8 October 2020 - The company is also willing to license the technology behind its experimental coronavirus vaccine. ...

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Can Trump really speed approval of COVID treatments?

10 October 2020 - In a five minute video posted to his Twitter account on Wednesday, President Trump stood in ...

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Health Canada approves Inqovi (decitabine and cedazuridine) oral therapy for two types of blood cancers, MDS and CMML

8 October 2020 - Oral drug can be taken at home, which may enable some patients to avoid some hospital visits. ...

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Pfizer Canada and BioNTech initiate rolling submission to Health Canada for SARS-CoV-2 vaccine candidate BNT162b2

9 October 2020 - Pfizer Canada and BioNTech will continue regular and open dialogue with Health Canada providing results from their ...

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Italfarmaco receives FDA rare paediatric disease designation for givinostat in Duchenne muscular dystrophy, announces completed enrolment in EPIDYS Phase 3 trial

9 October 2020 - The Italfarmaco Group provided today an update on the development of givinostat, its proprietary histone deacetylase ...

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NDA filing for Luye Pharma’s anti-depressant drug LY03005 accepted by the U.S. FDA

4 March 2020 - Luye Pharma Group has announced that the U.S. FDA has reviewed and accepted the filing of ...

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New transparency measures for prescription medicines

9 October 2020 - The Australian Government has given approval to proceed with two measures to enhance transparency for prescription ...

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Eton Pharmaceuticals announces acceptance for filing of new drug application for orphan drug dehydrated alcohol injection

8 October 2020 - Application assigned a PDUFA date of 27 May 2021. ...

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MHRA to join Project Orbis

8 October 2020 - The UK is set to join the US FDA's Project Orbis at the start of next ...

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Johnson & Johnson announces European Commission approval of agreement to supply 200 million doses of Janssen’s COVID-19 vaccine candidate

8 October 2020 - Agreement provides option for European Union Member States to secure up to 200 million additional doses for ...

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BioMarin receives FDA approval of label expansion to allow maximum dose of 60 mg for Palynziq (pegvaliase-pqpz) injection for treatment of adults with PKU

7 October 2020 - New safety and efficacy data out to 3 years for first and only enzyme therapy to treat ...

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U.S. FDA grants rare paediatric disease designation to Cerecin’s investigational drug tricaprilin for the treatment of infantile spasms

8 October 2020 - Cerecin announced that the U.S. FDA has granted rare paediatric disease designation to tricaprilin, an investigational drug ...

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X4 Pharmaceuticals announces fast track designation granted by the FDA to mavorixafor for the treatment of WHIM syndrome

8 October 2020 - X4 Pharmaceuticals today announced that the U.S. FDA has granted fast track designation to its lead ...

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AstraZeneca vaccine document shows limit of no-profit pledge

8 October 2020 - Company has right under contract to declare pandemic over by July 2021. ...

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