Once-daily oral treatment was well-tolerated and demonstrated a good safety profile in Phase IIb study
Once-daily oral treatment was well-tolerated and demonstrated a good safety profile in Phase IIb study
Phase II/III TeenCOVE study met primary endpoint of non-inferior immunogenicity versus adult comparator group
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The updated draft guidance comes following recent research comparing induction times
CHMP recommended EU approval for combination treatment in its May decisions
Vaccine candidate demonstrated 83.6% efficacy against hospitalisation three years after vaccination
European approval follows the recent announcement of the FDA approval of Ponvory for RMS
Collaboration will aim to address challenge of timely and costly AAV-based vector manufacturing
At six and a half years 49% of patients treated with combination therapy remained alive
First targeted treatment authorised in the US for NSCLC patients with EGFR exon 20 insertion mutations
First one-time gene therapy for CALD among latest recommendations
Investigational 15-valent pneumococcal conjugate vaccine consists of pneumococcal polysaccharides from 15 serotypes
Investigational therapy also led to superior body weight reductions in adults with type 2 diabetes
Pfizer/BioNTech said all doses earmarked for the European Commission are planned to be manufactured in the European Union