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The corollary to that message is that it's going to be awhile before the biotech is able to launch its obesity drug, Contrave. The Food and Drug Administration made the company run a clinical trial to confirm that there weren't any heart-related
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Jordo is a member of The Motley Fool Blog Network -- entries represent the personal opinions of our bloggers and are not formally edited. ccording to a report from the Drug Enforcement Administration (DEA), Belviq should be classified as a Schedule
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Contrave, which isn't even approved yet since it's waiting for safety trial data...The availability was noted on Qsymia's website and in an SEC disclosure...That'll get the job done, but don't expect the same kind of well-oiled machine that a launch
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Meena is a member of The Motley Fool Blog Network -- entries represent the personal opinions of our bloggers and are not formally edited. There is high risk in trying to time the biopharmaceutical market. Companies can lose in excess of half their
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FDA panel of experts that will make a recommendation on Lorcaserin, Arena's obesity medication. Studying the various social networking, discussion boards, blogs, and news, one can quickly sense two groups of participants: Those who are strongly
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FDA approval allows pharmaceutical and biotech companies to manufacture and sell drug treatments in the United States. Without approval, companies cannot sell or distribute treatments legally. Depending on the complexity of a drug, the number of
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Calif. (AP) — Drug developer Vivus Inc. says that regulators will take another three months to review the safety strategy on its proposed obesity drug Qnexa. The company says the Food and Drug Administration is now expected to
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Reuters U.S. drug regulators may have a hard time stopping millions of overweight Americans from taking a new obesity drug that many are likely to view as a miracle pill for slimming waistlines, despite its safety risks. Regulators and doctors are
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Ever offer to pay 6% more for your ticket because the plane was on time?...Arena has been guiding for a resubmission "around the end of the year."...Presumably the company waited until yesterday to announce the submission to make sure more investors
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Food and Drug Administration adding to its to-do list of required actions before the company could resubmit its marketing application for obesity drug lorcaserin. But the development-stage biotech pressed on and looks like it'll end the year ahead of
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