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An approval from EMA would make the drug available for the treatment of hyperkalaemia in all the 28 member states of the European Union along with Iceland, Liechtenstein

V212 is the firm’s investigational inactivated VZV vaccine to prevent herpes zoster (HZ) and HZ-related complications in immunocompromised subjects with the age of 18 years and above. The

Sapacitabine (CYC682), an orally-available nucleoside analogue, acts via a novel DNA single-strand breaking mechanism, resulting in production of DNA double strand breaks (DSBs) and/or checkpoint activation. Primary endpoint of

In addition to demonstrating that PBI-4050 is safe and very well tolerated, an objective of this study was to seek early evidence of a clinical benefit with PBI-4050

Through this collaboration, Incyte and Abramson have agreed to bring together the knowledge and expertise of their leading drug discovery and development scientists to conduct collaborative research aimed

The study showed that patients with well-controlled asthma have been able to change to the once-daily Relvar Ellipta (fluticasone furoate/vilanterol, FF/VI) 100/25, an inhaled corticosteroid (ICS)/long-acting beta2 agonist (LABA)

The trial met its objectives and identified a Phase 2 dose regimen. Celiac disease is an immune-mediated gastrointestinal disease caused by dietary gluten predominantly in individuals who carry

This financing was led by Topspin Biotech Fund and a group of investors with Euclidean Capital, with participation from existing investors InterWest Partners, OrbiMed Advisors, and Osage University

The phase 3 ADAPT clinical trial, which is assessing rocapuldencel-T in combination with sunitinib/standard-of-care for the treatment of metastatic renal cell carcinoma (mRCC), has been concluded as futility