Divya S. Rajan, MD Internal Medicine - Nephrology Medicare: Accepting Medicare Assignments Practice Location: 1832 Harper Rd, Beckley, WV 25801 Phone: 681-207-7129 Fax: 681-207-7132 |
Dr. Hafiz Imran Iqbal, MD Internal Medicine - Nephrology Medicare: Accepting Medicare Assignments Practice Location: 242 George St, Beckley, WV 25801 Phone: 304-255-7878 Fax: 304-256-0060 |
Jose Jorge Gordinho, M.D. Internal Medicine - Nephrology Medicare: Not Enrolled in Medicare Practice Location: 2962 Robert C. Byrd Drive, Beckley, WV 25801 Phone: 304-254-9022 Fax: 304-254-9024 |
News Archive
Adamas Pharmaceuticals, Inc., a privately held company, announced today that it has entered into a Cooperative Research and Development Agreement (CRADA) with the United States Naval Health Research Center for preclinical studies evaluating Adamas' triple combination antiviral drug (TCAD) therapy for influenza A, including novel influenza A/H1N1. TCAD therapy includes Adamas' investigational proprietary fixed-dose oral combination drug, to be administered adjunctively with a neuraminidase inhibitor, including Tamiflu (oseltamivir phosphate, Roche).
A novel investigation into the impacts of neuronal mutations on autism-related characteristics in humans has been described in the open-access journal eLife.
ReShape Medical™, Inc. announced today that it has initiated a U.S. Investigational Device Exemption (IDE) clinical study to assess the safety and effectiveness of its non-surgical, dual-balloon device for weight loss. The ReShape Balloons are designed to be a treatment for the millions who want support with weight loss, without the invasiveness of surgery.
VeriChip Corporation ("VeriChip") and its development partner RECEPTORS LLC, a technology company whose AFFINITY by DESIGN™ chemistry platform can be applied to the development of selective binding products, announced today that VeriChip plans to fund its existing partnership with RECEPTORS to continue the development of a triage detection system for detection of the H1N1 virus.
CombinatoRx, Incorporated today announced that the U.S. Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) goal date for review of the Exalgo™ (hydromorphone HCl) extended-release tablets New Drug Application (NDA) from Monday, February 22, 2010 to Monday, March 1, 2010 due to federal government closings.
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