Many researchers believed that the toxin Panton-Valentine leukocidin (PVL) was the cause of community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) as it could be found in all CA-MRSA strains. But
The trials are designed to test the safety and efficacy of pre-seasonal treatment with PreHistin on moderate to moderately severe seasonal ragweed allergy patients. The phase III trials
Data from the study indicate that the combination regimen was well tolerated with preliminary anti-tumor activity observed. These patients are at high risk for having disease which has
Under the terms of the agreement, Inovio will receive from Wyeth a $4.5 million upfront license fee, annual license maintenance fees, research support, and up to $60 million
PTC299 is an orally bioavailable drug designed to modulate RNA-mediated protein expression to inhibit the production of vascular endothelial growth factor (VEGF) in tumors. PTC has recently completed
All 26 EU member states have agreed to issue national approval to Prexige. Novartis also reported that the drug has been authorized in Canada. Initial approval for Prexige
The drug, a lipid-lowering agent which helps to prevent a stroke or heart attack, falls in the cardiovascular segment of the market, the company noted. Cadila said it
The phase I trial evaluated the safety and tolerability of VRX496, enrolling five subjects with HIV infection who had failed to respond to the standard treatment for HIV,
This phase III trial will specifically study patients with advanced non-small cell lung cancer (NSCLC). It will evaluate NOV-002 in combination with paclitaxel and carboplatin versus paclitaxel and
Antigen Express, a wholly owned subsidiary of Generex, designed the vaccine using its proprietary platform technology and has been conducting preclinical studies since 2004. Generex commented that the
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