Articles By Cyndi Root
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Merrimack Pharmaceuticals' MM-141 Named FDA Orphan Drug For Pancreatic Cancer
11/10/2014
Merrimack Pharmaceuticals announced in a press release that the Food and Drug Administration (FDA) granted Orphan Drug designation to MM-141.
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Astellas', Basilea's Isavuconazole Granted FDA Orphan Drug Status For Invasive Candidiasis
11/9/2014
Astellas’ and Basilea’s Isavuconazole continues its upwards trajectory as the Food and Drug Administration (FDA) has granted the agent Orphan Drug status for invasive candidiasis.
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Abide Therapeutics, University Of Oxford Collaborate On Serine Hydrolases
11/9/2014
Abide Therapeutics has partnered with the University of Oxford to research serine hydrolases, an under explored enzyme class.
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Proteostasis, Astellas Partner On Unfolded Protein Response Therapeutics
11/7/2014
Proteostasis Therapeutics and Astellas Pharma have begun a partnership to develop therapeutics modulating the Unfolded Protein Response (UPR).
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FDA Clears ISCO's Parthenogenetic Stem Cells For Investigational Clinical Use
11/7/2014
International Stem Cell Corporation is now approved to manufacture human parthenogenetic stem cells.
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SCYNEXIS Licenses SCY-635 To Waterstone For Viral Diseases
11/6/2014
SCYNEXIS has licensed SCY-635 to Waterstone Pharmaceutical for the treatment of human viral diseases. SCYNEXIS announced the move in a press release, stating that it allows the company to focus on other compounds in development.
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Bristol-Myers Squibb Acquires Galecto Biotech, Galectin-3 Inhibitor For IPF
11/5/2014
Bristol-Myers Squibb (BMS) has acquired an option to buy Galecto Biotech AB and the worldwide rights to TD139.
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New Life In Cancer Drugs Targretin, Tasigna For Alzheimer's, Study Finds
11/5/2014
New research has found that cancer drugs Targretin and Tasigna may be effective in treating Alzheimer’s Disease.
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FDA Committee Recommends Daiichi Sankyo's Savaysa For Stroke
11/4/2014
A Food and Drug Administration (FDA) committee voted 9 to 1 to recommend Daiichi Sankyo’s Savaysa (edoxaban) for the reduction in risk of stroke and systemic embolic events (SEE) in patients with non-valvular atrial fibrillation (NVAF).
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FDA Awards Orphan Status To RetroSense's RST-001 For Retinitis Pigmentosa
11/4/2014
RetroSense Therapeutics announced in a press release that the Food and Drug Administration (FDA) has granted Orphan Drug status to RST-001.