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GENERIC LAUNCHES AND RISK
MITIGATION
Supriya Ramacha
Copyright 2012 BananaIP
Website: www.bananaip.com
Blog: www.bananaip.com/sinapse-blog
AGENDA
 Product launch
 Risks in product launch
 Risk mitigation strategies
PRODUCT LAUNCH -
GENERIC
PRODUCT LAUNCH
 Risk free route
Patent expiry
Work around
 At-risk route
Challenge/Infringe
RISKS IN PRODUCT
LAUNCHES
BACKGROUND
 Patent Rights
 Make
 Use
 Sell
 Offer for sale
 Import
 Territorial
 Term
PATENT RISKS
 Standard Patent Term
 Term extensions
Patent office delays
Regulatory delays
US-TERM EXTENSIONS
 Patent process-Patent term adjustments (PTA)
One day extension - every day delayed
Objective = 17 years
Types
A delays (failure to act-14-4-4-4 rule)
B delays (pendency beyond 3 years)
C delays (special situation)
EXAMPLE
 Billy owns a US patent application for a drug “X” filed
on Jan 1st
2002, for which he receives the first office
action on June 1st
2003. The patent is issued on Jan 1st
2005. Silly, a generic drug maker, wants to launch “Y,”
the generic version of the drug.
 Launch date?
 Bopi files a US patent application for a drug “Alpha”
filed on Jan 1st
1998, for which it receives the first
office action on June 1st
2000. The patent is issued on
Jan 1st
2005. Dopi, a generic drug maker, wants to
launch “Beta,” the generic version of the drug.
 PTA?
EXAMPLE
 Billy’s application for a drug “X” filed on Jan 1st
2002
receives the first office action on June 1st
2003.
 Billy’s patent is issued on March 1st
2007 after paying
the issue fee on Sept 1st
2006
 Silly’s Launch date ?
 Wyeth Vs Kappos case
PATENT TERM EXTENSIONS
 Regulatory process-Patent term extensions (PTE)
1/2 Testing phase + Approval phase
 Calculation
max of 5 years extension
NMT 14 years of potential marketing exclusivity
EXAMPLE
 Mandoz files for a US patent on “Mentos” on April 1st
2000. The patent is issued on July 1st
2002. It
subsequently files an IND application effective on July
1st
2003.
 Mandoz files an NDA on July 1st
2005 and receives
approval on July 1st
2006.
 Possible extension?
 Actual extension?
 Launch date?
PTEs depends on the no. of potential exclusive
marketing term available.
EXAMPLE
 Mandoz files for a US patent on “Mentos” on April 1st
2000. It files an IND application effective on July 1st
2002. The patent was issued on July 1st
2003.
 Mandoz files for an NDA on July 1st
2005 and receives
NDA approval on July 1st
2006.
 Possible extension?
 Actual extension?
 Launch date?
 Sprycel Tablets, Dasatinib,US6596746
PTE
 Calculation
Does not include anytime before the date of patent
issue
 Total patent term= Standard patent term + PTA + PTE
EUROPE
 Regulatory process- Supplementary protection
certificate (SPC)
SPC Term= (1st
MA date - patent filing date) - 5
years.
territorial
Calculation
5 years max (+6 months)
NMT 15 years of potential marketing exclusivity
 Total patent term = Standard Patent term + SPC
EXAMPLE
 Dizer, a French applicant, obtains a national
marketing approval on Jan 1st
2000, for a product
protected by a patent with the filing date of Jan 1st
1990.
 Dizer has also received a marketing approval in
Britain on Jan 1st
1997.
 Launch date?
EXAMPLE
 Banana & Co. files for a patent in France on Jan 1st
1998 for a drug “Todi” and receives a national
marketing approval on Jan 1st
2001. It also files for a
patent in Spain on Jan 1st
1999 and receives a
marketing approval in Spain on Jan 1st
2000.
 Launch date in France?
REGULATORY HURDLES IN
GENERIC LAUNCH
Copyright 2012 Brain League
REGULATORY HURDLES
 Regulatory exclusivities
Data exclusivity
Other exclusivity
US EXCLUSIVITIES
 Data exclusivity- 5 years
(+1.5 to 2 years)
 Other exclusivity-
New clinical study exclusivity-3 years
Orphan drug exlusivity-7 years
Pediatric exclusivity-6 months
EUROPE
 Currently- 6 or 10 years
(+1 to 3 years)
 New- 8+2+1 regime
 Current- (2001/83/EC Directive)
 New- (2001/83/EC Directive as amended by 2004/27/EC)
RISK MITIGATION
STRATEGIES
RISK MITIGATION STRATEGIES
 Risk free launches
Identify blocking patents- FTO analysis
Understanding expiry
 Infringement/ Challenging
Identify evidences – Invalidation
 Work around
Technology Landscaping
FTO ANALYSIS
Copyright 2012 Brain League
EVALUATE FTO
 Search
Patent databases-blocking patent/application
 Analysis
Infringement
ANALYSIS
 Infringement factors
Territorial
Term
Claims
TECHNOLOGY LANDSCAPE
ANALYSIS
©2011Intellecture
(www.intellectureindia.com)
TECHNOLOGY MAP
THANK YOU
FOR MORE DETAILS VISIT
WWW.BANANAIP.COM/SINAPSE-BLOG
A Property of BananaIP

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Generic Launches and Risk Mitigation

  • 1. GENERIC LAUNCHES AND RISK MITIGATION Supriya Ramacha Copyright 2012 BananaIP Website: www.bananaip.com Blog: www.bananaip.com/sinapse-blog
  • 2. AGENDA  Product launch  Risks in product launch  Risk mitigation strategies
  • 4. PRODUCT LAUNCH  Risk free route Patent expiry Work around  At-risk route Challenge/Infringe
  • 6. BACKGROUND  Patent Rights  Make  Use  Sell  Offer for sale  Import  Territorial  Term
  • 7. PATENT RISKS  Standard Patent Term  Term extensions Patent office delays Regulatory delays
  • 8. US-TERM EXTENSIONS  Patent process-Patent term adjustments (PTA) One day extension - every day delayed Objective = 17 years Types A delays (failure to act-14-4-4-4 rule) B delays (pendency beyond 3 years) C delays (special situation)
  • 9. EXAMPLE  Billy owns a US patent application for a drug “X” filed on Jan 1st 2002, for which he receives the first office action on June 1st 2003. The patent is issued on Jan 1st 2005. Silly, a generic drug maker, wants to launch “Y,” the generic version of the drug.  Launch date?
  • 10.  Bopi files a US patent application for a drug “Alpha” filed on Jan 1st 1998, for which it receives the first office action on June 1st 2000. The patent is issued on Jan 1st 2005. Dopi, a generic drug maker, wants to launch “Beta,” the generic version of the drug.  PTA?
  • 11. EXAMPLE  Billy’s application for a drug “X” filed on Jan 1st 2002 receives the first office action on June 1st 2003.  Billy’s patent is issued on March 1st 2007 after paying the issue fee on Sept 1st 2006  Silly’s Launch date ?  Wyeth Vs Kappos case
  • 12. PATENT TERM EXTENSIONS  Regulatory process-Patent term extensions (PTE) 1/2 Testing phase + Approval phase  Calculation max of 5 years extension NMT 14 years of potential marketing exclusivity
  • 13. EXAMPLE  Mandoz files for a US patent on “Mentos” on April 1st 2000. The patent is issued on July 1st 2002. It subsequently files an IND application effective on July 1st 2003.  Mandoz files an NDA on July 1st 2005 and receives approval on July 1st 2006.  Possible extension?  Actual extension?  Launch date?
  • 14. PTEs depends on the no. of potential exclusive marketing term available.
  • 15. EXAMPLE  Mandoz files for a US patent on “Mentos” on April 1st 2000. It files an IND application effective on July 1st 2002. The patent was issued on July 1st 2003.  Mandoz files for an NDA on July 1st 2005 and receives NDA approval on July 1st 2006.  Possible extension?  Actual extension?  Launch date?  Sprycel Tablets, Dasatinib,US6596746
  • 16. PTE  Calculation Does not include anytime before the date of patent issue  Total patent term= Standard patent term + PTA + PTE
  • 17. EUROPE  Regulatory process- Supplementary protection certificate (SPC) SPC Term= (1st MA date - patent filing date) - 5 years. territorial Calculation 5 years max (+6 months) NMT 15 years of potential marketing exclusivity  Total patent term = Standard Patent term + SPC
  • 18. EXAMPLE  Dizer, a French applicant, obtains a national marketing approval on Jan 1st 2000, for a product protected by a patent with the filing date of Jan 1st 1990.  Dizer has also received a marketing approval in Britain on Jan 1st 1997.  Launch date?
  • 19. EXAMPLE  Banana & Co. files for a patent in France on Jan 1st 1998 for a drug “Todi” and receives a national marketing approval on Jan 1st 2001. It also files for a patent in Spain on Jan 1st 1999 and receives a marketing approval in Spain on Jan 1st 2000.  Launch date in France?
  • 20. REGULATORY HURDLES IN GENERIC LAUNCH Copyright 2012 Brain League
  • 21. REGULATORY HURDLES  Regulatory exclusivities Data exclusivity Other exclusivity
  • 22. US EXCLUSIVITIES  Data exclusivity- 5 years (+1.5 to 2 years)  Other exclusivity- New clinical study exclusivity-3 years Orphan drug exlusivity-7 years Pediatric exclusivity-6 months
  • 23. EUROPE  Currently- 6 or 10 years (+1 to 3 years)  New- 8+2+1 regime  Current- (2001/83/EC Directive)  New- (2001/83/EC Directive as amended by 2004/27/EC)
  • 24.
  • 26. RISK MITIGATION STRATEGIES  Risk free launches Identify blocking patents- FTO analysis Understanding expiry  Infringement/ Challenging Identify evidences – Invalidation  Work around Technology Landscaping
  • 28. EVALUATE FTO  Search Patent databases-blocking patent/application  Analysis Infringement
  • 31.
  • 34. THANK YOU FOR MORE DETAILS VISIT WWW.BANANAIP.COM/SINAPSE-BLOG A Property of BananaIP