Featured Stories
European Commission Approves First CRISPR Gene-Edited Therapy for Blood Disorder
The European Commission has approved CASGEVY™ (exagamglogene autotemcel) - the first CRISPR/Cas9 gene-edited therapy, for treating severe sickle cell disease (SCD) and transfusion-dependent beta thalassemia (TDT) in patients aged 12 and older.
Non-Opioid Drugs Show Promise in a New Generation of Pain Management Therapies
Latigo Biotherapeutics have just announced $135 million in Series A financing to develop non-opioid medicines for patients suffering from acute and chronic pain.
Tirzepatide Lowers Blood Pressure of Obesity Patients
Tirzepatide, Eli Lilly’s weight-loss drug most referred to by its brand names Mounjaro and Zepbound, has shown beneficial effects in relation to weight loss and glucose control. A
Amgen’s MariTide Demonstrates Weight Loss Potential
Further demonstrating the demand for weight loss drugs, recently published data for Amgen’s experimental obesity drug - MariTide - has shown significant weight loss within acceptable safety profiles in animal and early-stage human trials.
Vegan & Ketogenic Diets Found to Alter the Immune System
Starting a vegan or ketogenic diet can rapidly alter the immune system, a study reveals. Researchers found that switching to these diets triggers changes in the gut microbiome and immune cell populations within just four weeks.
Nanoform Announces Promising Clinical Results for Nanoenzalutamide
Nanoform Finland Plc., the medicine performance-enhancing company, announced that one of its leading nanoformulation drug products had received promising relative bioavailability results from its clinical study of nanocrystalline-enabled enzalutamide (nanoenzalutamide) tablet formulation.
Nanoform Commenced Relative Bioavailability Study of Nanotechnology- Enhanced Enzalutamide
Medicine performance-enhancing specialists Nanoform announced it had completed a relative bioavailability study of its nanocrystalline enabled enzalutamide as an alternative to an amorphous solid dispersion formulation of Xtandi®, the leading prescribed androgen receptor inhibitor approved to treat prostate cancer.
Colorcon Discuss Expedited Product Development and TiO2-Free Coatings
To expedite product development and accelerate time-to-market, Colorcon announced its HyperStart C2C™ Smart Formulation Hub, which helps formulators minimize the need for repetitive formulation iterations.