Teva’s Copaxone Reduces Disease Severity
Teva Pharmaceutical (Teva) has provided data that demonstrated patients treated for 10 and 15 years with Copaxone had significant reduction in disease severity. The long-term analysis utilised the
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.
Merck has updated the status of the clinical development programs for telcagepant (MK-0974) and MK-3207, the company’s investigational oral calcitonin gene-related peptide (CGRP) receptor antagonists for the intermittent