CHMP recommends approval of MenQuadfi for active immunisation of individuals from the age of 12 months and older against invasive meningococcal ACWY disease

22 September 2020 - Positive opinion based on a large, international clinical program demonstrating a good safety profile and a high ...

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CHMP recommends approval of Supemtek (quadrivalent recombinant influenza vaccine) for the prevention of influenza in adults aged 18 years and older

22 September 2020 - Positive opinion based on clinical data demonstrating safety and efficacy of Supemtek for adults aged 18 and ...

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Australia commits $123 million to a worldwide vaccine distribution alliance

22 September 2020 - Australia has committed $123 million to a worldwide vaccine distribution alliance, opening up the opportunity to ...

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Taking steps toward transparency in real world evidence studies

22 September 2020 - The level of trust in health economics and outcomes research studies has been an on-going concern owing ...

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Hikma updates on ANDA for generic Advair Diskus

22 September 2020 - Hikma Pharmaceuticals announces that it has received a minor complete response letter from the US FDA ...

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Medeor Therapeutics’ transplant immune tolerance therapy receives regenerative medicine advanced therapy designation from FDA

22 September 2020 - Medeor Therapeutics today announced that the U.S. FDA has granted a regenerative medicine advanced therapy designation ...

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U.S. FDA accepts for priority review Bristol Myers Squibb and bluebird bio application for anti-BCMA CAR T-cell therapy idecabtagene vicleucel (Ide-cel, bb2121)

22 September 2020 - Ide-cel is the first CAR T cell therapy accepted for regulatory review for multiple myeloma. ...

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Sanofi and GSK sign agreements with the Government of Canada to supply up to 72 million doses of adjuvanted COVID-19 vaccine

22 September 2020 - Agreements relate to vaccine candidate using Sanofi’s recombinant protein-based technology and GSK’s pandemic adjuvant. ...

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FDA launches the Digital Health Center of Excellence

22 September 2020 - Today, the U.S. Food and Drug Administration announced it is launching the Digital Health Center of Excellence ...

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Gyroscope Therapeutics granted FDA fast track designation for GT005, an investigational gene therapy for dry age-related macular degeneration

22 September 2020 - Gyroscope Therapeutics today announced that the U.S. FDA has granted fast track designation to GT005 for the ...

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ADC Therapeutics submits biologics license application to the U.S. FDA for loncastuximab tesirine for treatment of relapsed or refractory diffuse large B-cell lymphoma

21 September 2020 - Submission based on efficacy and safety data from LOTIS 2 clinical trial. ...

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CHMP grants positive opinion for expanded use of Otsuka’s Deltyba (delamanid) in children and adolescents weighing at least 30 kg treated for pulmonary multi-drug resistant tuberculosis

21 September 2020 - This label extension of Deltyba (delamanid) represents a new treatment option for children and adolescents with pulmonary ...

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Health Canada approves Inrebic (fedratinib), first new treatment in nearly a decade for patients living with myelofibrosis

21 September 2020 - Inrebic provides new, once-daily oral option for patients affected by rare bone marrow cancer. ...

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Knight and TherapeuticsMD announce Health Canada approval of Bijuva

21 September 2020 -  Knight Therapeutics and TherapeuticsMD announced today the approval of Bijuva (estradiol and progesterone) capsules by Health ...

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New early scientific advice service to support medicine registrations

22 September 2020 - The Therapeutic Goods Administration has launched a new initiative - the Early Scientific Advice service - ...

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