1 / 26

The Pharmaceutical Industry and The Process of Drug Discovery

The Pharmaceutical Industry and The Process of Drug Discovery. What is a Drug? Types of Pharmaceutical Products What are the Important Disease Targets? How the Industry Has Evolved Drug Discovery and The Process of Getting a Drug to Market - an overview. What is a drug?.

pearly
Download Presentation

The Pharmaceutical Industry and The Process of Drug Discovery

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. The Pharmaceutical Industry and The Process of Drug Discovery • What is a Drug? • Types of Pharmaceutical Products • What are the Important Disease Targets? • How the Industry Has Evolved • Drug Discovery and The Process of Getting a Drug to Market - an overview

  2. What is a drug? “A Chemical Substance that Interacts with a Living System and Produces a Biological Response”

  3. What is a drug? “A Chemical Substance that Interacts with a Living System and Produces a Biological Response”

  4. What is a drug? “A Chemical Substance that Interacts with a Living System and Produces a Biological Response” • Good and Bad Drugs? • Safe Drugs?

  5. What is a drug? “A Chemical Substance that Interacts with a Living System and Produces a Biological Response” • Good and Bad Drugs? • Safe Drugs? Morphine (bad?)vs.penicillin (good?) Curare vs. paracetamol

  6. Classification of Drug Types • Ethical drugs • Generic drugs (no longer under patent) • “Prescription Only” vs “Over the Counter” • “Off Label” applications • Orphan drugs • Biotechnology products • Counterfeit drugs • Street drugs!

  7. What criteria MUST new drugs meet? • Drugs must address a new need or provide a significant “added benefit” over an existing medicine • Drugs must also meet five criteria: • Must be safe, effective, of high quality • …cost effective (1980s) • ……….affordable (1990s) • ……………REALLY affordable (2000+)

  8. Major Therapeutic Targets • Infectious disease – anti-infectives • Anti-bacterial, anti-viral, anti-parasitic drugs • Metabolic disease • cancer, cardiovascular, diabetes,inflammation, high blood pressure, neurological disease, pain • Other aspects of health care • Hormonal treatments, contraception, vaccines, immunosuppresents, anaesthetics, nutraceuticals, “life style” drugs

  9. A History of the Pharmaceutical Industry • The early days - Egyptians, Greeks, Arabs, China, India • Plant-derived medicines • morphine (1805), quinine (1819), colchicine (1820), pilocarpine (1875) • Hormones • insulin (1921), estradiol (1929), testosterone (1931), “the pill” (1960) • Antibiotics, Psychoactive drugs (post-1945 to 1960’s) • penicillin (1944), streptomycin (1944), valium (1963) • Treatment of metabolic disorders (1960’s to current day) • Ventolin (1969), Lipitor (1997), Viagra (1998), Avandia (1999), Vioxx (1999), Gleevec (2001) • Search for gene therapies (1990), stem cell-based therapies • Stem-cell replacement of a trachea (2008)

  10. Some Important Events • American Civil War • Legislation – UK Cruelty to Animals Act (1876); US Federal Food and Drug Act (1906) • World War 1 - Development of UK regulatory rules • World War 2 – antibiotics • Vaccines – Smallpox: Jenner (1796) – eradicated in 1977 • Thalidomide (1960) – report adverse drug reactions • AIDS (1980s) – fast track approval, “buyer power” • Viagra (1998) • Tamiflu – H1N1 (swine flu) pandemic (2009) • NICE (1999) – the affordability factor • Vioxx – anti-inflammatory – 1999-2004 due to litigation • Avandia – Type 2 (non-insulin dependent) diabetes - 1999-2010 also due to litigation

  11. How do drugs work? • The Biological Target - enzyme or receptor • Where is the target - part of “us” or elsewhere • Paul Ehrlich, Nobel Prize 1908, salvarsan; • blood-brain barrier; “Lock and Key” hypothesis; chemotherapy and “magic bullet” The Lock - Active Site of Enzyme/Receptor The Key - the Drug

  12. The “Lock and Key” analogy Key Lock Binding • Here the KEY is the natural substrate • Binding of the KEY to the LOCK (an enzyme or a receptor) then causes a response – a shape change in the protein/receptor

  13. The “Lock and Key” analogy Key Lock Binding Biological Response • Here the KEY is the natural substrate • Binding of the KEY to the LOCK (an enzyme or a receptor) then causes a response – a shape change in the protein/receptor

  14. Biological response is altered OR shut down But when an effective drug is present vs. Binding of Drug is preferred • Drug may bind preferentially to the “active site” • Antagonist – binds and BLOCKS • Agonist – binds and ACTIVATES • Partial agonist – induces a partial response

  15. Who discovers drugs? Doctors? • Identify biological target - biology • Prioritise/ validate target – pharmacology and chemistry • Identify and optimise lead molecules – chemistry/pharmacology • Preclinical studies – chemistry/pharmacology/ toxicology • Formulation - pharmaceutical sciences • Clinical evaluation – medicine • Manufacture - chemical engineering

  16. Getting a drug to market • Disease target - possible drug candidates • Pre-clinical testing; R&D (1-3 yrs) • Toxicology, “ADME” • Clinical R&D (2-10 yrs; Av. 5yrs) • Phase 1 – healthy volunteers • Phase 2 – small patient group • Phase 3 – larger patient group • Regulatory approval (2-10(!) yrs) • Market • Phase 4 – long term monitoring

  17. The Gamble - wastage and timescale • For EACHDRUGapproved, an average of 7500 compounds will have been made • Of this 7500, anaverage of 21 will be tested for subacute toxicology, 6.5 will be tested in humans and 2.5 will reach Phase 3 – 1 then gets to market……… • Entire process takes onaverage 12 years • Costs $138M (1975); $800M (2000); $1.6Bn (2008) • Development costs do NOT include pre-launch marketing which can DOUBLE costs

  18. The “Pay Off”……to the companies • Typical R&D budget: 33% R and 67%D • R&D = 15 to 25 % of sales turnover • Patent protection – 20 years from filing • On average, 11yrs. of productive market life • Losec – $2.7Bn in 1998; Nexium (single enantiomer) $7.7Bn in 2008 • Lipitor - $1Bn in 1998; $13.8Bn in 2008

  19. The “Pay Off”…….to us • Massive contributions to health, quality of life, reduced child mortality, life expectancy • Vaccines have eradicated major disease – smallpox; vaccines for malaria and pneumonia soon……..? • But costs and accessibility to healthcare are becoming major social and geopolitical issues • And, is there something seedy about making money out of illness? • What will happen into the future?

  20. The Companies in 2010

  21. Major Therapeutic Targets

  22. Top 10 Therapies - sales in 2008 (US$Bn)

  23. What makes a good drug? Lipinski's rules (Chris Lipinski – 1997) In general, an orally active drug will meet most of the following: • Not more than 5 hydrogen bond donors (nitrogen or oxygen atoms with one or more hydrogen atoms) • Not more than 10 hydrogen bond acceptors (nitrogen or oxygen atoms) • A molecular weight under 500 daltons • An octanol-water partition coefficient log P of less than 5 • http://www.molinspiration.com/cgi-bin/properties

  24. US UK Into volunteers Cimetidine Burimamide First lead Programme starts Case Study Cimetidine (Tagamet) 1979 • H2 blocker; anti-ulcer/heartburn • 1983 First drug to reach $1Bn • Cleared for OTC in 1995 1976 1974 1972 1970 1968 1966 1964

  25. What is a drug? “A Chemical Substance that Interacts with a Living System and Produces a Biological Response”

More Related