European approval follows the recent announcement of the FDA approval of Ponvory for RMS
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
UK-based charity Breast Cancer Now ‘proud’ of milestone after campaigning for improved data collection
The 2021 Clinical Researcher of the Year – The Americas will be closing for entry on the 18th of June.
If approved, up to 2,000 children with CF would be eligible for treatment with the drug
Cost-effectiveness estimates have fallen above the threshold because of uncertain trial evidence
Around 270 people with PNH and 160 people with aHUS will be eligible for the new treatment
BMS will pay Agenus $200m upfront and up to $1.36bn in development, regulatory and commercial milestones
Initial results trialling seven vaccines will inform plans for Autumn booster programme