Pre-clinical pipeline expanded with novel wholly-owned candidates PN-477, an oral and s.c. triple GLP-GIP-GCG agonist and PN-458, an oral and s.c. dual GLP-GIP agonist, and PN-8047, an oral hepcidin ...
NDA for rusfertide submitted to the US Food and Drug Administration (FDA), with potential approval and launch this ...
Celtic pull off their first win on German soil but are still knocked out of the Europa League knockout play-offs by Stuttgart ...
Objective To assess whether post-authorisation studies registered with the European Medicines Agency (EMA) adhere to legislation and recommendations to publicly post study protocols and results.
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