implementing the sps… one year later karolina maciag (harvard medical mit) jillian irwin (harvard...
TRANSCRIPT
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Implementing
the SPS…
One Year LaterKarolina Maciag (Harvard Medical
MIT)
Jillian Irwin (Harvard College)
UAEM International Conference
October 9, 2010
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What does this document say?
How will TTOs implement the Principles?
What does this document mean for UAEM?
How did we get here?
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The SPS is Born
Yale
Provost
agrees to
articulate
policies
Discuss Stakeholder Meeting,
Committee on Global Access
Licensing with Dean of Public
Health
Crimson
op-ed
exchange
Faculty outreach for Working
Group on Licensing
First meeting
with OTD,
friendly
Yale
monthly
OTD
meetings
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GSK shaming Harvard
response
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The SPS is Born
Yale
Provost
agrees to
articulate
policies
Discuss Stakeholder Meeting,
Committee on Global Access
Licensing with Dean of Public
Health
Crimson
op-ed
exchange
Faculty outreach for Working
Group on Licensing
First meeting
with OTD,
friendly
Petition to
Provost
Yale
monthly
OTD
meetings
Provost and
TTO Head
reveal plans
to develop
multi-
university
agreement
Meeting
with OTD
and
CEOs,
unfriendly
Multi-
University
Roundtable
Say Yes
To Drugs
Campaign
SPS
Launched
Meeting
with
Harvard
President
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SPS
Launched
Say Yes
To Drugs
Rally
OTD-
UAEM
6-month
meeting
16 additional institutions
sign on to the SPS
OTD
Participates
at UAEM-
Brazil
meeting
OTD -
UAEM
biannual
meeting
CONFERENCE!
The SPS in its first year
UAEM
publishes
response to
SPS
OTD
patent
pool
chat
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Current Signatories
Institution Signing DateAssociation of University Technology Managers 11/9/2009Boston Univ 11/9/2009Brown Univ 11/9/2009Harvard Univ 11/9/2009Univ of Pennsylvania 11/9/2009Yale Univ 11/9/2009Oregon Health & Science University 11/9/2009National Institutes of Health 11/10/2009University of Illinois Chicago 11/10/2009University of Illinois Urbana-Champaign 11/11/2009Centers for Disease Control and Prevention 11/12/2009University of Vermont and State Agricultural College 11/19/2009Duke University and Duke Medicine 12/1/2009University of British Columbia 1/10/2010Bilkent University 1/27/2010El Colegio de México 1/27/2010New York University 2/4/2010Tecnologico de Monterrey 2/13/2010Jawaharlal Nehru University 2/18/2010Najit Technologies, Inc. 3/4/2010Brigham & Women's Hospital 3/15/2010Florida State University 3/29/2010Massachusetts General Hospital 3/29/2010
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SPS
Launched
Say Yes
To Drugs
Rally
OTD-
UAEM
6-month
meeting
16 additional institutions
sign on to the SPS
OTD
Participates
at UAEM-
Brazil
meeting
OTD -
UAEM
biannual
meeting
CONFERENCE!
Implementation
Transparency
?UAEM
publishes
response to
SPS
OTD
patent
pool
chat
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NIH implementation: HIV drug in patent pool
Harvard: 3 licenses so far
Other successes?
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UAEM Framework:
Access to medicines and health-related technologies for all is
the primary purpose of technology transfer of health-related
innovations.
Rhetoric
SPS
- We have created new methods to deploy cutting-edge
knowledge toward potential public benefit
- Licensing practices involved in such commercialization have
expanded to promote explicitly global access to university-
developed technologies, ensuring that advances in health
reach those who need them most.
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UAEM Framework:
Technology transfer should protect access to the final end
product needed by patients (e.g., formulated pills or vaccines).
Access to end products
SPS
It is not always possible at the time of license negotiation to
anticipate all of the ways a health-related technology may be
used in developing countries. Accordingly, we will strive to
preserve our institutions’ future rights to negotiate effective
global access terms through implementation of such measures
as notice requirements coupled with “agreements to agree.”
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UAEM Framework:
Generic provision is the best way to ensure access in resource-limited
countries for products that also have markets in developed countries. Legal
barriers to generic production of these products for use in resource-limited
countries should therefore be removed.
Generic provision
SPS
In cases where universities can fully preclude intellectual property barriers
to generic provision by not patenting in developing countries, or by filing
and abandoning patents, we will pursue these strategies.
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Generic provision, cont.: Exceptions
SPS
…it may be necessary to account for special circumstances (e.g., in India,
China or Brazil) that may warrant patenting in such countries on a case-by-
case basis, including but not limited to:
The existence in a developing country of pharmaceutical
manufacturing capacity suitable to support product distribution both
within and outside the developing world; or
The opportunity to gain greater leverage in seeking concessions, such as
access to others’ intellectual property, that would help to ensure that the
health-related technology can be made available affordably; or
To enable our licensee(s) to implement tiered pricing in those developing
countries where a significant private market exists.
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Alternatives to generic provision
SPS
In those cases where we pursue patent rights, we will negotiate license agreements that
draw upon a variety of strategies that seek to align incentives… to promote broad
access … not limited to:
• Financial incentives to licensees (e.g., elimination or adjustments to royalty rates);
• Reserved or ‘march-in’ rights, mandatory sublicenses or non-assert provisions;
• Affirmative obligations of diligence, with license reduction, conversion (i.e., to non-
exclusivity) or termination as the penalty for default; and
• Tiered- or other appropriate pricing on a humanitarian basis (e.g., subsidized, at-cost
or no-cost).
UAEM Framework:
where generic provision is forecast to be technically or economically infeasible, “at-
cost” or other provisioning requirements should be used as a supplement to generic
provisioning terms but should never replace those terms.
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UAEM Framework:
Proactive licensing provisions are essential to ensure that follow-on patents
and data exclusivity cannot be used to block generic production. Other
barriers may need to be addressed for the licensing of biologics.
Proactive licensing
SPS
Early publication and wide dissemination of results will be encouraged to
reduce opportunities for interfering patents.
…
In those cases where we pursue patent rights, we will negotiate license
agreements that draw upon a variety of strategies [including]…
Reserved or ‘march-in’ rights, mandatory sublicenses or non-assert provisions
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UAEM Framework:
University licensing should be systematic in its approach, sufficiently
transparent to verify its effectiveness, and based on explicit metrics that
measure the success of technology transfer by its impact on access and
continued innovation.
Metrics
SPS:
We will work together to develop and apply meaningful metrics to evaluate
the success of our efforts to facilitate global access and support continued
innovation with particular relevance to global health.
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Work for us: Living document
SPS
Educate others and encourage their consideration,
endorsement and application of the principles articulated in this
statement; and
[Get your university to sign on?]
Revisit these principles on a biennial basis, to ensure that they
reflect currently-understood best practices.
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• What will the SPS mean?
• GOVERNANCE: What type of mechanism does UAEM
need to push for so that GALF principles are implemented
at SPS schools?-Institutional review boards including expert faculty,
research faculty, students, administrators- Other?
• TRANSPARENCY: How can UAEM keep apprised of
licensing deals and promote collaboration among TTOs?- issue of agreement confidentiality- biannual meeting - online database of deals - Other?
Concretization of the SPS
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Work for us: Vigilance on Implementation
SPS
1 The decision about precisely which health-related
technologies merit global access licensing is complicated and
will be the subject of ongoing evaluation by our organizations.
While the principles articulated in this statement currently are
directed primarily at therapeutics and vaccines, their
application to medical diagnostics and devices will be
assessed case-by-case on an ongoing basis
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UAEM Framework:
Every university-developed technology with potential for further
development into a drug, vaccine, or medical diagnostic should be licensed
with a concrete and transparent strategy
Work for us: Transparency
SPS
[We commit to] Share with one another our collective experiences from
working with our licensees in implementing these principles to continually
advance our goals. To that end, we will cooperate in the creation of:
A compendium of best practices, tools and techniques; and
A consistent means of reporting on our global access initiatives and
activities.
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SPS vs. Something Stronger
• Should UAEM at non-signatory institutions demand SPS + concessions…
• or a document (and practices) that are more GALF-like?
• Risk of falling short:
GSK patent
pool:
50 LDCs
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Risk of falling short without the SPS
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Pushing for SPS Adoption
Pros- Institutions more likely
to sign on- Might lead to other GAL-
like agreement- If endorsed, will
participate in consortium, revisions, best-practices/collaborative activities
ConsSPS Shortcomings!
-GH application-BRIC-Generic prioritization-Access to end product-Transparency/ Accountability(Complacency)
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How do we push for SPS Adoption?
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Say Yes To Drugs
• Harvard Campaign of Fall 2009 that led to SPS drafting and adoption
• T-shirts, Viral video, petition, benefit dance, op-eds, BRIC-or-Treat, Rally
• Main Challenge: Storytelling • Solution: Provocative T-Shirts!
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Meeting with Harvard’s PresidentJust prior to SPS (October 2009)
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The BRIC Wall
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Storytelling
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SPS Advocacy
• How has SPS advocacy been going at your universities?– Successes?
• How did you accomplish it? What made your action effective?
– Obstacles?• Strategies to overcome them?• How can UAEM schools support each other?