News
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorisation for Amgen’s Tepezza ...
iOnctura has begun a randomized phase 1/2 study investigating its lead asset, roginolisib, in combination with dostarlimab, ...
UCB has announced that its developmental treatment DoxTM, a combination of doxecitine and doxribtimine, has been granted ...
Janssen-Cilag International NV, a Johnson & Johnson company, has submitted an application to the European Medicines Agency ...
The Americas Awards are excited to introduce a new category, Clinical Trial Administrator. This category is designed to ...
Chiesi UK and Ireland and Wirral Primary Care Collaborative (WPCC) have launched COMET, a programme designed to enhance early ...
Janssen-Cilag International NV, a Johnson & Johnson company, has submitted an application to the European Medicines Agency (EMA) to extend the marketing authorisation for RYBREVANT (amivantamab) with ...
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