Pre-clinical development


Pre-clinical development

Pre-clinical development is a stage of research that begins before clinical trials (testing in humans) can begin, and during which important feasibility, iterative testing and safety (also known as Good Laboratory Practice or "GLP") data is collected.

The main goals of pre-clinical studies (also named preclinical studies and nonclinical studies) are to determine a product's ultimate safety profile. Products may include new or iterated or like-kind medical devices, drugs, gene therapy solutions, etc. Each class of product may undergo different types of preclinical research. For instance, drugs may undergo pharmacodynamics (PD), pharmacokinetics (PK), ADME, and toxicity testing through animal testing. This data allows researchers to allometrically estimate a safe starting dose of the drug for clinical trials in humans. Medical devices that do not have drug attached will not undergo these additional tests and may go directly to GLP testing for safety of the device and its components. Some medical devices will also undergo biocompatibility testing which helps to show whether a component of the device or all components are sustainable in a living model. Most pre-clinical studies must adhere to Good Laboratory Practices (GLP) in ICH Guidelines to be acceptable for submission to regulatory agencies such as the Food & Drug Administration in the United States.

Typically, both "in vitro" and "in vivo" tests will be performed. Studies of a drug's toxicity include which organs are targeted by that drug, as well as if there are any long-term carcinogenic effects or toxic effects on mammalian reproduction.

The information collected from these studies is vital so that safe human testing can begin. Typically, in drug development studies animal testing involves two species. The most commonly used models are murine and canine, although primate and porcine are also used. The choice of species is based on which will give the best correlation to human trials. Differences in the gut, enzyme activity, circulatory system, or other considerations make certain models more appropriate based on the dosage form, site of activity, or noxious metabolites. For example, canines may not be good models for solid oral dosage forms because the characteristic carnivore intestine is underdeveloped compared to the omnivore's, and gastric emptying rates are increased. Also, rodents can not act as models for antibiotic drugs because the resulting alteration to their intestinal flora causes significant adverse effects.1 Depending on a drugs functional groups, it may be metabolized in similar or different ways between species, which will effect both efficacy and toxicology. Medical device studies also use this basic premise. Most studies are performed in larger species such as dogs, pigs and sheep which allow for testing in a similar sized model as that of a human. In addition, some species are used for similarity in specific organs or organ system physiology (swine for dermatological and coronary stent studies; goats for mammary implant studies; dogs for gastric studies; etc).

Based on pre-clinical trials, No Observable Effect Levels (NOEL) on drugs are established, which are used to determine initial phase 1 clinical trial dosage levels on a mass API per mass patient basis. Generally a 1/100 uncertainty factor or "safety margin" is included to account for interspecies (1/10) and inter-individual (1/10) differences).2

Animal testing in the research-based pharmaceutical industry has been reduced in recent years both for ethical and cost reasons. However, most research will still involve animal based testing for the need of similarity in anatomy and physiology that is required for diverse product development.

ee also

*Drug Discovery Hit to Lead
*Drug development
*Nonclinical studies
*Pharmacodynamics
*Pharmacokinetics
*Absorption, Distribution, Metabolism, and Excretion
*Simcyp Simulator
*Caco-2
*Pharmaceutical company

Resources

#Martinez, M.N. Interspecies Differences in Physiology and Pharmacology: Extrapolating Preclinical Data to Human Populations. Rogge, M.C. Taft, D.R Preclinical Development Vol 152 2005. ISBN 1-57444-882-X
#Amdur, M.O. Doull, J.D. Klaassen, C.D. Toxicology: The Basic Science of Poisons. 1991.

External links

* [http://www.fda.gov/cder/handbook/preclin.htm FDA requirements Pre-Clinical Research]
* [http://www.biomedcode.com BioMedCode Pre-Clinical Research]
* [http://www.iris-pharma.com Iris Pharma Pre-Clinical Research in Ophthalmology]
* [http://www.visionar.se/?lang=en VISIONAR Preclinical (CRO)]


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