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Before a new drug, surgical procedure, or therapy becomes available to the

public, it must go through a rigorous testing process and be evaluated by the US

Food and Drug Administration (FDA). This testing process consists of a series of

clinical trials that are designed to test the safety and usefulness of the new

drug compared to the current standard treatment.

The clinical trials that make headlines are usually what are called phase III

trials. These are large-scale tests with hundreds or thousands of patients. They

are the culmination of earlier phase I and phase II trials that include many

fewer people and still earlier preclinical experiments with animals. They are

also the final tests in humans before the FDA is asked to authorize sale of new

medicines.

Why Are Large-Scale Trials

Needed?

Clinical trials are designed to test whether a drug is safe for humans, and

whether the drug is effective in treating human diseases or conditions. Although

the drug has generally gone through extensive animal testing before the trial

begins, animal trials cannot always predict how new medicines will affect

humans. Even the most painstaking tests with animals give only approximate

indications of how people will respond to drugs. At some point, after thorough

study in animals (and when the FDA is convinced human experimentation will

probably be safe), tests with humans become necessary.

Not only is it necessary to test new drugs in humans, but they need to be

tested in a large number of humans in order for the results of the trial to be

clear. The reason so many volunteers are required is that people are highly

variable in how they respond to drugs. It is not unusual, for example, for a

drug be somewhat effective in only 30 percent of those who take it. For medical

researchers to prove such a slight benefit requires testing the drug in as many

as several thousand patients.

This extensive testing is part of what drives up the cost of new drugs – the

average development time is over 10 years and costs from 500 to 700 million

dollars.

What Goes on Prior to a Large-Scale

Phase III Trial?

An enormous amount of testing has gone on by the time a drug is ready for

phase III. In general, a new drug or treatment goes through preclinical testing

in animals, then small phase I and phase II trials in humans before being ready

for large-scale testing.

Preclinical testing

When a drug is discovered that seems to have medical potential, a drug

company will test it exhaustively in animals, looking for signs it may be

poisonous, cause cancer, or cause birth defects. Animal studies will also be

used to estimate the initial drug doses to be tested in humans.

When animal experiments are finished, the company asks the FDA for permission

to begin clinical trials. The FDA only grants approval once they are satisfied

that the animal experiments are sound and that clinical trials are likely to be

safe.

Phase I

The Types of Clinical Trials  was originally published on blackdoctor.org

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