This article is missing information about "conditional/accelerated approval" in its many flavors; doi:10.3389/fmed.2021.818647 may help. (December 2022) |
An approved drug is a medicinal preparation that has been validated for a therapeutic use by a ruling authority of a government.[1] This process is usually specific by country, unless specified otherwise.
Process by country
editUnited States
editIn the United States, the FDA approves drugs. Before a drug can be prescribed, it must undergo the FDA's approval process. While a drug can feasibly be used off-label (for non-approved indications), it still is required to be approved for a specific disease or medical condition.[2] Drug companies seeking to sell a drug in the United States must first test it. The company then sends the Food and Drug Administration's Center for Drug Evaluation and Research (CDER)[3] evidence from these tests to prove the drug is safe and effective for its intended use. A fee is required to make such FDA submission. For financial year 2020, this fee was: for an application requiring clinical data ($2,942,965) and for an application not requiring clinical data ($1,471,483).[4] A team of CDER physicians, statisticians, chemists, pharmacologists, and other scientists reviews the company's data and proposed labeling. If this independent and unbiased review establishes that a drug's health benefits outweigh its known risks, the drug is approved for sale. The center doesn't actually test drugs itself, although it does conduct limited research in the areas of drug quality, safety, and effectiveness standards.
As of the end of 2013, the FDA and its predecessors had approved 1,452 drugs, though not all are still available, and some have been withdrawn for safety reasons.[5] Accounting for subsequent corporate acquisitions, these approvals were earned by approximately 100 different organizations.[5]
European Union
editIn the European Union, it is the European Medicines Agency (EMA) that evaluates medicinal products.
Japan
editIn Japan, the agency regulating medicinal products is Pharmaceuticals and Medical Devices Agency (PMDA).
Approval
editOn average, only one in every 5,000 compounds that makes it through lead development to the stage of preclinical development becomes an approved drug. Only 10% of all drugs started in human clinical trials become an approved drug.[6][7][8]
See also
editReferences
edit- ^ "Development and approval process (Drugs)". US Food and Drug Administration. 13 June 2018. Retrieved 4 May 2019.
- ^ Commissioner, Office of the (2019-04-18). "Understanding Unapproved Use of Approved Drugs "Off Label"". FDA. Retrieved 2021-04-21.
- ^ Research, Center for Drug Evaluation and. "About the Center for Drug Evaluation and Research". www.fda.gov. Retrieved 2018-01-21.
- ^ "Prescription Drug User Fee Rates for Fiscal Year 2020". USA (Federal register). Retrieved 9 August 2019.
- ^ a b How Many Drugs has FDA Approved in its Entire History? New Paper Explains
- ^ Ezekiel J. Emanuel (9 September 2015). "The Solution to Drug Prices". The New York Times.
On average, only one in every 5,000 compounds that drug companies discover and put through preclinical testing becomes an approved drug. Of the drugs started in clinical trials on humans, only 10 percent secure F.D.A. approval. ...
- ^ Wong, Chi Heem; Siah, Kien Wei; Lo, Andrew W (31 January 2018). "Estimation of clinical trial success rates and related parameters". Biostatistics. 20 (2): 273–286. doi:10.1093/biostatistics/kxx069. ISSN 1465-4644. PMC 6409418. PMID 29394327.
- ^ Lowe, Derek (2 February 2018). "A New Look at Clinical Success Rates". In the Pipeline, American Association for the Advancement of Science. Retrieved 4 May 2019.
