Search Results For:
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Agreement title
Effective date
Partner type
Technology
Development stage
European Commission - CureVac, COVID-19 Vaccine Advance Purchase Agreement
2020
Government
Industry
Industry
Vaccine
Late clinical (Phase 3)
Commercialization
Commercialization
Alnylam Pharmaceuticals - University of British Columbia- AlCana Technology, Sponsored Research Agreement
2009
Academic institution
Industry
Industry
Drug
Vaccine
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
PATH - Aridis, Rotavirus Vaccine Development Agreement
2007
Industry
Product development partnership
Product development partnership
Vaccine
Early clinical (through Phase 2)
AUTM Model Inter-Institutional Research Collaboration Agreement
2015
Academic institution
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
AUTM Preliminary Patent Management Agreement
2013
Academic institution
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Yale University - BIND Biosciences, Cancer Therapeutic, Exclusive License Agreement
2013
Academic institution
Industry
Industry
Drug
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Biological E - Dynavax Technologies, COVID-19 Vaccine Adjuvant Supply Agreement
2021
Industry
Vaccine
Late clinical (Phase 3)
Commercialization
Commercialization
Gates Foundation - Arsanis, S. Aureus Antibody Strategic Relationship Letter Agreement
2017
Funder
Industry
Industry
Drug
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Gates Foundation - CureVac, Global Access Commitments Agreement
2015
Funder
Industry
Industry
Drug
Vaccine
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Late clinical (Phase 3)
Commercialization
Field Testing
Gates Foundation - Icosavax, COVID-19 Vaccine Global Access and Price Commitments Agreement
2021
Funder
Industry
Industry
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
Boston University Startup Exclusive License Template
2012
Academic institution
Industry
Non-profit research organization
Product development partnership
Industry
Non-profit research organization
Product development partnership
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
CEPI - CureVac, Framework Partnering Agreement
2019
Funder
Industry
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
- Equitable access | Ensuring continuity
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Clinical trial conduct
- Business model | Regulatory strategy
- Protecting & sharing information | Information sharing
- Protecting & sharing information | Technology transfer
- Intellectual property | License grants
- Liability | Representations & warranties
- Term & termination | Effects of termination
CEPI - University of Oxford - Barinthus Biotherapeutics, ChAdOx1 MERS Vaccine R&D Funding Agreement
2023
Academic institution
Funder
Industry
Funder
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
CSIC - MPP (C-TAP), COVID-19 Diagnostic, Patent & Material License Agreement
2021
Government
Multilateral organization
Multilateral organization
Diagnostic
Commercialization
CureVac - GSK, COVID-19 Vaccine Collaboration and License Agreement
2021
Industry
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
DNDi Template Development Collaboration and License Agreement
2023
Academic institution
Industry
Non-profit research organization
Product development partnership
Industry
Non-profit research organization
Product development partnership
Drug
Early clinical (through Phase 2)
Late clinical (Phase 3)
Late clinical (Phase 3)
- Equitable access | Ensuring continuity
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Product supply
- Term & termination | Termination & withdrawal
DNDi Template Research Collaboration and License Agreement
2023
Academic institution
Industry
Non-profit research organization
Product development partnership
Industry
Non-profit research organization
Product development partnership
Drug
Discovery/Concept
Preclinical
Preclinical
DNDi - BioDelivery Sciences International, Visceral Leishmaniasis Research Collaboration Agreement
2009
Industry
Product development partnership
Product development partnership
Drug
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
DNDi/GARDP - Entasis, Gonorrhoea Medication, Collaboration Agreement
2017
Industry
Product development partnership
Product development partnership
Drug
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
Funder Development Partnering Agreement Template
2018
Funder
Industry
Non-profit research organization
Product development partnership
Industry
Non-profit research organization
Product development partnership
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
- Equitable access | Ensuring continuity
- Equitable access | Access plans & principles
- Equitable access | Preparedness & response
- Equitable access | Affordable pricing
- Equitable access | Territory access commitments
- Business model | Clinical trial conduct
- Business model | Quality management
- Business model | Regulatory strategy
- Business model | Governance
- Business model | Payment structures
- Intellectual property | License grants
- Liability | Indemnification & liability
- Term & termination | Effects of termination
Gates Foundation - BioNTech, TB & HIV Product Strategic Letter Agreement
2019
Funder
Industry
Industry
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Gates Foundation - Visterra, Strategic Relationship Letter Agreement
2012
Funder
Industry
Industry
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Israel - Pfizer, Epidemiological Evidence Collaboration Agreement
2021
Government
Industry
Industry
Vaccine
Late clinical (Phase 3)
Commercialization
Field Testing
Commercialization
Field Testing
UK Lambert Toolkit, Model Consortium Agreement D
2018
Academic institution
Industry
Industry
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
MPP – Afrigen Biologics, COVID-19 mRNA-Based Vaccines and Therapeutics, Grant Agreement
2022
Industry
Multilateral organization
Multilateral organization
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
MPP - Biovac, mRNA Vaccine Technology Transfer Agreement
2024
Industry
Multilateral organization
Multilateral organization
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
BMS - MPP, Hepatitis C Antiviral (daclatasvir - DAC) License & Tech Transfer Agreement
2016
Industry
Multilateral organization
Multilateral organization
Drug
Commercialization
Gilead - MPP - Arene Lifesciences, HIV Therapeutic License Agreement
2018
Industry
Multilateral organization
Multilateral organization
Drug
Commercialization
Pfizer - MPP, TB Therapeutic (Sutezolid) Non-Exclusive License Agreement
2019
Industry
Multilateral organization
Multilateral organization
Drug
Commercialization
MPP – South African Medical Research Council, COVID-19 mRNA-Based Vaccines and Therapeutics, Grant Agreement
2022
Government
Multilateral organization
Multilateral organization
Drug
Vaccine
Vaccine
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
NIAID - AbCellera, COVID-19 Exclusive Patent License Agreement
2020
Government
Industry
Industry
Vaccine
Commercialization
NIH - GeoVax, Non-Exclusive Patent and Biological Materials License Agreement
2020
Government
Industry
Industry
Vaccine
Preclinical
Commercialization
Commercialization
NIH – MPP (C-TAP), COVID-19 Technologies, Patent and Biological Material License Agreement
2022
Government
Multilateral organization
Multilateral organization
Diagnostic
Drug
Vaccine
Drug
Vaccine
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
Ocugen-BBIL, COVID-19 Vaccine (Covaxin), Co-development, Supply & Commercialization Agreement
2021
Industry
Vaccine
Late clinical (Phase 3)
Commercialization
Commercialization
Academic Institution - Company, Research Collaboration Agreement
2016
Academic institution
Industry
Industry
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
US Department of Defense – Regeneron, COVID-19 Antibodies Large-Scale Manufacturing Agreement
2020
Government
Industry
Industry
Drug
Late clinical (Phase 3)
Commercialization
Commercialization
UK Lambert Toolkit, Model Consortium Agreement A
2018
Academic institution
Industry
Industry
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
UK Lambert Toolkit, Model Consortium Agreement B
2018
Academic institution
Industry
Industry
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
UK Lambert Toolkit, Model Consortium Agreement C
2018
Academic institution
Industry
Industry
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
University of Chile - MPP (C-TAP), COVID-19 Diagnostic Material & Know-How License Agreement
2023
Academic institution
Multilateral organization
Multilateral organization
Diagnostic
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Late clinical (Phase 3)
Commercialization
University of Washington - MPP, Long-acting Injectable HIV Treatment License Agreement
2021
Academic institution
Multilateral organization
Multilateral organization
Drug
Preclinical
Wellcome Trust - Alto Neuroscience, Bipolar Depression Therapeutic Convertible Loan Agreement
2024
Funder
Industry
Industry
Drug
Early clinical (through Phase 2)
Late clinical (Phase 3)
Late clinical (Phase 3)
WHO Template Material Transfer Agreement
2015
Academic institution
Industry
Multilateral organization
Non-profit research organization
Product development partnership
Industry
Multilateral organization
Non-profit research organization
Product development partnership
Device
Diagnostic
Drug
Vaccine
Diagnostic
Drug
Vaccine
Discovery/Concept
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
Preclinical
Early clinical (through Phase 2)
Late clinical (Phase 3)
Commercialization
Field Testing
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How should equitable or global access be defined?
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What is the scope of confidential information?
What are the obligations of the parties to protect confidential information?
Are there any exceptions to the confidentiality obligations?
Are the parties permitted to make public announcements related to the project?
Can the parties use each other’s name and logo for general marketing materials?
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Under what circumstances can the continuity rights be exercised? (What are the conditions precedent?)
What is an appropriate scope for the continuity rights? What are the rights and obligations of each party?
Should related license grants vest upon execution of the agreement, or at a later stage in development?
Should there be an escrow requirement?
Should there be any restrictions on the developer’s ability to transfer project-related intellectual property to a third party?
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Are there other committees, important governance bodies, or designated individual positions? What are the parties' roles and responsibilities with respect to them?
Are the parties required to meet in accordance with a defined schedule for decision-making and progress reporting activities?
What are the resolution mechanisms for disputes related to the agreement?
Are there any requirements for policies or procedures to manage potential conflicts of interest?
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Are there any circumstances under which one party will not indemnify the other?
What is the process for managing liability claims?
Are there government or other types of indemnification schemes?
Is there any limitation or monetary cap on each party’s liabilities under the agreement?
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What financial and project progress information must be shared between the parties?
What is the required timeline for sharing information?
How is the receiving party permitted to use the information received?
Do the parties have the right to verify the information reported?
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What is the scope of the licensed intellectual property?
What is the territory of the license?
Is the license exclusive or non-exclusive?
Are there any restrictions on the use of the licensed intellectual property?
Are there any specific obligations to exploit the licensed intellectual property?
Can the licensee grant sublicenses to third parties?
Will products manufactured under license be marketed as branded or generic? (i.e. will they bear the licensor’s trademarks/trade dress)
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What are the mechanisms to limit exposure to additional payments or expenses?
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What are the acceptable publication channels?
Is compliance with a specific open access policy required?
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What are the effects of termination or withdrawal by a party?
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Do the parties govern the project through a joint steering committee ("JSC")? If so, what are the parties expressly designated roles and responsibilities with respect to the JSC?
Are there other committees, important governance bodies, or designated individual positions? What are the parties' roles and responsibilities with respect to them?
Are the parties required to meet in accordance with a defined schedule for decision-making and progress reporting activities?
What are the resolution mechanisms for disputes related to the agreement?
Are there any requirements for policies or procedures to manage potential conflicts of interest?
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What occurrences could result in a liability claim against which one party will indemnify the other?
Are there any circumstances under which one party will not indemnify the other?
What is the process for managing liability claims?
Are there government or other types of indemnification schemes?
Is there any limitation or monetary cap on each party’s liabilities under the agreement?
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[description] =>
What financial and project progress information must be shared between the parties?
What is the required timeline for sharing information?
How is the receiving party permitted to use the information received?
Do the parties have the right to verify the information reported?
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[count] => 69
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Are any licenses granted for the use of background or foreground intellectual property?
What is the scope of the licensed intellectual property?
What is the territory of the license?
Is the license exclusive or non-exclusive?
Are there any restrictions on the use of the licensed intellectual property?
Are there any specific obligations to exploit the licensed intellectual property?
Can the licensee grant sublicenses to third parties?
Will products manufactured under license be marketed as branded or generic? (i.e. will they bear the licensor’s trademarks/trade dress)
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[description] =>
[parent] => 48
[count] => 80
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[parent_name] => Intellectual property
[parent_slug] => ip-ownership
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[name] => Payment structures
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[description] => What is the payment structure under this agreement?
What are the mechanisms to limit exposure to additional payments or expenses?
[parent] => 53
[count] => 90
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[parent_slug] => business-model
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[outbreak-preparedness] => WP_Term Object
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[description] =>
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[count] => 13
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[parent_name] => Equitable access
[parent_slug] => access-to-medicines
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[supply-purchase-of-products] => WP_Term Object
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[name] => Product supply
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[description] =>
[parent] => 53
[count] => 45
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[parent_name] => Business model
[parent_slug] => business-model
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[parent] => 0
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[protection-results] => WP_Term Object
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[name] => Protection of IP
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[description] =>
[parent] => 48
[count] => 82
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[parent_slug] => ip-ownership
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[publication-of-results] => WP_Term Object
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[term_id] => 290
[name] => Publication of results
[slug] => publication-of-results
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[taxonomy] => issue
[description] => What information are the parties required or permitted to publish?
What is the required timeline for making data available?
What are the acceptable publication channels?
Is compliance with a specific open access policy required?
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[quality-management] => WP_Term Object
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[name] => Quality management
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[description] =>
[parent] => 53
[count] => 41
[filter] => raw
[parent_name] => Business model
[parent_slug] => business-model
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[regulatory-strategy] => WP_Term Object
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[term_id] => 56
[name] => Regulatory strategy
[slug] => regulatory-strategy
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[taxonomy] => issue
[description] =>
[parent] => 53
[count] => 57
[filter] => raw
[parent_name] => Business model
[parent_slug] => business-model
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[warranties] => WP_Term Object
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[term_id] => 81
[name] => Representations & warranties
[slug] => warranties
[term_group] => 0
[term_taxonomy_id] => 81
[taxonomy] => issue
[description] => Should the parties make any warranties, and if so, what is the scope?
[parent] => 50
[count] => 98
[filter] => raw
[parent_name] => Liability
[parent_slug] => liability
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[technology-transfer] => WP_Term Object
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[term_id] => 86
[name] => Technology transfer
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[term_group] => 0
[term_taxonomy_id] => 86
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[description] => What is included in the technology and/or materials to be transferred?
What are the responsibilities of each party to in relation to the transfer of materials and/or technology?
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[count] => 45
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[term-and-termination] => WP_Term Object
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[description] => Term
What is the term of the agreement? Is it tied to the timeline of the project or license grants?
Termination
Under what circumstances may a party terminate or withdraw from the agreement?
Effects of Termination
What are the effects of termination or withdrawal by a party?
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[count] => 0
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[parent_name] =>
[parent_slug] =>
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[term-of-agreement] => WP_Term Object
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[term_id] => 76
[name] => Term of agreement
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[description] =>
[parent] => 52
[count] => 98
[filter] => raw
[parent_name] => Term & termination
[parent_slug] => term-and-termination
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[termination-and-withdrawal] => WP_Term Object
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[term_id] => 74
[name] => Termination & withdrawal
[slug] => termination-and-withdrawal
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[taxonomy] => issue
[description] =>
[parent] => 52
[count] => 102
[filter] => raw
[parent_name] => Term & termination
[parent_slug] => term-and-termination
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[territory-access-commitments] => WP_Term Object
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[name] => Territory access commitments
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How should ‘territory’ be defined under the agreement? Should the definition make a distinction between different types of purchaser (e.g. public sector vs. private sector)?
Should the developer be required to apply for regulatory approval in priority access markets?
Should the developer be required to commit a proportion of the product manufactured to a certain country or purchasing organization?
Should the developer be required to identify a third party that could fulfill supply requirements for the access territories in the event that the developer does not?
Should the agreement include any anti-diversion provisions?
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[count] => 63
[filter] => raw
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(
)
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