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The study will engage the laboratory of Dr. Charles Brenner, Roy J. Carver Chair of Biochemistry and Professor of Internal Medicine at University of Iowa. Brenner, is credited

FDA also said that the NDA would be treated as a Class 2 resubmission; hence, the new user fee goal date is 30 December 2014. In April 2014,

The trial is designed to confirm the positive results previously reported for ZS003, a phase III trial in which once-daily doses of ZS-9 maintained potassium levels within the

The sNDA for Olysio and sofosbuvir was submitted in May by the company’s strategic partner Janssen Research & Development. The regulatory submission is based on data from the

Harlan provides general and specialty toxicology services through its Contract Research Services (CRS) business. Under the deal, Harlan CRS will use Fluofarma’s expertise in high content analysis, biomarkers

The Brazilian pharmaceutical firm EMS will be responsible for securing regulatory and pricing approval, as well as the marketing and supply of the medication, in that territory. In

The drug is approved for use in combination with other agents, and will enable some patients to receive an all-oral therapy (without interferon injections), which represents a novel

Celsion’s reagent products are based on its newly acquired proprietary delivery platform technologies, TheraPlas and TheraSilence. TheraPlas and TheraSilence are designed for optimal transfection (intra-cellular delivery) of plasmid

The new line contains 44 vitamins and supplements with various benefits, including popular options such as probiotics, B-12, and multivitamins for both men and women. The radiance PLATINUM