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The variant, a twelve-letter deletion in the ASGR1 gene on chromosome 17, was discovered by analyzing the entire genome and clinical information from across the population of Iceland.

The proceeds from the financing will be used to advance Mitochon’s lead compound MP101, a first in class mitochondrial targeted neuro-protective agent, into human studies, as well as,

The application was submitted to the FDA by Novartis in March 2016 under the ofatumumab collaboration between Novartis and Genmab. Priority Review is an FDA designation for drugs

Uptravi is indicated for the long-term treatment of pulmonary arterial hypertension (PAH) in adult patients with WHO functional class (FC) II-III, either as combination therapy in patients insufficiently

The reduction in workforce, which affects employees from Catalyst’s commercial team, is part of Catalyst’s ongoing efforts to conserve cash as it works to complete the requirements for

The partnership intends to discover, develop and commercialize novel therapies based on Agios’ cellular metabolism research platform. Celgene will pay Agios $200m upfront for an initial four-year research

The approval is based on overall response rate in cHL patients who have relapsed or progressed after autologous hematopoietic stem cell transplantation (auto-HSCT) and post-transplantation brentuximab vedotin. Opdivo

Benralizumab demonstrated significant reductions in the annual asthma exacerbation rate compared to placebo. The trials, Sirocco and Calima, assessed the safety and efficacy of two dose regimens of

Adzenys XR-ODT was approved by the U.S. Food and Drug Administration (FDA) in January for the treatment of ADHD in patients six years and older and is the