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WASHINGTON (Reuters) - A new regulatory pathway could shave years off the traditional drug approval process in the United States, according to some companies whose drugs have been given "breakthrough therapy" designation by the U.S. Food and Drug Ad
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NEW YORK (Reuters Health) - Exercise-based rehabilitation programs for heart patients are tied to health benefits even among the most elderly, according to a new study.img width='1' height='1' src='http://reuters.us.feedsportal.com/c/35217/f/654207/
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KANSAS CITY, Missouri (Reuters) - Sex researcher Virginia Johnson, part of the famed Masters and Johnson team who conducted groundbreaking work on human sexuality, has died in St. Louis at the age of 88, her son said on Thursday.img width='1' height
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NEW YORK (Reuters Health) - U.S. law requires certain research results to be posted online within a year of a study's end date, but a new analysis found that only about half of cancer drug research results are made public after three years.img width
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(Reuters) - Vertex Pharmaceuticals Inc said U.S. health regulators placed a partial clinical hold on its mid-stage study of an experimental oral hepatitis C treatment because of potential liver problems, sending its shares sharply lower on Thursday.
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(Reuters) - The U.S. Food and Drug Administration granted marketing approval to Cepheid's tuberculosis test that checks if the disease-causing bacteria carry antibiotic-resistant genetic markers.img width='1' height='1' src='http://reuters.us.feedsp
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LONDON (Reuters) - Despite its high current death rate, the Middle East Respiratory Syndrome (MERS) that emerged in Saudi Arabia last year is unlikely to cause a SARS-like epidemic because it is not spreading as easily, scientists said on Friday.img
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LONDON (Reuters) - European drugs regulators have found no new safety concerns with diabetes drugs known as GLP-1 and DPP-4 therapies after concluding a safety review of possible links to damage to the pancreas.img width='1' height='1' src='http://r
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