Publication

Drug development: longer-lived proteins

Jeffrey Alan Hubbell, Stephane Kontos
2012
Reviews

Résumé

Protein therapeutics represent a powerful class of clinically approved drugs for the prevention and treatment of various diseases. Once administered, the biological fate of protein therapeutics is governed by the body's various complex biochemical and biophysical clearance mechanisms, several of which may decrease the drug's circulation time and efficiency. In this tutorial review, we introduce the concepts of physiological protein clearance from the body, and describe several chemical modification and protein engineering approaches used to improve the life span of administered protein therapeutics.

Source officielle

https://infoscience.epfl.ch/entities/publication/992fb54e-8782-4b18-9bac-7c92c8820216

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Jeffrey Alan Hubbell, Stephane Kontos
2012
Reviews

Résumé

Source officielle

https://infoscience.epfl.ch/entities/publication/992fb54e-8782-4b18-9bac-7c92c8820216

À propos de ce résultat

Concepts associés (24)

Food and Drug Administration

La Food and Drug Administration (FDA, en français : « Agence fédérale américaine des produits alimentaires et médicamenteux ») est l'administration américaine des denrées alimentaires et des médicaments. Cet organisme a, entre autres, le mandat d'autoriser la commercialisation des médicaments sur le territoire des États-Unis.

Approved drug

An approved drug is a medicinal preparation that has been validated for a therapeutic use by a ruling authority of a government. This process is usually specific by country, unless specified otherwise. In 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.

Drug development

Drug development is the process of bringing a new pharmaceutical drug to the market once a lead compound has been identified through the process of drug discovery. It includes preclinical research on microorganisms and animals, filing for regulatory status, such as via the United States Food and Drug Administration for an investigational new drug to initiate clinical trials on humans, and may include the step of obtaining regulatory approval with a new drug application to market the drug.

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