Experimental drug

An experimental drug is a medicinal product (a drug or vaccine) that has not yet received approval from governmental regulatory authorities for routine use in human or veterinary medicine. A medicinal product may be approved for use in one disease or condition but still be considered experimental for other diseases or conditions.

United States

In the United States, the body responsible for approval is the Food and Drug Administration (FDA), which must grant the substance Investigational New Drug (IND) status before it can be tested in human clinical trials. IND status requires the drug's sponsor to submit an IND application that includes data from laboratory and animal testing for safety and efficacy.[1] A drug that is made from a living organism or its products undergoes the same approval process but is called a biologics license application (BLA). Biological drugs include antibodies, interleukins, and vaccines. In 2018 federal "Right to Try" laws were enacted in the United States, which allows individuals who fit into the criteria to try experimental drugs that are not yet deemed safe.[2]

Emergency Use Authorization (EUA)

The FDA has the authority to issue EUAs for medical products, including drugs and vaccines, during public health emergencies. This mechanism was prominently utilized during the COVID-19 pandemic, allowing for the rapid deployment of vaccines and therapeutics to address the crisis. The process for EUA includes the determination of a public health emergency, review of available scientific evidence, and consideration of the potential benefits and risks of the product.[3]

Canada

In Canada, a Clinical Trial Application (CTA) must be filed with the Health Products and Food Branch (HPFB) of Health Canada before starting a clinical trial. If the clinical trial results show that therapeutic effect of the drug outweighs negative side effects then the sponsor can then to file a New Drug Submission.[4]

European Union

Clinical trials in the European Union (EU) are regulated by the European Medicines Agency (EMA). Beginning in 2019 all applications for clinical trials must use a centralized EU portal and database. All clinical trial results will available to the public with the summary written in layperson's language.[5]

See also

References

  1. ^ "How Drugs are Developed and Approved". U.S. Food and Drug Administration. Retrieved July 27, 2018.
  2. ^ Mahant, Vijay (2020-06-23). ""Right-to-Try" experimental drugs: an overview". Journal of Translational Medicine. 18 (1): NA. doi:10.1186/s12967-020-02427-4. PMC 7309195. PMID 32576276.
  3. ^ Commissioner, Office of the (2024-03-04). "Emergency Use Authorization". FDA.
  4. ^ "How Drugs are Reviewed in Canada". Government of Canada. 8 January 2001. Retrieved July 27, 2018.
  5. ^ "European Medicines Agency – Clinical Trials Regulation". European Medicines Agency. Archived from the original on July 30, 2018. Retrieved July 30, 2018.

Public Domain This article incorporates public domain material from Dictionary of Cancer Terms. U.S. National Cancer Institute.

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