SFDA Approves Abbott’s XIENCE V Drug Eluting Stent
The Chinese State Food and Drug Administration (SFDA) has approved Abbott’s XIENCE V Everolimus Eluting Coronary Stent System for the treatment of coronary artery disease (CAD) The company
The US Food and Drug Administration (FDA) has declined to approve Unicycive Therapeutics’ resubmitted new drug application (NDA) for oxylanthanum carbonate (OLC) to treat hyperphosphatemia in chronic kidney disease (CKD) patients on dialysis.
Addex Pharmaceuticals’ (Addex) ADX10059 has demonstrated significant potential in a non-human primate model of Parkinson’s disease levodopa induced dyskinesia (PD-LID). ADX10059 is an allosteric inhibitor – a negative
Tobira Therapeutics (Tobira) has reported pharmacokinetic data and results from a double-blind, placebo-controlled, multiple-dose randomised study of TBR-652 in sixty healthy volunteers. TBR-652, a CCR5 antagonist under investigation