Top news of the week: 21.09.2022.
Media Update: Positive Dupixent® (dupilumab) Phase 3 data in children aged 6 months to 5 years with moderate-to-severe atopic dermatitis published...
Disease measures included additional EASI outcomes, itch reduction, percent of body surface area affected, skin pain, disease severity as measured by the Patient Oriented Eczema …
Biden Declares 'COVID-19 Pandemic Over' as Biopharma Reacts (Updated)
Pres. Joe Biden declared the COVID-19 pandemic over. Biopharma stocks react as vaccines and antivirals are still in development.
Takeda farms out cancer drug alisertib to Puma Biotech
Puma Biotech resurrects Takeda's aurora kinase A inhibitor alisertib, which failed a phase 3 trial in lymphoma, licensing rights to the drug in a deal worth up to $294m
Pfizer Builds On AI/ML Pact With CytoReason With New Five-Year Deal
<p><span>Deal Snapshot: The companies first partnered in January 2019, with a focus on more than 20 diseases. The renewed deal will support development of additional disease models using ...
Transformation Time For Minoryx With Leriglitazone Filing
<p>The Spanish biotech, formed in 2011, is preparing for the potential European launch of leriglitazone for X-linked adrenoleukodystrophy after the EMA accepted its file.</p> <br ...
Positive Dupixent® (dupilumab) Phase 3 Data in Children Aged 6 Months to 5 Years with Moderate-to-severe Atopic Dermatitis Published in The Lancet
Dupixent is the first and only biologic that significantly improved skin clearance, and reduced itch and overall disease severity in children as young as 6 months old in a Phase 3 trial ...
Bluebird lands another rare disease gene therapy OK — but there are a few caveats to note
Relative to the protracted journey of developing a gene therapy delivered by a lentiviral vector, the speed at which bluebird bio moved from having one approved product to two was extremely ...
Improving Clinical Attrition and Decision-Making with Artificial Intelligence
Register to learn how AI can augment and empower humans to make better quality decisions in R&D, leading to improved clinical attrition.