Results 301 to 310 of about 1,536,180 (350)
Some of the next articles are maybe not open access.
Nature Reviews Drug Discovery, 2018
This corrects the article DOI: 10.1038/nrd.2018.4.
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This corrects the article DOI: 10.1038/nrd.2018.4.
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Science, 2005
We are concerned about misinformation in the News Focus article “Lupus drug company asks FDA for second chance” (J. Couzin, 11 Feb., p. [835][1]). It is not true that the U.S. Food and Drug Administration (FDA) has rejected the medication LJP 394, which is under active development by La Jolla Pharmaceutical Company.
Joan T. Merrill, Sandra Raymond
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We are concerned about misinformation in the News Focus article “Lupus drug company asks FDA for second chance” (J. Couzin, 11 Feb., p. [835][1]). It is not true that the U.S. Food and Drug Administration (FDA) has rejected the medication LJP 394, which is under active development by La Jolla Pharmaceutical Company.
Joan T. Merrill, Sandra Raymond
openaire +3 more sources
Drug Information Journal, 1992
The Passport to Drug Approval in Europe will be changed in the future. The proposal of the Commission of the European Economic Community (EC) for the free movement of medicinal products in the future is discussed. After a short discussion of the proposal, information is given on the influence outside the EC, on what happens in the EC, and the influence
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The Passport to Drug Approval in Europe will be changed in the future. The proposal of the Commission of the European Economic Community (EC) for the free movement of medicinal products in the future is discussed. After a short discussion of the proposal, information is given on the influence outside the EC, on what happens in the EC, and the influence
openaire +2 more sources
Accelerating drug development and approval
Drug News & Perspectives, 2010Regulatory agencies are the gateway between the pharma/biotech industry and patients and can serve as stimulators of new drug development. This article highlights several means of doing so implemented thus far, many with already impressive histories, such as orphan drug legislation, and others of a more experimental nature, such as the FDA's priority ...
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Nature Reviews Drug Discovery, 2010
In a year in which regulators and drug companies gained familiarity with risk management strategies, the number of new drug approvals was similar to that in 2008.
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In a year in which regulators and drug companies gained familiarity with risk management strategies, the number of new drug approvals was similar to that in 2008.
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T-PA and the Principles of Drug Approval
New England Journal of Medicine, 1987The recent approval by the Food and Drug Administration of tissue plasminogen activator (t-PA) for clot lysis and preservation of myocardial function in patients with acute myocardial infarction ha...
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Non-Approved Use of Food and Drug Administration Approved Drugs
American Journal of Ophthalmology, 1979Joseph I. Goldstein, Joel S. Mindel
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The foundations of immune checkpoint blockade and the ipilimumab approval decennial
Nature Reviews Drug Discovery, 2022Nils Lonberg +2 more
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