RSS FeedsMedPage Today Hematology/Oncology http://www.medpagetoday.com/rss/HematologyOncology.xml
Physicians.....get the latest breaking news on Hematology/Oncology. Free CME, accredited by the University of Pennsylvannia, is available for physicians and other medical professionals. Total news: 15 Last news: August 30, 2007 20:48:00
|
| FDA Approves Human Thrombin For Topical Use In Surgery August 31, 2007 08:00:00The U.S. Food and Drug Administration approved Evithrom (human thrombin), a blood-clotting protein used to help control bleeding during surgery.Evithrom is the first human thrombin approved since 1954 and is the only product currently licensed. It is derived from human plasma obtained from carefully screened and tested U.S. donors and has undergone steps to further reduce the risk for transfusion-transmitted diseases. [click link for full article] - [Read more] |
| Pharmions Oral Azacitidine Granted Fast Track Status For Myelodysplastic Syndromes August 30, 2007 07:00:00Pharmion Corporation (Nasdaq: PHRM) announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for oral Azacitidine in the treatment of Myelodysplastic Syndromes (MDS). Fast Track programs are designed to facilitate the development and expedite the review of new drugs that are intended to treat serious or life-threatening conditions and that demonstrate the potential to address unmet medical needs. [click link for full article] - [Read more] |
| FDA Approves New Roche West Nile Virus Blood Screening Test August 29, 2007 07:00:00Roche Diagnostics announced that the US Food & Drug Administration (FDA) today approved its biologics license application for the companys test for direct detection of West Nile Virus in donated human blood and plasma. West Nile virus, which can cause serious health issues, is transmitted to humans most often through mosquito bites, but can also less commonly be transmitted by transfusion of infected blood or blood products. [click link for full article] - [Read more] |
| Human Thrombin Gets FDA Approval August 28, 2007 21:10:08ROCKVILLE, Md. -- The FDA today allowed a human thrombin (Evithrom) on the market after the risk of transfusion-transmitted viral infection kept it on the sidelines for more than a half-century. - [Read more] |
| H. pylori Cancer Risk Tracked to Specific Genotype August 28, 2007 20:01:02LYON, France -- The severity of precancerous lesions tracks to specific bacterial strains, investigators here reported, strengthening the association between Helicobacter pylori infection and gastric cancer. - [Read more] |
| News From The Journal Of Clinical Investigation August 28, 2007 18:00:00System overload: infusion of IgG helps clear therapeutic and imaging antibodies from the circulationThe use of monoclonal IgG antibodies attached to toxins or radioactive substances for treating and imaging cancer is currently limited by the ability of IgG to remain in the blood for a long time because this decreases the tumor-to-background contrast and increases normal tissue toxicity. [click link for full article] - [Read more] |
| Protalix BioTherapeutics Treats First Patient In Phase III Clinical Trial Of PrGCD August 28, 2007 07:00:00Protalix BioTherapeutics, Inc. (Amex: PLX), announced that it has treated the first patient in its phase III clinical trial of the Companys lead product candidate, prGCD, a proprietary plant cell expressed recombinant form of human Glucocerebrosidase (GCD) for the treatment of Gaucher disease, a lysosomal storage disorder in humans. The phase III clinical trial will take place in centers in the United States, Israel and other locations worldwide. [click link for full article] - [Read more] |
| Cervical Cancer Screening Goes Do-It-Yourself August 27, 2007 20:04:00VANCOUVER, British Columbia -- Asking patients to collect their own vaginal specimens for HPV testing proved an effective initial screening method among high-risk women, researchers here found. - [Read more] |
| Response By American College Of Medical Genetics To New FDA Labeling Decision For Warfarin August 27, 2007 20:00:00On August 16, the Food and Drug Administration approved new labeling information for the blood-thinner warfarin, sold under the brand name Coumadin. The new label suggests that one can prescribe higher or lower doses that may be safer for patients with variations in two genes, CYP2C9 or VKORC1. These variations can be learned through genetic testing, which may be a useful tool in determining appropriate dosing levels for individual patients and lower risks of bleeding complications. [click link for full article] - [Read more] |
| Wyeth Receives Approval From European Medicines Agency For New BeneFIX Features August 26, 2007 07:00:00Wyeth Pharmaceuticals, a division of Wyeth (NYSE:WYE), announced that it has received approval from the European Medicines Agency (EMEA) for new enhancements for BeneFIX® nonacog alfa (Recombinant Coagulation Factor IX). These enhancements are designed to offer patients a simpler and more convenient preparation process compared with the original BeneFIX preparation process. [click link for full article] - [Read more] |
|
|