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EMA – New medicine for rare type of eye cancer

EMA has recommended granting a marketing authorisation in the European Union (EU) for Kimmtrak (tebentafusp), a monotherapy for the treatment of adult patients with...

FDA limits use of GlaxoSmithKline and Vir’s COVID-19 antibody treatment in some geographic areas

The United States Food and Drug Administration stated GlaxoSmithKline and Vir Biotech's COVID-19 antibody treatment should not be used in places with circulation...

Markus Soeder: Sputnik V vaccine project in Bavaria is closed

Bavaria will block the production of Russia's Sputnik COVID-19 vaccine even if it is approved by the European Medicines Agency, the premier of the...

Sanofi and GSK to seek regulatory authorization for COVID-19 vaccine

The French and British drugmakers Sanofi and GSK are ready to seek approval from regulators for their Covid-19 vaccine after reporting positive results from...

EU regulator approves Pfizer-BioNTech vaccine booster for ages 12 to 17

Pfizer Inc. and BioNTech announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) issued a positive...

EMA recommends approval of Spikevax for children aged 6 to 11

EMA’s human medicines committee (CHMP) has recommended granting an extension of indication for the COVID-19 vaccine Spikevax to include use in children aged 6...
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