Gilead’s magrolimab, an investigational anti-CD47 monoclonal antibody, receives FDA breakthrough therapy designation for treatment of myelodysplastic syndrome

15 September 2020 - On-going clinical program includes the Phase 3 ENHANCE trial in myelodysplastic syndrome. ...

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FDA publishes comparative performance data for COVID-19 molecular diagnostic tests

15 September 2020 - Today, the U.S. FDA published comparative performance data for some authorised COVID-19 molecular diagnostic tests.  ...

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Estimating risk ratios and risk differences: alternatives to odds ratios

15 September 2020 - The goal of many medical research studies is to estimate the direction and magnitude of the effect ...

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Rep Grothman introduces bill for automatic insulin biosimilar interchangeablity

15 September 2020 - Representative Glenn Grothman, (R-Wisconsin), says interchangeability for insulins makes sense based on the savings potential and safety ...

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NIH 'very concerned' about serious side effect in AstraZeneca coronavirus vaccine trial

15 September 2020 - The FDA is weighing whether to follow British regulators in resuming a coronavirus vaccine trial that ...

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Apellis announces submission of pegcetacoplan marketing applications to FDA and EMA for patients with PNH

15 September 2020 -  -- Apellis Pharmaceuticals today announced that the company has submitted a new drug application to the ...

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Plus Therapeutics receives fast track designation from FDA for its novel glioblastoma treatment

15 September 2020 - Plus Therapeutics today announced that the U.S. FDA has granted the Company fast track designation for its ...

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US FDA grants fast track designation to Jardiance (empagliflozin) to improve outcomes following a heart attack

15 September 2020 - This fast track designation for empagliflozin emphasises the urgent need for potential treatments that may improve outcomes ...

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Ziopharm Oncology granted rare paediatric disease designation for controlled IL-12 for the treatment of DIPG

14 September 2020 -  -- Ziopharm Oncology today announced that the U.S. FDA has granted rare paediatric disease designation to ...

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Vaccine makers keep safety details quiet, alarming scientists

13 September 2020 - Researchers say drug companies need to be more open about how vaccine trials are run to reassure ...

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ESSA Pharma announces fast track designation granted by the FDA to EPI-7386 for the treatment of metastatic castration-resistant prostate cancer

14 September 2020 - ESSA Pharma today announced that the US FDA granted fast track designation to EPI-7386, its oral ...

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Sol-Gel Technologies announces FDA acceptance for filing of new drug application for Epsolay for the treatment of inflammatory lesions of rosacea

10 September 2020 - Potential to be first FDA-approved single-agent benzoyl peroxide prescription drug product. ...

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Mallinckrodt receives a complete response letter from the U.S. FDA for terlipressin for the treatment of hepatorenal syndrome type 1

14 September 2020 - Company remains committed to working with FDA toward an approval for this important potential therapy. ...

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FDA grants Dupixent (dupilumab) breakthrough therapy designation for eosinophilic oesophagitis

14 September 2020 - There are currently no FDA approved treatments for this chronic type 2 inflammatory disease that damages the ...

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Pfizer CEO 'preparing' for likelihood of vaccine approval before end of year

13 September 2020 - Pharmaceutical company Pfizer is preparing for the likelihood of regulators approving the coronavirus vaccine the company ...

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