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Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- SANARIA INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- YLF2SS2NYGC5
- Solicitation number
- PA11-096
- Topic code
- NIAID
Research abstract
DESCRIPTION provided by applicant The ideal tool for eliminating Plasmodium falciparum Pf the causative agent of of all malaria deaths would be a highly effective vaccine that prevents blood stage infection and thereby prevents the disease and transmission The only immunogens demonstrated in humans to be able to induce andgt protective efficacy that is sustained months are PfSPZ Sanariaandapos s goal is to develop and commercialize a Pf sporozoite SPZ vaccine that prevents Pf blood stage infection in andgt of recipients The SanariaTM PfSPZ Vaccine is composed of aseptic attenuated purified cryopreserved PfSPZ The platform technology developed to manufacture the PfSPZ Vaccine has facilitated manufacture of PfSPZ for infection of volunteers to test vaccines and drugs PfSPZ Challenge and for vaccination with PfSPZ Challenge under chloroquine protection PfSPZ CVac These three products are on an aggressive timeline to commercialization with clinical trials in countries on continents planned for the next months two of which are in progress All of these external clinical trialsandapos efforts are funded by our collaborators due to their enthusiasm for
these products This includes the first trials ever funded by an African government When Sanaria was established many in the field considered it impossible to manufacture aseptic purified vialed cryopreserved PfSPZ that would meet regulatory standards When this was achieved under the first Phase II SBIR of this grant it was argued that PfSPZ could not be manufactured to meet cost of goods standards In the Competitive Renewal of that Phase II SBIR for which we report our Key Results herein we made substantial progress toward reducing cost of goods by innovatively improving the efficiency of manufacturing and release assays Based on that progress we have designed a manufacturing facility to be built within our current space that based on conservative estimates will manufacture doses year of x PfSPZ dose at andlt $ dose We previously thought the new facility would have to be at a different site cost $ M and require years to design build and validate Based on our innovations success in the clinic and lab and the increased demand by the malaria community for what is now a range of PfSPZ products we re designed the facility as an extension of our current Clinical Manufacturing Facility Taking advantage of existing infrastructure and resources it can be built at a cost of $ M and be operational in andlt years from initiation of the project In thi new Competitive Renewal Proposal we will establish the innovations to allow full integration of the scaled up process steps for manufacture of PfSPZ products in the new facility We will translate our innovations and advances into a robust process at a higher scale including refining the equipment tools and processes at each step months Preliminary integration months will be followed by a finalized process in the new facility months This will further reduce cost of goods for all of Sanariaandapos s PfSPZ based products and accelerate widespread use and sales distribution to those who most need a malaria vaccine
PUBLIC HEALTH RELEVANCE Malaria causes million clinical cases and nearly million deaths annually is responsible for andgt loss of GDP in Africa annually and is a serious concern for travelers and military personnel Sanariaandapos s goal is to develop and commercialize a andgt protective malaria vaccine for three primary markets with a potential for andgt $ billion annual revenues Travelers from the developed world to malaria endemic areas military personnel and geographically focused elimination campaigns are the initial markets The eventual goal though continues to be infants and young children in the developing world and eventual eradication of the disease Success in this Phase II SBIR renewal will leave Sanaria ideally placed to design and implement an enhanced manufacturing facility in which the companyandapos s malaria vaccine can be optimally manufactured for pivotal Phase studies licensure and commercial launch
Malaria causes million clinical cases and nearly million deaths annually is responsible for andgt loss of GDP in Africa annually and is a serious concern for travelers and military personnel Sanariaandapos s goal is to develop and commercialize a andgt protective malaria vaccine for three primary markets with a potential for andgt $ billion annual revenues Travelers from the developed world to malaria endemic areas military personnel and geographically focused elimination campaigns are the initial markets The eventual goal though continues to be infants and young children in the developing world and eventual eradication of the disease Success in this Phase II SBIR renewal will leave Sanaria ideally placed to design and implement an enhanced manufacturing facility in which the companyandapos s malaria vaccine can be optimally manufactured for pivotal Phase studies licensure and commercial launch
Technology keywords
Not reported
Other awards by this recipient
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Awards with the same topic code
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Research funding history
61 SBIR/STTR records share this UEI (2003–2024). Reported award amounts total $99,330,850. Reported amounts are not federal obligations.
Phases: Phase I, Phase II, Phase II – Direct to Phase II
Agencies: Department of Health and Human Services, Department of Defense
Agency intelligence
Department of Health and Human Services
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