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Introduction To Clinical Trial

Clinical research determines the safety and effectiveness of medical treatments and involves systematic clinical trials on human subjects. [1] The clinical trial process can take over 14 years on average and involves testing in phases to gain approval. [2] Participants in clinical trials help advance medical research and future treatments by contributing to our scientific knowledge of diseases. [3]

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328 views

Introduction To Clinical Trial

Clinical research determines the safety and effectiveness of medical treatments and involves systematic clinical trials on human subjects. [1] The clinical trial process can take over 14 years on average and involves testing in phases to gain approval. [2] Participants in clinical trials help advance medical research and future treatments by contributing to our scientific knowledge of diseases. [3]

Uploaded by

upendernathi
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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➢ Clinical Research is a branch of healthcare

science that determines the safety and effectiveness


(efficacy) of medications, devices, diagnostic
products and treatment regimens intended for
human use. These may be used for prevention,
treatment, diagnosis or for relieving symptoms of a
disease.
SAFE
➢ Clinical Trial

• A clinical trial is a systematic investigation in human subjects for evaluating the


safety and efficacy of new drug.
.
• The time from drug discovery to marketing takes an average of 14 years.

• The data obtained from the first-time-in-human, Phase 1 pharmacokinetic


studies and initial safety evaluation in healthy volunteers can make or break the
entire development program for a drug candidate

• Goal is to gain approval to market the drug, which requires a marketing


application be submitted to regulatory agencies.

• A critical function is the development of the study protocol which must clearly
describe the study design and methodology that applied to achieve the study
objectives.
• Clinical trial is the mainstay for bringing out new drugs to the market.
• Medical and behavioral research involving volunteer participants
• Investigations that are carefully developed and conducted with clinical
outcomes recorded
• Strict scientific guidelines
• Ethical principles to protect participants .
➢ Why participate in a clinical trial?

Because clinical trials are required of any new therapy prior to FDA
approval, major improvements in health care would be impossible
without volunteer participants. Participants in clinical trials can play a
more active role in their own health care, gain access to new research
treatments before they are widely available, and help others by
contributing to medical research.
➢ Why is clinical Research Important (Benefits)?

Research is important because:

• Clinical trials test how well new approaches and interventions work in people

• These approaches can be medical, behavioral, or management

• Each study answers scientific questions

• Each study helps scientists prevent, screen for, diagnose, manage, and treat a
disease .

People who take part in clinical trials contribute to the knowledge of how a
disease progresses.
➢ Who can participate in a clinical trial?

• All clinical trials have guidelines about who can participate. The factors
that allow someone to participate in a clinical trial will vary from study to
study.
• These criteria are based on the goals of the study and include such factors
as age, the type and stage of a disease, previous treatment history, and other
medical conditions.
• The main goal for using volunteers in a clinical trial is to prove, by
scientific means, the effects and limitations of the experimental treatment
on a wide variety of people.
What Are Inclusion/Exclusion Criteria?

All clinical trials have guidelines about who can participate—these are specified in
the inclusion/exclusion criteria:

• Factors that allow someone to participate in a clinical trial are "inclusion criteria"
• Factors that exclude or do not allow participation in a clinical trial are "exclusion
criteria"
These factors may include:
• Age
• Gender
• The type and stage of a disease
• Previous treatment history
• Specific lab values
• Other medical conditions
Inclusion and exclusion criteria are not used to reject people personally. The criteria
are used to:
• Identify appropriate participants
• Keep them safe
• Help ensure that researchers can answer the questions they want answered
Where Do Clinical Trials Take Place?

Clinical trials take place all over the world:

• Medical centers
• Private and government hospitals and clinics
Clinical trials may include participants at one or two highly specialized centers. Or
they may Involve hundreds of locations at the same time.

What Are Some of the Possible Risks Associated with Taking Part in a
Clinical Trial?

Some risks of taking part in a clinical trial are:


• New vaccines and other strategies under study are not always better than the
standard care to which they are being compared
• New treatments may have unexpected side effects or risks that are worse than
those resulting from standard care
What Is the Clinical Research Process?

The clinical research process includes:


• Pre-clinical testing
• Investigational New Drug Application (IND)
• Phase I (assess safety)
• Phase II (test for effectiveness)
• Phase III (large-scale testing)
• Licensing (approval to use)
• Approval (available for prescription)
• Post-marketing studies (special studies and long-term
effectiveness/use)

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