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The company intends to start the trial upon investigational review board approvals and expects the first subject to be dosed within two months. LPA is a bioactive lipid

The company noted that validation of the applications confirms that the submissions are complete and starts the EMA’s centralized review process. In lung cancer, the proposed new indication

The expanded indication of Kyprolis is for these patients who have received at least one prior therapy. Currently, Kyprolis has accelerated approval in the US to treat patients

The drug is approved for patients with HAP and VAP known or suspected to be caused by susceptible isolates of Staphylococcus aureus including methicillin-susceptible and methicillin-resistant S. aureus

The study, approved by the Food and Drug Administration (FDA), was conducted at Northwestern Memorial Hospital. The therapeutic approach utilizing a patient’s own cells expanded in the laboratory

The formulation will be based on the Company’s proprietary ARCUS technology, and will be produced in collaboration with the Massachusetts Institute of Technology (MIT). RDS is a condition

The sNDS includes data to support: 1) High Dose Bolus administration of Aggrastat; and 2) an indication expansion for the reduction of major cardiovascular events in patients with

The patent claims are directed to the composition of matter and methods of use, including inhibiting tissue damage caused by ultraviolet radiation and promoting neurite outgrowth and neuron

The results were presented at the World Health Organization’s (WHO) fifth teleconference on Ebola vaccine clinical trials. The results showed that the Ebola GP Vaccine was highly immunogenic,