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The Case For Naming Sooner
…Than Later
April 15, 2015
Draft Presentation for BIO, 2015
Bill Smith, CEO
Brand Acumen, LLC
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
In March, 2015, a study of 79 pharmaceutical
naming and trademark professionals was
conducted by BrandAcumen.
The purpose of the study was to define
challenges and trends in the drug naming
process.
The key findings …
The Research:
Pharmaceutical Naming Impact Study
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
Drug companies are developing trademarks for
new products at an earlier stage of development
in an effort to entrench a brand in the minds of
HCPs, BioJournalists, Potential Patients,Affinity
Proponents,Academia and the Financial
Community.
The Research:
Pharmaceutical Naming Impact Study
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
The overwhelming majority of the
professionals surveyed in the study stated
that they develop generic and trademark
names, 91% and 87% respectively, before
or during Phase II of clinical trials.
The Research:
Pharmaceutical Naming Impact Study
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
The outcome of the study recommends
seeking a trademark early — even during
Phase I — as trademark searches have a
low success rate.
This fast movement is even more important
for compounds with Expedited FDAReview
Programs, Oncology, Orphan Drug, Cell and
Gene Therapy Submissions.
The Research:
Pharmaceutical Naming Impact Study
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
Moreover, the study suggests drug companies
identify empty vessel names along with
suggestive names, arguing that empty-vessel
names can be easy to identify, protect and
re-use.
In addition, they pose less of a risk for rejection
under medical error recognition evaluation or
for conflicting with clinical trials results.
The Research:
Pharmaceutical Naming Impact Study
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
The Survey Overview
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
U.S.External TM Counsel (12)
U.S. Internal (Company) TM Counsel (17)
Chief Medical Officer (9)
Regulatory (Internal) (14)
Regulatory (Government) International (7)
Commercialization/Launch Directors (20)
Sample Profile Of Survey Respondents
Total Respondents
79
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
U.S.External TM Counsel (12)
U.S. Internal (Company) TM Counsel (17)
Chief Medical Officer (9)
Regulatory (Internal) (14)
Regulatory (Government) International (7)
Commercialization/Launch Directors (20)
Question:
Compared to this time last year, do you
feel compelled to begin the naming
process earlier in the drug development
cycle due to increased obstacles in
clearing a name?
10 of 12
13 of 17
6 of 9
9 of 14
4 of 7
17 of 20
TheResearchResults:
PharmaceuticalNamingImpactStudy
The ‘Yes’ Responses
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
U.S.External TM Counsel (12)
U.S. Internal (Company) TM Counsel (17)
Chief Medical Officer (9)
Regulatory (Internal) (14)
Regulatory (Government) International (7)
Commercialization/Launch Directors (20)
Question:
Do you believe that general costs
associated with naming have
escalated from two (2) years ago?
9 of 12
14 of 17
5 of 9
13 of 20
4 of 7
7 of 14
TheResearchResults:
PharmaceuticalNamingImpactStudy
The ‘Yes’ Responses
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
U.S.External TM Counsel (12)
U.S. Internal (Company) TM Counsel (17)
Chief Medical Officer (9)
Regulatory (Internal) (14)
Regulatory (Government) International (7)
Commercialization/Launch Directors (20)
Question:
Do you believe that the growing
number of FDA naming
submissions has caused a
slowdown in the review process
over the past two (2) years?
TheResearchResults:
PharmaceuticalNamingImpactStudy
The ‘Yes’ Responses
10 of 12
13 of 17
6 of 9
9 of 14
4 of 7
17 of 20
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
The New Factors Impacting Naming
BrandAcumen
“The Global Leader in Pharmaceutical Name Development and Submissions”
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
bioarbitrage
In the BioArbitrage Fund, the
business model acquires early stage
assets (compounds), then quickly
repackages and embellishes the
asset for divestiture.
By creating a brand name at Pre-
Clinical/ Phase I development, the
fund amplifies the ROI prior to
‘flipping the asset’ (divesting) to an
acquirer.
Identification of Asset (Pre-Clinical or Phase I)
Negotiate Terms of Option Agreement with Seller
Brand the Asset. Name, Design, Positioning, etc.
.
Create Offering Memorandum for Divestiture
Market Asset to Potential Acquirers
Close Transaction Triggering The Option
Resulting in net ‘delta’ gain (arbitrage)
BioArbitrage Process
Early Stage Naming
•  Pre-Clinical
•  Phase I
EmergingNewBusinessModelsareDrivingEarlyStage
NameDevelopment
thearbitrageimpact
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
An orphan drug accelerator focused on
developing and delivering life-transforming
therapies for patients with severe and life-
threatening rare diseases.
Orphanetics is privately funded by public and
private investors from the pharmaceutical, life
sciences and global healthcare community.
orphanetics
Orphanetics engages in:
•  Early Stage Naming of Clinical Programs
•  Non-Proprietary Name Development
•  Proprietary Name Development
•  EPC Naming
•  New Disease Branding •  MultiModal Orphan Drug Class
•  Infinitive Phenoptics
•  Vektür Micro Orphan Designation
•  Harlequin Gan Syndrome
•  Terracon SoSai Disorder
EmergingNewBusinessModelsareDrivingEarlyStage
NameDevelopment
therarediseasebio-accelerator
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
@earlybranding=enhancedvaluation
Lentiglobin®
Lenti-D®
StarbeamStudy
NorthStarStudy
branded clinical studies
pipeline
product brands
Newly minted
public
companies are
branding early ;
not just the
product pipeline,
but also their
clinical studies.
Branding
enhances
valuation, leading
to access to
financial
resources for
acquisitions
…and
partnerships
EmergingNewBusinessModelsareDrivingEarlyStage
NameDevelopment
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
EmergingNewBusinessModelsareDrivingEarlyStage
ProprietaryNameDevelopment
The dawn of ‘Name Repositories’ which own a
broad portfolio of pharmaceutical and life
science trademarks, service marks, platform
identifiers, disease state nomenclature and
domain names is the next wave indicator of the
value of names as an intellectual property asset.
These repositories operate as IP estates with a
focus on capturing value in nomenclature as an
asset.
Emergence of Private Pharmaceutical
Name Repositiories
Structured around the concept of
Microsoft Co-Founder Nathan Myhrvold’s
Intellectual Ventures, this new breed of
‘name bank’ is creating a greater need to
capture naming assets early.
thenewbankers
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
•  CAR-T
•  GeneTherapy
•  CRISPR
Companies benefit from early stage naming as
first to market leaders in their respective fields.
Additionally, as these companies seek strategic
partners and funding, brands become assets,
which in turn enhance valuations.
New Drug Technology Platforms
SleepingBeauty
RheoSwitch®
ZIOPHARM
platformbrands
AttSite®
UltraVector®
LEAP®
In the case of ZIOPHARM, brand recognition can also
be key to securing pivotal strategic and financial
partnerships.
investment
newplatform
earlystagebrands
EmergingNewBusinessModelsareDrivingEarlyStage
ProprietaryNameDevelopment
earlierstagenaming
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
EarlierNamingBehavior
18	
  
As a result of a greater
number of sponsors
participating in the FDA’s
Expedited Review Programs,
the proliferation of name
candidate submissions has
created a strain on FDA
resources for naming reviews.
FDA’sExpeditedReviewPrograms
Breakthrough
Designation
Accelerated
Approval
Fast Track
Designation
Priority
Review
The byproduct is that
companies are
beginning the naming
process earlier to
ensure approvals
through the parallel
channels of the FDA
and PTO
moreandmorenamesubmissions
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
In the case of emerging drug discovery platforms, securing the first non-proprietary
designation can also prove beneficial as competitors may be compelled to adopt variants
of the nomenclature in their USAN filings.
tisagenlecleucel-T
tisa – gen – lec – leu – cel - T
generic name
non-proprietary name
thenon-proprietaryadvantage EmergingNewBusinessModelsareDrivingEarlyStage
Non-ProprietaryNameDevelopment AsWell
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
TheResearchResults:
PharmaceuticalNamingImpactStudy
CAR-T
anewlexicon
Next generation
technology platforms
birth entire new lexicons
overnight.
With this, one must also
consider the
implications of the entire
framework of the
healthcare ecosystem
when selecting name
candidates.
newlexicons:moreconfusion
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
Factors Driving Early Stage Proprietary Naming
•  In the case of rare diseases and high profile unmet needs (liver ,
pancreatic cancers, etc.), drug companies are recognizing the
benefits of branding early to secure top of mind recognition sooner
than later.
•  Compliance with FDA and PTO protocols is becoming more difficult
resulting in extended timelines.
•  Aligning a “brand moniker” to a compound can protect the
corporate brand from adverse effects during clinical trials.
•  FDA Naming Guidance will become more complex, not less in the
future.
keyinsights
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
chimeric antigen receptor therapy
Factors Driving Early Stage Proprietary Naming
•  Drug companies are taking a page from the “high technology
playbook” when it comes to branding. The ‘First Mover Advantage’
is becoming more relevant as niche platforms define the importance
of being first to market. (i.e. CAR-T therapies)
•  “High Science” in the case of many emerging drug platforms is
becoming relevant as a communication messaging model. (Juno,
Bluebird Bio, Spark Therapeutics)
•  Trademarks are more difficult to secure. There will be less name
options available the longer one waits to secure the mark.
•  Many trademark professionals are mapping out a clear parallel filing
strategy for the PTO and FDA. (see slide)
keyinsights
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
@earlybranding=enhancedvaluation
Lentiglobin®
Lenti-D®
StarbeamStudy
NorthStarStudy
branded clinical studies
pipeline
product brands
Newly minted
public
companies are
branding early ;
not just the
product pipeline,
but also their
clinical studies.
Branding
enhances
valuation, leading
to
access to
financial
resources for
acquisitions
…and
partnerships
Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
evolutionary.
revolutionary.
disruptive.
24	
  Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
Brand Acumen
19 Leonard St.
NY, NY 10013
Bill Smith, CEO
(Call Bill. 704.906.3402)
william.smith@brandacumenstudios.com

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BIO Conference Upcoming Lecture" "The Case for Naming Sooner ...Than Later"

  • 1. The Case For Naming Sooner …Than Later April 15, 2015 Draft Presentation for BIO, 2015 Bill Smith, CEO Brand Acumen, LLC Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 2. chimeric antigen receptor therapy In March, 2015, a study of 79 pharmaceutical naming and trademark professionals was conducted by BrandAcumen. The purpose of the study was to define challenges and trends in the drug naming process. The key findings … The Research: Pharmaceutical Naming Impact Study Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 3. chimeric antigen receptor therapy Drug companies are developing trademarks for new products at an earlier stage of development in an effort to entrench a brand in the minds of HCPs, BioJournalists, Potential Patients,Affinity Proponents,Academia and the Financial Community. The Research: Pharmaceutical Naming Impact Study Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 4. chimeric antigen receptor therapy The overwhelming majority of the professionals surveyed in the study stated that they develop generic and trademark names, 91% and 87% respectively, before or during Phase II of clinical trials. The Research: Pharmaceutical Naming Impact Study Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 5. chimeric antigen receptor therapy The outcome of the study recommends seeking a trademark early — even during Phase I — as trademark searches have a low success rate. This fast movement is even more important for compounds with Expedited FDAReview Programs, Oncology, Orphan Drug, Cell and Gene Therapy Submissions. The Research: Pharmaceutical Naming Impact Study Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 6. chimeric antigen receptor therapy Moreover, the study suggests drug companies identify empty vessel names along with suggestive names, arguing that empty-vessel names can be easy to identify, protect and re-use. In addition, they pose less of a risk for rejection under medical error recognition evaluation or for conflicting with clinical trials results. The Research: Pharmaceutical Naming Impact Study Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 7. The Survey Overview Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 8. U.S.External TM Counsel (12) U.S. Internal (Company) TM Counsel (17) Chief Medical Officer (9) Regulatory (Internal) (14) Regulatory (Government) International (7) Commercialization/Launch Directors (20) Sample Profile Of Survey Respondents Total Respondents 79 Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 9. U.S.External TM Counsel (12) U.S. Internal (Company) TM Counsel (17) Chief Medical Officer (9) Regulatory (Internal) (14) Regulatory (Government) International (7) Commercialization/Launch Directors (20) Question: Compared to this time last year, do you feel compelled to begin the naming process earlier in the drug development cycle due to increased obstacles in clearing a name? 10 of 12 13 of 17 6 of 9 9 of 14 4 of 7 17 of 20 TheResearchResults: PharmaceuticalNamingImpactStudy The ‘Yes’ Responses Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 10. U.S.External TM Counsel (12) U.S. Internal (Company) TM Counsel (17) Chief Medical Officer (9) Regulatory (Internal) (14) Regulatory (Government) International (7) Commercialization/Launch Directors (20) Question: Do you believe that general costs associated with naming have escalated from two (2) years ago? 9 of 12 14 of 17 5 of 9 13 of 20 4 of 7 7 of 14 TheResearchResults: PharmaceuticalNamingImpactStudy The ‘Yes’ Responses Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 11. U.S.External TM Counsel (12) U.S. Internal (Company) TM Counsel (17) Chief Medical Officer (9) Regulatory (Internal) (14) Regulatory (Government) International (7) Commercialization/Launch Directors (20) Question: Do you believe that the growing number of FDA naming submissions has caused a slowdown in the review process over the past two (2) years? TheResearchResults: PharmaceuticalNamingImpactStudy The ‘Yes’ Responses 10 of 12 13 of 17 6 of 9 9 of 14 4 of 7 17 of 20 Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 12. The New Factors Impacting Naming BrandAcumen “The Global Leader in Pharmaceutical Name Development and Submissions” Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 13. chimeric antigen receptor therapy bioarbitrage In the BioArbitrage Fund, the business model acquires early stage assets (compounds), then quickly repackages and embellishes the asset for divestiture. By creating a brand name at Pre- Clinical/ Phase I development, the fund amplifies the ROI prior to ‘flipping the asset’ (divesting) to an acquirer. Identification of Asset (Pre-Clinical or Phase I) Negotiate Terms of Option Agreement with Seller Brand the Asset. Name, Design, Positioning, etc. . Create Offering Memorandum for Divestiture Market Asset to Potential Acquirers Close Transaction Triggering The Option Resulting in net ‘delta’ gain (arbitrage) BioArbitrage Process Early Stage Naming •  Pre-Clinical •  Phase I EmergingNewBusinessModelsareDrivingEarlyStage NameDevelopment thearbitrageimpact Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 14. chimeric antigen receptor therapy An orphan drug accelerator focused on developing and delivering life-transforming therapies for patients with severe and life- threatening rare diseases. Orphanetics is privately funded by public and private investors from the pharmaceutical, life sciences and global healthcare community. orphanetics Orphanetics engages in: •  Early Stage Naming of Clinical Programs •  Non-Proprietary Name Development •  Proprietary Name Development •  EPC Naming •  New Disease Branding •  MultiModal Orphan Drug Class •  Infinitive Phenoptics •  Vektür Micro Orphan Designation •  Harlequin Gan Syndrome •  Terracon SoSai Disorder EmergingNewBusinessModelsareDrivingEarlyStage NameDevelopment therarediseasebio-accelerator Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 15. @earlybranding=enhancedvaluation Lentiglobin® Lenti-D® StarbeamStudy NorthStarStudy branded clinical studies pipeline product brands Newly minted public companies are branding early ; not just the product pipeline, but also their clinical studies. Branding enhances valuation, leading to access to financial resources for acquisitions …and partnerships EmergingNewBusinessModelsareDrivingEarlyStage NameDevelopment Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 16. chimeric antigen receptor therapy EmergingNewBusinessModelsareDrivingEarlyStage ProprietaryNameDevelopment The dawn of ‘Name Repositories’ which own a broad portfolio of pharmaceutical and life science trademarks, service marks, platform identifiers, disease state nomenclature and domain names is the next wave indicator of the value of names as an intellectual property asset. These repositories operate as IP estates with a focus on capturing value in nomenclature as an asset. Emergence of Private Pharmaceutical Name Repositiories Structured around the concept of Microsoft Co-Founder Nathan Myhrvold’s Intellectual Ventures, this new breed of ‘name bank’ is creating a greater need to capture naming assets early. thenewbankers Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 17. chimeric antigen receptor therapy •  CAR-T •  GeneTherapy •  CRISPR Companies benefit from early stage naming as first to market leaders in their respective fields. Additionally, as these companies seek strategic partners and funding, brands become assets, which in turn enhance valuations. New Drug Technology Platforms SleepingBeauty RheoSwitch® ZIOPHARM platformbrands AttSite® UltraVector® LEAP® In the case of ZIOPHARM, brand recognition can also be key to securing pivotal strategic and financial partnerships. investment newplatform earlystagebrands EmergingNewBusinessModelsareDrivingEarlyStage ProprietaryNameDevelopment earlierstagenaming Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 18. EarlierNamingBehavior 18   As a result of a greater number of sponsors participating in the FDA’s Expedited Review Programs, the proliferation of name candidate submissions has created a strain on FDA resources for naming reviews. FDA’sExpeditedReviewPrograms Breakthrough Designation Accelerated Approval Fast Track Designation Priority Review The byproduct is that companies are beginning the naming process earlier to ensure approvals through the parallel channels of the FDA and PTO moreandmorenamesubmissions Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 19. chimeric antigen receptor therapy In the case of emerging drug discovery platforms, securing the first non-proprietary designation can also prove beneficial as competitors may be compelled to adopt variants of the nomenclature in their USAN filings. tisagenlecleucel-T tisa – gen – lec – leu – cel - T generic name non-proprietary name thenon-proprietaryadvantage EmergingNewBusinessModelsareDrivingEarlyStage Non-ProprietaryNameDevelopment AsWell Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 20. chimeric antigen receptor therapy TheResearchResults: PharmaceuticalNamingImpactStudy CAR-T anewlexicon Next generation technology platforms birth entire new lexicons overnight. With this, one must also consider the implications of the entire framework of the healthcare ecosystem when selecting name candidates. newlexicons:moreconfusion Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 21. chimeric antigen receptor therapy Factors Driving Early Stage Proprietary Naming •  In the case of rare diseases and high profile unmet needs (liver , pancreatic cancers, etc.), drug companies are recognizing the benefits of branding early to secure top of mind recognition sooner than later. •  Compliance with FDA and PTO protocols is becoming more difficult resulting in extended timelines. •  Aligning a “brand moniker” to a compound can protect the corporate brand from adverse effects during clinical trials. •  FDA Naming Guidance will become more complex, not less in the future. keyinsights Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 22. chimeric antigen receptor therapy Factors Driving Early Stage Proprietary Naming •  Drug companies are taking a page from the “high technology playbook” when it comes to branding. The ‘First Mover Advantage’ is becoming more relevant as niche platforms define the importance of being first to market. (i.e. CAR-T therapies) •  “High Science” in the case of many emerging drug platforms is becoming relevant as a communication messaging model. (Juno, Bluebird Bio, Spark Therapeutics) •  Trademarks are more difficult to secure. There will be less name options available the longer one waits to secure the mark. •  Many trademark professionals are mapping out a clear parallel filing strategy for the PTO and FDA. (see slide) keyinsights Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 23. @earlybranding=enhancedvaluation Lentiglobin® Lenti-D® StarbeamStudy NorthStarStudy branded clinical studies pipeline product brands Newly minted public companies are branding early ; not just the product pipeline, but also their clinical studies. Branding enhances valuation, leading to access to financial resources for acquisitions …and partnerships Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 24. evolutionary. revolutionary. disruptive. 24  Brand Acumen. “The Global Leader in Pharmaceutical Name Development and Submissions”
  • 25. Brand Acumen 19 Leonard St. NY, NY 10013 Bill Smith, CEO (Call Bill. 704.906.3402) william.smith@brandacumenstudios.com