Dr. Galson Quotes

The doctors who perform approximately 2,200 heart transplants in the U.S. each year will now have a new option for enhancing successful outcomes.

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This new product will offer a much needed treatment option for patients suffering from this rare illness that, in some cases, has been found to progress to fatal forms of leukemia.

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There are dangers to consumers who purchase diet pills that contain drugs of unknown origin and quality.

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This approval is a welcome addition to the available defenses against the flu.

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It is our hope that the availability of inhaled insulin will offer patients more options to better control their blood sugars.

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Until today, patients with diabetes who need insulin to manage their disease had only one way to treat their condition. It is our hope that the availability of inhaled insulin will offer patients more options to better control their blood sugars.

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This has the potential to improve the quality of life for millions of Americans with diabetes.

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Today's approval is a major step forward in making breakthrough treatments available for patients with rare and difficult-to-treat forms of cancer.

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This approval is another example of the benefits of our agency's 'orphan' drugs program, which seeks to answer the medical needs of small groups of patients. The doctors who perform approximately 2,200 heart transplants in the U.S. each year will now have a new option for enhancing successful outcomes by preventing the rejection of the grafted organs.

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FDA is conducting a thorough evaluation of the safety profile for this drug in light of the recent publications. We're working to evaluate the potential risks and determine whether there is a need for further action. In the meantime, we advise providers to carefully assess the benefits and risks of the drug for their patients.

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We're working to evaluate the potential risks and determine whether there is a need for further action. In the meantime, we advise providers to carefully assess the benefits and risks of the drug for their patients.

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This approval is another example of the benefits of the Orphan Drug program, which provides incentives for the development of treatments for diseases affecting fewer than 200,000 patients in the United States a year. Until now, Pompe disease has had no approved treatment.

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Before beginning any human trials, the sponsor must perform extensive animal toxicity studies. Animal studies provide guidance on initial dosing and point to areas of safety needing special attention during human studies.

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This approval is another example of the benefits of the Orphan Drug program. Until now, Pompe disease has had no approved treatment.

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Phase 2 studies are typically well controlled and closely monitored and may involve up to several hundred patients. At the conclusion of these studies, FDA (Food and Drug Administration) and the sponsor usually meet to determine how the drug's development should be studied in Phase 3 and how to design and conduct further trials.

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