European Commission approves Keryx’s Fexeric for elevated serum phosphorous
Keryx carried out a phase 2, non-dialysis study and a 58-week, phase 3 registration trial on about 1900 patients. The company said in the phase 3 trial, ferric
Axsome Therapeutics has received the US Food and Drug Administration (FDA) approval for Auvelity (dextromethorphan HBr and bupropion HCl) to treat agitation associated with dementia due to Alzheimer’s.
The company started enrolling patients in IFN-K-002 double-blind, randomized, placebo-controlled, multi-center study to identify the biological and clinical efficacy of IFNa-Kinoid in patients suffering from SLE. Neovacs intends
CVS/pharmacy has expanded the availability of the opioid overdose reversal medicine, naloxone, in several states. The medication was already available at CVS/pharmacy without a prescription in Rhode Island
The joint research and development effort would leverage Purdue Pharma’s intellectual property and lead compounds, combined with AnaBios’ Phase-X technology. Purdue Pharma has more than 10 years of
The state-of-the-art facility provides the translational bridge between pre-clinical development and phase II clinical trials with end-to-end capabilities, including process development, cell banking, cGMP manufacturing, purification and formulation,