Articles By Cyndi Root
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Teva, Active Biotech Expand Laquinimod Program In Neurodegenerative Diseases
11/7/2014
Teva Pharmaceutical Industries and Active Biotech have expanded their partnership with new trials of laquinimod.
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Amgen's 1st Phase 3 Trial For Trebananib Reveals Disappointing Results
11/7/2014
Amgen announced secondary endpoint results from the TRINOVA-1 trial of trebananib in women with recurrent ovarian cancer.
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Oncology Trials Facing Longer Cycle Times, Report Finds
11/6/2014
According to a new KMR Group report, oncology trials are now taking longer to complete. KMR announced its findings in a press release, stating that late-stage oncology cycle times have increased in the last 10 years.
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ex scientia, Sunovion Partner On Treatments For Psychiatric Disorders
11/6/2014
ex scientia has partnered with Sunovion Pharmaceuticals on treatments for psychiatric disorders.
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Kamada's Glassia Granted FDA Orphan Drug Status For Graft Versus Host Disease
10/31/2014
Kamada announced in a press release that the Food and Drug Administration (FDA) has granted Glassia Orphan Drug status for the treatment of Graft-versus-host-disease (GVHD).
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FDA Delays Decision On NPS' Natpara BLA For Hypoparathyroidism
10/29/2014
NPS Pharmaceuticals made a major amendment to its Biologics License Application (BLA) for Natpara, causing the Food and Drug Administration (FDA) to delay its decision for another three months.
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FDA Approves Arbor's Sotylize For Arrhythmias, Atrial Fibrillation
10/29/2014
Arbor Pharmaceuticals has provided a new sotalol hydrochloride oral solution, Sotylize, for treatment of ventricular arrhythmias and maintenance of normal sinus rhythm in patients with atrial fibrillation/flutter
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FDA Allows Cytori To Resume ADRC Trial In Ischemic Heart Disease
10/29/2014
Cytori Therapeutics has been allowed to resume its ATHENA trials for adipose-derived regenerative cells (ADRCs) in heart failure patients with ischemic heart disease.
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BCRP Blood Cancer Consortium Expands Clinical Trial Base
10/29/2014
The Blood Cancer Research Partnership (BCRP) and the Dana-Farber Cancer Institute, the lead institute of the BCRP, have announced an expansion of the collaborative effort that includes Harvard University and members of industry.
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Relypsa Submits NDA For Patiromer In Hyperkalemia
10/28/2014
Relypsa has submitted a New Drug Application (NDA) to the Food and Drug Administration (FDA) for patiromer in the treatment of hyperkalemia.