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The companies will establish a joint venture (JV) and each share equally in the initial investment. Subject to necessary regulatory approvals, the construction on the initial phase of the facility

If approved, Tafinlar + Mekinist will be the first targeted treatment available for patients with BRAF V600-positive NSCLC. Of the estimated 1.8 million new cases of lung cancer

A poster was presented by the clinical investigators in a poster session at the American Society of Clinical Oncology and Society for Imumunotherapy of Cancer (ASCO-SITC) Clinical Immuno-Oncology

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)