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DR ANTHONY M CRASTO (Ph.D) PRINCIPAL SCIENTIST PROCESS RESEARCH DEC 2011 “ A SHORT PRESENTATION”
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Net Cost: $802 Million  Invested Over 15 Years  5,000–10,000 Screened 250 Enter Preclinical Testing 5 Enter Clinical Testing 1 Compound Success  Rates by Stage 16 14 12 10 8 6 4 2 0 Phase II 100–300 Patient Volunteers Used to Look for Efficacy  and Side Effects Phase III 1,000–5,000 Patient Volunteers Used to Monitor Adverse Reactions to Long-Term Use FDA Review Approval Additional Post-Marketing Testing Phase I  20–80 Healthy Volunteers Used to Determine Safety and Dosage Preclinical Testing Laboratory and Animal Testing Discovery (2–10 Years) Years New Product Development –  A Risky and Expensive Proposition Approved by the FDA
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Med Chem Clinical  Chem E R&D Pharm  R&D Safety Analytical Process
responsible for developing In-process assay and critical evaluation of  drug substance and intermediates Med Chem Clinical  Chem E R&D Pharm  R&D Safety Analytical Process
responsible for toxicity studies:  (carcinogen, teratogen, gene toxicity ) Med Chem Clinical  Chem E R&D Pharm  R&D Safety Analytical Process
responsible for formulating drug substance (API) into drug product Med Chem Clinical  Chem E R&D Pharm  R&D Safety Analytical Process
Oversee process transfer into Pilot plants Med Chem Clinical  Chem E R&D Pharm  R&D Safety Analytical Process
Conducts clinical trials  (Ph I-III) and evaluates data Med Chem Clinical  Chem E R&D Pharm  R&D Safety Analytical Process
Discovers new chemical  entities (NCE’s) and  prepares intitial quantities Med Chem Clinical  Chem E R&D Pharm  R&D Safety Analytical Process
[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
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[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object]
Selective Dopamine-2 Antagonist Indication: Anti-psychotic (Depression/Schizophrenia) Clinical Trials: halted in 1993 due to anemia side-effects
 
 
Auerbach, Weissman  Tet Letters   1993,  931
 
Drawbacks: 1. Use of costly Oxalyl Chloride 2. CO and CO 2  by-products 3. Lengthy time cycle due to exothermic amination reaction 4. Need for 3 equiv of volatile  t -butylamine 5. Filtration/Disposal of voluminous amine hydrochloride salt
 
A: 179/[124+127+73+73]  = 45 % B: 179/[105 + 98 +74 +18] = 61%
 
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Process research overview

  • 1. DR ANTHONY M CRASTO (Ph.D) PRINCIPAL SCIENTIST PROCESS RESEARCH DEC 2011 “ A SHORT PRESENTATION”
  • 2.
  • 3. Net Cost: $802 Million Invested Over 15 Years 5,000–10,000 Screened 250 Enter Preclinical Testing 5 Enter Clinical Testing 1 Compound Success Rates by Stage 16 14 12 10 8 6 4 2 0 Phase II 100–300 Patient Volunteers Used to Look for Efficacy and Side Effects Phase III 1,000–5,000 Patient Volunteers Used to Monitor Adverse Reactions to Long-Term Use FDA Review Approval Additional Post-Marketing Testing Phase I 20–80 Healthy Volunteers Used to Determine Safety and Dosage Preclinical Testing Laboratory and Animal Testing Discovery (2–10 Years) Years New Product Development – A Risky and Expensive Proposition Approved by the FDA
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14. Med Chem Clinical Chem E R&D Pharm R&D Safety Analytical Process
  • 15. responsible for developing In-process assay and critical evaluation of drug substance and intermediates Med Chem Clinical Chem E R&D Pharm R&D Safety Analytical Process
  • 16. responsible for toxicity studies: (carcinogen, teratogen, gene toxicity ) Med Chem Clinical Chem E R&D Pharm R&D Safety Analytical Process
  • 17. responsible for formulating drug substance (API) into drug product Med Chem Clinical Chem E R&D Pharm R&D Safety Analytical Process
  • 18. Oversee process transfer into Pilot plants Med Chem Clinical Chem E R&D Pharm R&D Safety Analytical Process
  • 19. Conducts clinical trials (Ph I-III) and evaluates data Med Chem Clinical Chem E R&D Pharm R&D Safety Analytical Process
  • 20. Discovers new chemical entities (NCE’s) and prepares intitial quantities Med Chem Clinical Chem E R&D Pharm R&D Safety Analytical Process
  • 21.
  • 22.
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29. Selective Dopamine-2 Antagonist Indication: Anti-psychotic (Depression/Schizophrenia) Clinical Trials: halted in 1993 due to anemia side-effects
  • 30.  
  • 31.  
  • 32. Auerbach, Weissman Tet Letters 1993, 931
  • 33.  
  • 34. Drawbacks: 1. Use of costly Oxalyl Chloride 2. CO and CO 2 by-products 3. Lengthy time cycle due to exothermic amination reaction 4. Need for 3 equiv of volatile t -butylamine 5. Filtration/Disposal of voluminous amine hydrochloride salt
  • 35.  
  • 36. A: 179/[124+127+73+73] = 45 % B: 179/[105 + 98 +74 +18] = 61%
  • 37.  
  • 38.
  • 39.
  • 40.
  • 41.
  • 42.

Notas del editor

  1. Regulatory- talk of CMC (“chemistry and manufacturing controls”) section