
News
U.S. FDA approves generic versions of Novartis blockbuster MS treatment
Dec 6, 2019
(Reuters) - The U.S. Food and Drug Administration on Thursday approved three generic versions of Swiss drugmaker Novartis AG's top-selling multiple sclerosis (MS) medicine Gilenya.The capital injection turns Blackstone into a long-term strategic investor and promotes the next phase of HEC Pharm’s growth strategy to cement its market position in China
Polaris Group ADI-PEG20 on the cover of AACR journals
Dec 10, 2019
Pancreatic cancer is notoriously difficult to treat. One potential opportunity for targeting pancreatic cancer is through its modified amino acid metabolism. Specifically, depriving arginine-dependent tumor cells of arginine can lead to cell death. To achieve this, a polyethylene glycol (PEG)-conjugated arginine deiminase construct (ADI-PEG20) was previously designed and tested as a monotherapy in clinical studies with limited success.
First Five Subjects Randomized in SyneuRx’ SND12 PhaseIIb/III Study of Clozaben®, a Novel Traetment for Refractory Schizophrenia
May 22, 2017
SyneuRx International (Taiwan) Corp. today announced that the first five subjects have been randomized for the company’s SND12 Phase IIb/III clinical trial. The trial will study the efficacy and safety of one of its leading investigational therapies, Clozaben®, for adult subjects with schizophrenia who are refractory to current treatments available.
First Three Subjects Randomized in SyneuRx’s SND13 Phase IIb/III NaBen© Schizophrenia Trial
May 11, 2017
SyneuRx International (Taiwan) Corp. today announced that the first three subjects have been randomized from the 11 subjects screened into the company’s SND13 Phase IIb/III clinical trial within a short period of time. The trial will study the efficacy and safety of its leading investigational therapy NaBen© for adult subjects between 18 and 55 years of age with schizophrenia.




