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Introduction to
Discovery Partnerships
with Academia (DPAc)
Alternative Discovery & Development
GlaxoSmithKline R&D
A new model for partnering
with academia to discover
innovative medicines
DPAc model is unique
March 2015Introduction to DPAc
Collaborative Invention
Shared Ownership
Risk Embracing
Staged Pre-Clinical Research
Support
Development Milestones;
- Candidate Clinical NME(s)
- FTIH
- Clinical PoC
- Launch of medicine
Build integrated
partnerships that
can translate
innovative research
into medicines to
benefit patients
A collaborative approach from GSK
Giving academic researchers an opportunity to partner with GSK scientists, taking
advantage of our expertise and technical resources
What do we seek?
3
Clear
Therapeutic
Hypothesis
Coherent and
supportable
hypothesis that
modulating a target
will produce a
physiological effect
resulting in
therapeutic benefit
to particular
patients
March 2015Introduction to DPAc
Defined Target
Specific drug target
identified and some
understanding of type
of pharmacology
desired
(Exclusive)
Enabling
Expertise
Academic partner has
know-how and / or
expertise not (readily)
found elsewhere for
progressing the
target
Tractability
Path to identifying a
drug molecule can
be defined
Target knowledge
suggests that a
drug-like molecule
can be generated
Enabling GSK
Contribution
GSK has
capabilities and
expertise that will
help progress the
project
Key elements of DPAc
Focus on the medicine
• Collaborative partnerships focused on drug discovery
• Starts at any point from initiation of early screening, finishes with the medicine
Undertake the best science
• Minimal infrastructure: undertake projects independent of location or disease area
• Access to all GSK drug discovery and development capabilities
Share in the investment, share in the reward
• Both sides contribute – complementary match of skills where both academic institutions
and GSK can contribute to success
• Research funding synchronized with research goals
• Post-research milestone payments and royalties
• If partnership terminates, academic institution is free to progress
4March 2015Introduction to DPAc
Academic researchers who:
• Want to be involved in turning their
innovative research into medicines
• Contribute effort and resources to making
projects work
• Are recognized experts in their fields
• Bring unique capabilities to the collaboration
Who is best suited for DPAc?
5March 2015Introduction to DPAc
DPAc partnership
6March 2015Introduction to DPAc
• Co-authored and detailed work plan creates
framework to promote rapid project initiation
and execution
• Work together via Joint Research Committee
• Jointly invest time / energy / resources to
progress project at both partner sites
• Strong interactive relationships between
project teams
• Equitable approach to IP
- Academic institution receives commercial
rights if GSK terminates collaboration
Avalon/GSK
Newcos
Start a venture-
capitalist-backed
company, co-founded
with GSK
Pre-DPAc
Funds for promising
concepts that are too early
for full DPAc agreement
Discovery Fast
Track Challenge
Offers a chance to
win a screening
collaboration
with GSK
Multiple ways to collaborate with DPAc
March 2015Introduction to DPAc
Innovative medicines
to benefit patientsFull DPAc
YOU
and your
IDEAS
How DPAc projects operate
 Collaborative partnerships focus on drug discovery
 Start at any point from initiation of early screening to late lead optimization
 Consider any disease area
 Operate in any geography
 Seek complementary match of skills where both academic institution and GSK can
contribute to success
They are not
✗ Licensing or sponsored research agreements
✗ Support for exploratory work
✗ Focused on technology platforms
✗ Broad multi-project collaborations
✗ Open-ended funding streams
8XX March 2015An Introduction to DPAc
What capabilities can GSK bring
to DPAc partnerships?
9March 2015Introduction to DPAc
• Large-scale protein production
• HTS capacity 2 million compound set
• Medicinal chemistry and computational
molecular design
• Selectivity screening
• PK-PD modelling
• Flexible, high-tech assay platforms
Lead
Identification
Late Lead
Optimization
Early Lead
Optimization
Assay
Development
Target
Feasibility
• Biopharm discovery platforms
• Biopharm affinity maturation
• Encoded Library Technology*
>10 billion compounds
• Synthetic & analytical chemistry
• Preclinical development:
safety, chemistry, pharmacy
* Design, synthesis and selection of DNA-encoded small molecule
libraries. Clark et. al. Nature Chemical Biology 5, 647-654 (2009)
Candidate Selection
•
FTIH Start
•
Clinical POC
•
Launch
•
Lead
Identification
Late Lead
Optimization
Early Lead
Optimization
Assay
Development
Target
Feasibility
Partnerships focused on drug discovery
Planning all the way to the medicine
10March 2015Introduction to DPAc
Lead
Identification
Late Lead
Optimization
Early Lead
Optimization
Assay
Development
Target
Feasibility
Phase I Phase IIIPhase IIPre-Clinical
Early Drug
Discovery
Launch
&
Royalties
Drug Discovery Initiated
•
Screen Initiated
•
Lead Identified in vitro
•
Lead Identified in vitro
•
Typical GSK Activities
Typical Academic Activities
Shared activities between
academia and GSK
11March 2015Introduction to DPAc
Screening
Chemistry
Chemistry DMPK
Safety Pharmacy
Screening
Chemistry DMPK
Assay
Development
Assay Feasibility
Tool Generation
Physiological
Assays
Physiological
Assays in vivo
Models
Physiological
Assays in vitro
and in vivo
Assay
Development
Reagent
Generation
$
Value of
GSK Internal
Contribution
$
Value of
GSK Support
to Academic
Early Lead
Optimization
Late Lead
Optimization
Lead Identification
Tractability Assessment
and Assay Development
6 months 9-12 months9-12 months 9-12 months
Example activity plan
12
Assay
transfer
Physchem Pharmacy
Compound profiling (selectivity)
DMPK Toxicology
Compound profiling (biological and biochemical)
Medicinal chemistry Synthetic chemistry1˚ screen &
selectivity
ELT
Automation/
robustness
testing
Reagent production
1° Assay transfer
Reagent
generation
Assay
development
Compound profiling (phenotypic assessment)
Develop in vivo PD assays In vivo models PK/PD
MOA studies
Structural studies Clinical PD assay development
In vivo models efficacyDevelop cellular assay
NIH screen
Screen
initiated
Proof of
in vitro biology
Proof of
in vivo biology
Candidate
GSK
Academic
Partner
Dr Jonathan
Fallowfield
University of
Edinburgh
Mark
Bamford,
GSK
Seven active DPAc partnerships in Europe
13Introduction to DPAc
Treating Fibrotic
Liver Disease
Preventing
Multiple
Organ Failure in
Severe Acute
PancreatitisMr Damian
Mole,
University of
Edinburgh
John
Liddle,
GSK
Graft versus
Host Disease
(Biopharm)
Prof. Nathan
Karin, Rappaport
Institute, Israel
Jeremy
Griggs,
GSK
Treating a1-
Antitrypsin
Deficiency using
small molecule
stabilisersProf. David
Lomas,
University of
Cambridge
Andy
Pearce,
GSK
A disease
modifying
approach to the
treatment of
Huntington’s
Disease
Prof. Susann
Schweiger,
University of
Dundee
Iain
Uings,
GSK
Prof. Sir Mark
Pepys,
University College
London
Duncan
Holmes,
GSK
Stabilisers of
Transthyretin
as treatment for
Transthyretin
Amyloidosis
Topical Therapy
for Netherton
Syndrome,
Rosacea and
Atopic DermatitisProf. Alain
Hovnanian,
Paris
Descartes
University
John
Liddle,
GSK
March 2015
Five active DPAc partnerships in North America
14Introduction to DPAc March 2015
Z
Treatment of
Cystic Fibrosis
Prof. Christine
Bear
SickKids Hospital
Toronto
Jakob
Busch-
Petersen,
GSK
Treatment of
Alzheimer’s
Disease
Prof. Paul
Lombroso
Yale
University
Dennis
Yamashita,
GSK
Prof. Roger
Cone
Vanderbilt
University
David
Becherer,
GSK
Treatment of
Obesity
Treatment of
Triplet Repeat
Diseases
Prof. Christopher
Pearson
SickKids Hospital
Toronto
Debra
Peattie,
GSK
Prof. Nicholas
Tonks
Cold Spring
Harbor Labs
Jon Collins,
GSK
Treatment of
Obesity
and Type 2
Diabetes
Discovery Fast Track Challenge
• Innovative approach to sourcing new
partnership ideas – inviting academic
researchers to propose project ideas in a
challenge-like format
• Rigorous review and detailed face-to-face
feedback and advice to investigators
selected as finalists; up to 30 finalists will be
selected in 2015
• Partnership with challenge winners (up to
12 in 2015) to perform high-throughput and
encoded library screening of their target
• Promising results may lead to an
opportunity for the academic institution and
GSK to collaborate via a full DPAc
partnership or via supplied chemical probes
15March 2015Introduction to DPAc
For Discovery Fast Track Challenge winners
• GSK will provide state-of-the-art capabilities
• Devise optimal screening strategy (e.g. HTS, Encoded Library
Technologies)
• Adapt and scale biological reagents for screening
• Miniaturize assays for HTS (~2M cpds)
• Run screens, analyze output and "qualify" hits
• Principal Investigator (PI) joins team of GSK scientists to execute the screen
and follow up hits – often culminating in tests within PI's lab (e.g., complex
cellular assays)
• GSK may provide up to 3 chemical structures of selected chemical probe(s) to
help further PI’s research and potentially lead to high-impact publications,
subject to GSK’s existing internal and external obligations
• Promising results may lead to a full DPAc collaboration with GSK to create a
novel medicine with the DPAc team
16March 2015Introduction to DPAc
2014 North American Discovery Fast Track
Challenge results
17March 2015Introduction to DPAc
196
Proposals Submitted
from
105
Participating Institutions
12
Finalists
6
Winners
40%
Increase in
proposals
submitted
from 2013
2014 European Discovery Fast Track
Challenge results
18March 2015Introduction to DPAc
232
Proposals Submitted
from
131
Institutions
14
Finalists
9
Winners
24
Countries
DPAc and Discovery Fast Track Challenge
collaborations
19March 2015Introduction to DPAc
Discovery Fast Track
Challenge 2013
Winner Institutions
• Pennsylvania State University
• Albert Einstein College of Medicine of
Yeshiva University
• Boston University and University of
California, San Francisco
• Harvard Medical School
• University of Pennsylvania
• Université de Sherbrooke
• University of North Carolina at
Chapel Hill (x2)
Discovery Fast Track
Challenge 2014
Winner Institutions
• Mayo Clinic
• Johns Hopkins
• University of Pennsylvania
• University of Texas Southwestern
Medical Center
• University of Iowa
• University of Toronto
• University of Milan
• University of Cambridge (x3)
• National Institute of Health and Medical
Research
• Research Center for Molecular Medicine
• King’s College London
• VU University Medical
DPAc Partnership
Institutions
• University of Edinburgh
• University of Dundee
• University of Nottingham
• University of Cambridge
• University College, London
• Université Paris Descartes
• University of Dundee (University of
Mainz)
• Rappaport Family Institute, Haifa,
Israel
• Fred Hutchinson Cancer Research
Center
• Vanderbilt University
• University of Toronto/Hospital for Sick
Kids
• Yale University
Discovery Fast Track Challenge proposals
yield broad therapeutic coverage
20March 2015Introduction to DPAc
Europe 2014 (232 total)North America 2014 (196 total)
Discovery Fast Track Challenge 2015
21March 2015Introduction to DPAc
Challenge
Opened
Mar 23
Europe
North America
Registration
Closes
Apr 24
Europe
North America
TTO Approval
Deadline
May 8
Europe
North America
Finalist
Presentations
Jul 14-17
Europe
(Stevenage, UK)
Sept 28-30
North America
(PA, US)
Winners
announced
Jan 2016
Europe
North America
Investigator submits
1 page non-
confidential proposal
TTO approval required
for GSK review
GSK selects finalists,
assigns mentors
Expanded confidential
proposals
Material transfer and
work-plan agreement s
signed
GSK scientist teams
assigned to project,
and work begins
towards screening
1 2 3 4 5
Find more information at gsk.com/discoveryfasttrack
Who we are: dpac.gsk.com
22March 2015Introduction to DPAc
Duncan Holmes
European Head
LONDON
Mark Bamford
Chemistry,
LONDON
Iain Uings
Biology, LONDON
& CALIFORNIA
John Liddle
Chemistry,
LONDON
Ann Walker
Chemistry,
LONDON
Stephane Huet
Biology,
PARIS
Jeremy Griggs
Biology,
LONDON
Danuta Mossakowska
Biology,
LONDON
Andy Pearce
Biology,
LONDON
Colin Macphee
Biology,
PHL
Jakob Busch-Petersen
Chemistry,
PHL
Andy Pope
Biology,
PHL
Carolyn Buser-
Doepner
Global Head, PHL
Dan Paone
Chemistry,
PHL
Dedicated team of scientists, each of
whom has proven track record in drug
discovery
Your gateway to GSK’s global
expertise and resources
Jon Collins
Chemistry,
RTP, NC
Katherine Widdowson
Chemistry,
CALIFORNIA
Debra Peattie
Biology,
BOSTON
Dave Parry
Biology,
CALIFORNIA
Mike Bishop
Chemistry,
RTP, NC
Dave Becherer
Biochem ,
RTP, NC
Dennis Yamashita
Chemistry,
BOSTON

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Discover innovative medicines through academic partnerships

  • 1. Introduction to Discovery Partnerships with Academia (DPAc) Alternative Discovery & Development GlaxoSmithKline R&D A new model for partnering with academia to discover innovative medicines
  • 2. DPAc model is unique March 2015Introduction to DPAc Collaborative Invention Shared Ownership Risk Embracing Staged Pre-Clinical Research Support Development Milestones; - Candidate Clinical NME(s) - FTIH - Clinical PoC - Launch of medicine Build integrated partnerships that can translate innovative research into medicines to benefit patients A collaborative approach from GSK Giving academic researchers an opportunity to partner with GSK scientists, taking advantage of our expertise and technical resources
  • 3. What do we seek? 3 Clear Therapeutic Hypothesis Coherent and supportable hypothesis that modulating a target will produce a physiological effect resulting in therapeutic benefit to particular patients March 2015Introduction to DPAc Defined Target Specific drug target identified and some understanding of type of pharmacology desired (Exclusive) Enabling Expertise Academic partner has know-how and / or expertise not (readily) found elsewhere for progressing the target Tractability Path to identifying a drug molecule can be defined Target knowledge suggests that a drug-like molecule can be generated Enabling GSK Contribution GSK has capabilities and expertise that will help progress the project
  • 4. Key elements of DPAc Focus on the medicine • Collaborative partnerships focused on drug discovery • Starts at any point from initiation of early screening, finishes with the medicine Undertake the best science • Minimal infrastructure: undertake projects independent of location or disease area • Access to all GSK drug discovery and development capabilities Share in the investment, share in the reward • Both sides contribute – complementary match of skills where both academic institutions and GSK can contribute to success • Research funding synchronized with research goals • Post-research milestone payments and royalties • If partnership terminates, academic institution is free to progress 4March 2015Introduction to DPAc
  • 5. Academic researchers who: • Want to be involved in turning their innovative research into medicines • Contribute effort and resources to making projects work • Are recognized experts in their fields • Bring unique capabilities to the collaboration Who is best suited for DPAc? 5March 2015Introduction to DPAc
  • 6. DPAc partnership 6March 2015Introduction to DPAc • Co-authored and detailed work plan creates framework to promote rapid project initiation and execution • Work together via Joint Research Committee • Jointly invest time / energy / resources to progress project at both partner sites • Strong interactive relationships between project teams • Equitable approach to IP - Academic institution receives commercial rights if GSK terminates collaboration
  • 7. Avalon/GSK Newcos Start a venture- capitalist-backed company, co-founded with GSK Pre-DPAc Funds for promising concepts that are too early for full DPAc agreement Discovery Fast Track Challenge Offers a chance to win a screening collaboration with GSK Multiple ways to collaborate with DPAc March 2015Introduction to DPAc Innovative medicines to benefit patientsFull DPAc YOU and your IDEAS
  • 8. How DPAc projects operate  Collaborative partnerships focus on drug discovery  Start at any point from initiation of early screening to late lead optimization  Consider any disease area  Operate in any geography  Seek complementary match of skills where both academic institution and GSK can contribute to success They are not ✗ Licensing or sponsored research agreements ✗ Support for exploratory work ✗ Focused on technology platforms ✗ Broad multi-project collaborations ✗ Open-ended funding streams 8XX March 2015An Introduction to DPAc
  • 9. What capabilities can GSK bring to DPAc partnerships? 9March 2015Introduction to DPAc • Large-scale protein production • HTS capacity 2 million compound set • Medicinal chemistry and computational molecular design • Selectivity screening • PK-PD modelling • Flexible, high-tech assay platforms Lead Identification Late Lead Optimization Early Lead Optimization Assay Development Target Feasibility • Biopharm discovery platforms • Biopharm affinity maturation • Encoded Library Technology* >10 billion compounds • Synthetic & analytical chemistry • Preclinical development: safety, chemistry, pharmacy * Design, synthesis and selection of DNA-encoded small molecule libraries. Clark et. al. Nature Chemical Biology 5, 647-654 (2009)
  • 10. Candidate Selection • FTIH Start • Clinical POC • Launch • Lead Identification Late Lead Optimization Early Lead Optimization Assay Development Target Feasibility Partnerships focused on drug discovery Planning all the way to the medicine 10March 2015Introduction to DPAc Lead Identification Late Lead Optimization Early Lead Optimization Assay Development Target Feasibility Phase I Phase IIIPhase IIPre-Clinical Early Drug Discovery Launch & Royalties Drug Discovery Initiated • Screen Initiated • Lead Identified in vitro • Lead Identified in vitro •
  • 11. Typical GSK Activities Typical Academic Activities Shared activities between academia and GSK 11March 2015Introduction to DPAc Screening Chemistry Chemistry DMPK Safety Pharmacy Screening Chemistry DMPK Assay Development Assay Feasibility Tool Generation Physiological Assays Physiological Assays in vivo Models Physiological Assays in vitro and in vivo Assay Development Reagent Generation $ Value of GSK Internal Contribution $ Value of GSK Support to Academic
  • 12. Early Lead Optimization Late Lead Optimization Lead Identification Tractability Assessment and Assay Development 6 months 9-12 months9-12 months 9-12 months Example activity plan 12 Assay transfer Physchem Pharmacy Compound profiling (selectivity) DMPK Toxicology Compound profiling (biological and biochemical) Medicinal chemistry Synthetic chemistry1˚ screen & selectivity ELT Automation/ robustness testing Reagent production 1° Assay transfer Reagent generation Assay development Compound profiling (phenotypic assessment) Develop in vivo PD assays In vivo models PK/PD MOA studies Structural studies Clinical PD assay development In vivo models efficacyDevelop cellular assay NIH screen Screen initiated Proof of in vitro biology Proof of in vivo biology Candidate GSK Academic Partner
  • 13. Dr Jonathan Fallowfield University of Edinburgh Mark Bamford, GSK Seven active DPAc partnerships in Europe 13Introduction to DPAc Treating Fibrotic Liver Disease Preventing Multiple Organ Failure in Severe Acute PancreatitisMr Damian Mole, University of Edinburgh John Liddle, GSK Graft versus Host Disease (Biopharm) Prof. Nathan Karin, Rappaport Institute, Israel Jeremy Griggs, GSK Treating a1- Antitrypsin Deficiency using small molecule stabilisersProf. David Lomas, University of Cambridge Andy Pearce, GSK A disease modifying approach to the treatment of Huntington’s Disease Prof. Susann Schweiger, University of Dundee Iain Uings, GSK Prof. Sir Mark Pepys, University College London Duncan Holmes, GSK Stabilisers of Transthyretin as treatment for Transthyretin Amyloidosis Topical Therapy for Netherton Syndrome, Rosacea and Atopic DermatitisProf. Alain Hovnanian, Paris Descartes University John Liddle, GSK March 2015
  • 14. Five active DPAc partnerships in North America 14Introduction to DPAc March 2015 Z Treatment of Cystic Fibrosis Prof. Christine Bear SickKids Hospital Toronto Jakob Busch- Petersen, GSK Treatment of Alzheimer’s Disease Prof. Paul Lombroso Yale University Dennis Yamashita, GSK Prof. Roger Cone Vanderbilt University David Becherer, GSK Treatment of Obesity Treatment of Triplet Repeat Diseases Prof. Christopher Pearson SickKids Hospital Toronto Debra Peattie, GSK Prof. Nicholas Tonks Cold Spring Harbor Labs Jon Collins, GSK Treatment of Obesity and Type 2 Diabetes
  • 15. Discovery Fast Track Challenge • Innovative approach to sourcing new partnership ideas – inviting academic researchers to propose project ideas in a challenge-like format • Rigorous review and detailed face-to-face feedback and advice to investigators selected as finalists; up to 30 finalists will be selected in 2015 • Partnership with challenge winners (up to 12 in 2015) to perform high-throughput and encoded library screening of their target • Promising results may lead to an opportunity for the academic institution and GSK to collaborate via a full DPAc partnership or via supplied chemical probes 15March 2015Introduction to DPAc
  • 16. For Discovery Fast Track Challenge winners • GSK will provide state-of-the-art capabilities • Devise optimal screening strategy (e.g. HTS, Encoded Library Technologies) • Adapt and scale biological reagents for screening • Miniaturize assays for HTS (~2M cpds) • Run screens, analyze output and "qualify" hits • Principal Investigator (PI) joins team of GSK scientists to execute the screen and follow up hits – often culminating in tests within PI's lab (e.g., complex cellular assays) • GSK may provide up to 3 chemical structures of selected chemical probe(s) to help further PI’s research and potentially lead to high-impact publications, subject to GSK’s existing internal and external obligations • Promising results may lead to a full DPAc collaboration with GSK to create a novel medicine with the DPAc team 16March 2015Introduction to DPAc
  • 17. 2014 North American Discovery Fast Track Challenge results 17March 2015Introduction to DPAc 196 Proposals Submitted from 105 Participating Institutions 12 Finalists 6 Winners 40% Increase in proposals submitted from 2013
  • 18. 2014 European Discovery Fast Track Challenge results 18March 2015Introduction to DPAc 232 Proposals Submitted from 131 Institutions 14 Finalists 9 Winners 24 Countries
  • 19. DPAc and Discovery Fast Track Challenge collaborations 19March 2015Introduction to DPAc Discovery Fast Track Challenge 2013 Winner Institutions • Pennsylvania State University • Albert Einstein College of Medicine of Yeshiva University • Boston University and University of California, San Francisco • Harvard Medical School • University of Pennsylvania • Université de Sherbrooke • University of North Carolina at Chapel Hill (x2) Discovery Fast Track Challenge 2014 Winner Institutions • Mayo Clinic • Johns Hopkins • University of Pennsylvania • University of Texas Southwestern Medical Center • University of Iowa • University of Toronto • University of Milan • University of Cambridge (x3) • National Institute of Health and Medical Research • Research Center for Molecular Medicine • King’s College London • VU University Medical DPAc Partnership Institutions • University of Edinburgh • University of Dundee • University of Nottingham • University of Cambridge • University College, London • Université Paris Descartes • University of Dundee (University of Mainz) • Rappaport Family Institute, Haifa, Israel • Fred Hutchinson Cancer Research Center • Vanderbilt University • University of Toronto/Hospital for Sick Kids • Yale University
  • 20. Discovery Fast Track Challenge proposals yield broad therapeutic coverage 20March 2015Introduction to DPAc Europe 2014 (232 total)North America 2014 (196 total)
  • 21. Discovery Fast Track Challenge 2015 21March 2015Introduction to DPAc Challenge Opened Mar 23 Europe North America Registration Closes Apr 24 Europe North America TTO Approval Deadline May 8 Europe North America Finalist Presentations Jul 14-17 Europe (Stevenage, UK) Sept 28-30 North America (PA, US) Winners announced Jan 2016 Europe North America Investigator submits 1 page non- confidential proposal TTO approval required for GSK review GSK selects finalists, assigns mentors Expanded confidential proposals Material transfer and work-plan agreement s signed GSK scientist teams assigned to project, and work begins towards screening 1 2 3 4 5 Find more information at gsk.com/discoveryfasttrack
  • 22. Who we are: dpac.gsk.com 22March 2015Introduction to DPAc Duncan Holmes European Head LONDON Mark Bamford Chemistry, LONDON Iain Uings Biology, LONDON & CALIFORNIA John Liddle Chemistry, LONDON Ann Walker Chemistry, LONDON Stephane Huet Biology, PARIS Jeremy Griggs Biology, LONDON Danuta Mossakowska Biology, LONDON Andy Pearce Biology, LONDON Colin Macphee Biology, PHL Jakob Busch-Petersen Chemistry, PHL Andy Pope Biology, PHL Carolyn Buser- Doepner Global Head, PHL Dan Paone Chemistry, PHL Dedicated team of scientists, each of whom has proven track record in drug discovery Your gateway to GSK’s global expertise and resources Jon Collins Chemistry, RTP, NC Katherine Widdowson Chemistry, CALIFORNIA Debra Peattie Biology, BOSTON Dave Parry Biology, CALIFORNIA Mike Bishop Chemistry, RTP, NC Dave Becherer Biochem , RTP, NC Dennis Yamashita Chemistry, BOSTON