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This patent is entitled "Method of Synthesis of Substituted Hexitols Such as Dianydrogalactitol," and provides a patent term that lasts until 2030. "This allowance represents our second U.S.

A master drug file contains all of the information that regulatory agencies require as part of the drug development and approval process. Such information includes preclinical data, GMP

SPCD is an alternative method for conducting well-controlled clinical trials that substantially decreases the impact on trial outcomes of any placebo effect and will enable PPD’s clients to

The patent covers CPMA, a new polymer drug delivery platform technology developed by Rexahn. "We are pleased to further expand our platform of proprietary drug delivery technologies in

In the program, the company will investigate PEGPH20 (PEGylated recombinant human hyaluronidase) to show improvement in overall survival (OS). The FDA fast track status will help in the

The company said that duvelisib has shown clinical activity across a range of blood cancers, including indolent non-Hodgkin lymphoma (iNHL) and chronic lymphocytic leukemia (CLL). Currently, the safety

Apart from Sweden, ILUVIEN is currently approved for marketing in Austria, Denmark, France, Germany, Italy, Norway, Portugal, Spain and the UK, and is commercially available in the UK

In March 2000, the US Food and Drug Administration approved Zonegran as adjunctive therapy in the treatment of partial seizures in adults with epilepsy. Under the deal, Eisai

Under the deal, the two firms will work together to advance the next frontier of bi-specific antibody development platforms and bring new therapies to patients in need. CMC