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DRUG DEVELOPMENT
PROCESS
Presented by krishna M 5th pharm d
• The entire process of taking a newly
compound or drug through regulatory
approval to the point of marketing.
• During the development, the new drug or the
compound should adhere to high standards in
the conduct, analysis and interpretation of
preclinical and clinical studies for its smooth
passage through the regulatory approval
phase and eventually to marketing. The drug
discovery and drug development process is
designed to ensure that only those
pharmaceutical products that are both safe
and effective are brought to market.
Add a Footer 2
INTRODUCTION
THE FOLLOWING
SEQUENCE OF
RESEARCH ACTIVITIES
BEGINS THE PROCESS
THAT RESULTS IN
DISCOVERY OF NEW
MEDICINES
• Target identification
• Target validation
• Lead identification
• Lead optimization
Add a Footer 3
DRUG DEVELOPMENT
PHASES
1. Pre-clinical research
and development
2. Clinical research and
development
3. After the compound is
on the market, a
possible “post
marketing” phase
Add a Footer 4
PRE-CLINICAL PHASE
• The pre-clinical studies represents bench
(in vitro) and then animal test, including
kinetics, toxicity and carcinogenicity. In
the us, an investigational new drug
application is submitted to food and drug
administration seeking permission to
begin the heavily regulated process of
clinical testing in human subjects. IND
phase representing the time from the
beginning of human trails to the new drug
application (NDA) submission that seeks
permission to market the drug is by far
the longest portion of the drug
development cycle and can last from 2
to10 years.
Add a Footer 5
PHASE I
• In this where the human trails
are generally conducted.
• Small group have 10-30 health
volunteer.
• Except for oncology or toxic
compounds.
• Small hospitals with 20-50 beds.
• Last for a day to 2 weeks and
even follow upto a month.
• Safety of the compound study
its pharmacokinetics and
pharmacodynamic.
Add a Footer 6
PHASE II
• Patient upto 300 patients
• Time duration few
months – years
• Efficacy of drug of
particular disease.
• Example – patient with
newly diagnosis but
untreated diabetes no
evidence of end organ
damage used to treat a
new antidiabetic agents.
Add a Footer 7

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Drug development process

  • 2. • The entire process of taking a newly compound or drug through regulatory approval to the point of marketing. • During the development, the new drug or the compound should adhere to high standards in the conduct, analysis and interpretation of preclinical and clinical studies for its smooth passage through the regulatory approval phase and eventually to marketing. The drug discovery and drug development process is designed to ensure that only those pharmaceutical products that are both safe and effective are brought to market. Add a Footer 2 INTRODUCTION
  • 3. THE FOLLOWING SEQUENCE OF RESEARCH ACTIVITIES BEGINS THE PROCESS THAT RESULTS IN DISCOVERY OF NEW MEDICINES • Target identification • Target validation • Lead identification • Lead optimization Add a Footer 3
  • 4. DRUG DEVELOPMENT PHASES 1. Pre-clinical research and development 2. Clinical research and development 3. After the compound is on the market, a possible “post marketing” phase Add a Footer 4
  • 5. PRE-CLINICAL PHASE • The pre-clinical studies represents bench (in vitro) and then animal test, including kinetics, toxicity and carcinogenicity. In the us, an investigational new drug application is submitted to food and drug administration seeking permission to begin the heavily regulated process of clinical testing in human subjects. IND phase representing the time from the beginning of human trails to the new drug application (NDA) submission that seeks permission to market the drug is by far the longest portion of the drug development cycle and can last from 2 to10 years. Add a Footer 5
  • 6. PHASE I • In this where the human trails are generally conducted. • Small group have 10-30 health volunteer. • Except for oncology or toxic compounds. • Small hospitals with 20-50 beds. • Last for a day to 2 weeks and even follow upto a month. • Safety of the compound study its pharmacokinetics and pharmacodynamic. Add a Footer 6
  • 7. PHASE II • Patient upto 300 patients • Time duration few months – years • Efficacy of drug of particular disease. • Example – patient with newly diagnosis but untreated diabetes no evidence of end organ damage used to treat a new antidiabetic agents. Add a Footer 7