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Institute For OneWorld Health And Novartis Launch Innovative Collaboration To Discover And Develop Novel Therapy To Combat Diarrheal Disease
The Institute for OneWorld Health, the US-based non-profit pharmaceutical company that develops drugs for people with neglected infectious diseases in the developing world, today announced that it has launched a collaboration with global pharmaceutical leader Novartis to discover and develop a novel therapy for secretory diarrhea, a deadly disease that kills more than 1.6 million children in the developing world each year.
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HIV Infection And Chronic Drinking Have A Synergistic, Damaging Effect On The Brain
More than half of clinic patients infected with the human immunodeficiency virus (HIV) report they also drink heavily. While highly active antiretroviral therapy has helped to reduce HIV-related cognitive and motor deficits, neuropsychological deficits may continue and even be exacerbated by alcohol. A study of memory deficits has found that HIV infection and chronic alcoholism have synergistic, damaging effects on brain function.
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HIV Antibody Tests Unreliable For Early Infections In Teens
A previously healthy teenager shows up at the doctor"s office with a sore throat, fever, aches and general malaise. Routine blood tests are normal, an HIV test comes back negative, and the pediatrician sends the patient home with a diagnosis of acute viral infection.
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LEAD-6 Study Shows Better Results With Liraglutide Than Exenatide In Controlling Blood Glucose In Type 2 Diabetes

The results of the LEAD-6 study are published in an article Online First and in a future edition of The Lancet. The findings are presented at the same time at the American Diabetes Association meeting in New Orleans, USA. They indicate that taking liraglutide once a day is more efficient in controlling blood glucose in type 2 diabetes than the presently marketed treatment - two doses a day of exenatide. The way those two drugs (liraglutide and exenatide) function is by imitating the gut hormones (incretins) that are produced after eating food and that increase insulin production. Professor John Buse, of the University of North Carolina School of Medicine, Chapel Hill, NC, USA and collaborators studied 464 patients in a randomised trial. All of them were adults with uncontrolled type 2 diabetes receiving maximum tolerated doses of the diabetes drugs metformin, sulphonylurea, or both. The first group of 233 patients received liraglutide 1.8 mg once daily. The second group of 231 patients received exenatide 10 ÷µg twice-daily. The principal result was the change in glycosylated haemoglobin (HbA1c). HbA1c is used to indicate the average plasma glucose concentration of the preceding two to three months. In general, the reference range that is found in healthy persons who do not have diabetes is about 4 to 5.9 percent. Patients with diabetes usually have HbA1c levels above 6.5 percent. The average baseline HbA1c for the study population was 8.2 percent. With liraglutide the mean HbA1c was reduced by 1.12 percent. For patients on exenatide, the reduction was of 0.79 percent. The number of patients reaching an HbA1c level of less than 7.0 percent was higher in the liraglutide group (54 percent) than in the exenatide group (43 percent). In the liraglutide group, the mean fasting blood glucose levels were reduced by about two-and-a-half times more than in the exenatide group. On the other hand, exenatide was more effective in reducing blood glucose after breakfast and dinner meals, than liraglutide. These findings suggest that liraglutide makes greater use of its effects in the pre-meal or fasting phase. The use of each drug resulted in comparable weight loss, with 3.2kg with liraglutide and 2.9kg with exenatide. In general, both drugs were well accepted. But, with liraglutide there was less nausea and hypoglycaemia caused by low blood sugar was less frequent, than with exenatide. The authors write in conclusion: "Liraglutide once-daily provided significantly greater improvements in glycaemic control than did exenatide twice a day, and was generally better tolerated. The results suggest that liraglutide might be a treatment option for type 2 diabetes, especially when weight loss and risk of hypoglycaemia are major considerations." In a supplementary note, Dr Christophe De Block and Dr Luc Van Gaal, of the Antwerp University Hospital and the University of Antwerp, Belgium,remark: "The LEAD-6 trial shows that liraglutide provides greater improvements in glycaemic control and is better tolerated than exenatide; therefore, this [treatment] might be a good option for the treatment of type 2 diabetes." "Liraglutide once a day versus exenatide twice a day for type 2 diabetes: a 26-week randomised, parallel-group, multinational, open-label trial (LEAD-6)" John B Buse, Julio Rosenstock, Giorgio Sesti, Wolfgang E Schmidt, Eduard Montanya, Jason H Brett, Marcin Zychma, Lawrence Blonde, for the LEAD-6 Study Group DOI:10.1016/S0140-6736(09)60659-0 thelancet Written by Stephanie Brunner (B.A.) Copyright: Medical News Today Not to be reproduced without permission of Medical News Today


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