SlideShare a Scribd company logo
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Finding and Evaluating
Branded and Generic
Market Entry Opportunities
YALI FRIEDMAN, PH.D.
ADMIN@DRUGPATENTWATCH.COM
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Outcomes
 Be a value-added partner for your branded and
generic clients
 Anticipate generic entry so you can prepare for
changes in demand
 Find and evaluate generic entry opportunities
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
More generics = lower prices
Source: FDA
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
API volume increases after patent expiration
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Factors influencing generic entry decisions
Ingredient Recipe and Testing Capital Distribution
Effect
Size
Large Medium Large Medium
Reason Trusted
suppliers
Compound
properties
known
Experience with
form, family, and
ingredient reduces
research
expenditure
Experience with
form reduces
development
cost
Reduces effort
to find
customers
Source: M. Scott Morton, Fiona. (1999). Entry Decisions in the Generic
Pharmaceutical Industry. RAND Journal of Economics. 30. 421-440.
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Strong generic first-mover advantage
 1st generic can enjoy 80% market share advantage over 2nd entrant
 Advantage can last for years
Why?
 Supplier decisions based on price, reputation, and recall history
 Switching can introduce inventorying costs
Costs of switching suppliers may favor first entrant
Source: Yu, Y., Gupta S. Pioneering Advantage in Generic Drug Competition International Journal of Pharmaceutical and Healthcare Marketing
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Use sales to track demand for drug / category
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Branded vs. generic price may indicate competition
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Brand and generic may use different channels
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Find 505(b)(2) opportunities
New Drug
NDA / 505(b)(1)
Generic Drug
ANDA / 505(j)
Hybrid
505(b)(2)
Contains full reports of
investigations of safety and
effectiveness that were
conducted by or for the
applicant or for which the
applicant has a right of
reference or use.
Relies on FDA’s finding that
a previously approved
reference listed drug is safe
and effective ... May not be
submitted if clinical
investigations are necessary
to establish the safety and
effectiveness of the
proposed drug product.
Contains full reports of
investigations of safety and
effectiveness, where at least
some of the information
required for approval
comes from studies not
conducted by or for the
applicant and for which the
applicant has not obtained a
right of reference or use.
Source: FDA
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Most common 505(b)(2) types
New formulation or manufacturer 43%
New dosage form 29%
New combination 13%
Source: Freije, I., Lamouche, S., & Tanguay, M. (2019). Review of Drugs Approved via the 505(b)(2) Pathway: Uncovering
Drug Development Trends and Regulatory Requirements. Therapeutic Innovation & Regulatory Science.
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Increase client affinity with authorized generics
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Generic drug types
Branded Generic Authorized Generic Traditional Generic
Approval Process ANDA or 505(b)(2) NDA ANDA
Relation to
patent expiration
Sold after patent
expiration
Can be sold before
patent expiration
Sold after drug
patent expiration
Cost Typically more
than unbranded
generic; less than
branded drug
Typically more
than unbranded
generic; less than
branded drug
Typically less
than branded or
authorized
generics
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Branded generics
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Patent claim types
• If a patent claims the active ingredient it may be impossible to work around
Compound claims
• If a generic entrant can work around a patented production process they may
be able to launch
Process claims
• Patents on specific formulations / dosage forms (e.g. transdermal patch or
autoinjector) do not protect they active ingredient
Formulation / Dosage claims
• If a drug has multiple uses, a generic may launch for unpatented indications
using a skinny label
Use claims
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Patent priority cheat-sheet
Extended patents
Litigated patents
Compound-claiming patents
Unexpired patents
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Finding low-competition opportunities
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Fast-follower: Day-181 Launch
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Get intel from patent litigation
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
$2.3mm to defend patent
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
25% Royalty
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
How much was earned?
$100mm royalty payments over 2y implies $200mm/yr in generic sales
💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
Thank You
Yali Friedman, Ph.D.
admin@DrugPatentWatch.com
www.drugpatentwatch.com/make-better-decisions/

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Finding and evaluating branded and generic market entry opportunities

  • 1. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Finding and Evaluating Branded and Generic Market Entry Opportunities YALI FRIEDMAN, PH.D. ADMIN@DRUGPATENTWATCH.COM
  • 2. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Outcomes  Be a value-added partner for your branded and generic clients  Anticipate generic entry so you can prepare for changes in demand  Find and evaluate generic entry opportunities
  • 3. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com More generics = lower prices Source: FDA
  • 4. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com API volume increases after patent expiration
  • 5. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Factors influencing generic entry decisions Ingredient Recipe and Testing Capital Distribution Effect Size Large Medium Large Medium Reason Trusted suppliers Compound properties known Experience with form, family, and ingredient reduces research expenditure Experience with form reduces development cost Reduces effort to find customers Source: M. Scott Morton, Fiona. (1999). Entry Decisions in the Generic Pharmaceutical Industry. RAND Journal of Economics. 30. 421-440.
  • 6. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Strong generic first-mover advantage  1st generic can enjoy 80% market share advantage over 2nd entrant  Advantage can last for years Why?  Supplier decisions based on price, reputation, and recall history  Switching can introduce inventorying costs Costs of switching suppliers may favor first entrant Source: Yu, Y., Gupta S. Pioneering Advantage in Generic Drug Competition International Journal of Pharmaceutical and Healthcare Marketing
  • 7. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Use sales to track demand for drug / category
  • 8. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Branded vs. generic price may indicate competition
  • 9. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Brand and generic may use different channels
  • 10. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Find 505(b)(2) opportunities New Drug NDA / 505(b)(1) Generic Drug ANDA / 505(j) Hybrid 505(b)(2) Contains full reports of investigations of safety and effectiveness that were conducted by or for the applicant or for which the applicant has a right of reference or use. Relies on FDA’s finding that a previously approved reference listed drug is safe and effective ... May not be submitted if clinical investigations are necessary to establish the safety and effectiveness of the proposed drug product. Contains full reports of investigations of safety and effectiveness, where at least some of the information required for approval comes from studies not conducted by or for the applicant and for which the applicant has not obtained a right of reference or use. Source: FDA
  • 11. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Most common 505(b)(2) types New formulation or manufacturer 43% New dosage form 29% New combination 13% Source: Freije, I., Lamouche, S., & Tanguay, M. (2019). Review of Drugs Approved via the 505(b)(2) Pathway: Uncovering Drug Development Trends and Regulatory Requirements. Therapeutic Innovation & Regulatory Science.
  • 12. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Increase client affinity with authorized generics
  • 13. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Generic drug types Branded Generic Authorized Generic Traditional Generic Approval Process ANDA or 505(b)(2) NDA ANDA Relation to patent expiration Sold after patent expiration Can be sold before patent expiration Sold after drug patent expiration Cost Typically more than unbranded generic; less than branded drug Typically more than unbranded generic; less than branded drug Typically less than branded or authorized generics
  • 14. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Branded generics
  • 15. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Patent claim types • If a patent claims the active ingredient it may be impossible to work around Compound claims • If a generic entrant can work around a patented production process they may be able to launch Process claims • Patents on specific formulations / dosage forms (e.g. transdermal patch or autoinjector) do not protect they active ingredient Formulation / Dosage claims • If a drug has multiple uses, a generic may launch for unpatented indications using a skinny label Use claims
  • 16. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Patent priority cheat-sheet Extended patents Litigated patents Compound-claiming patents Unexpired patents
  • 17. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Finding low-competition opportunities
  • 18. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Fast-follower: Day-181 Launch
  • 19. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com
  • 20. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Get intel from patent litigation
  • 21. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com $2.3mm to defend patent
  • 22. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com 25% Royalty
  • 23. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com How much was earned? $100mm royalty payments over 2y implies $200mm/yr in generic sales
  • 24. 💊 DrugPatentWatch.com #MAKEBETTERDECISIONS ✉ admin@DrugPatentWatch.com Thank You Yali Friedman, Ph.D. admin@DrugPatentWatch.com www.drugpatentwatch.com/make-better-decisions/