SBIR/STTR Research Award

Establishment of a First-in-Class Biocompatible and Efficient Cryopreservation Technology Platform for the Next Generation of Cell-Based Therapeutics in Regenerative Medicine and Drug Discovery

Award identifier 1d00fe3da168783a9dce65471cc21e41e97346f5915335dff8750b1e7c57720bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,863,241

Program and phase

SBIR · Phase II

Award year

2024

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CRYOCRATE LLC
Proposal award date
2024-09-15
Contract end date
2026-08-31
UEI
MXHXWLBMUZL7
Solicitation number
PA22-176
Topic code
100

Research abstract

SUMMARY Previous support from NIH SBIR and Coulter Foundation awards allowed the CryoCrate team to develop a first- in-class biocompatible cryopreservation medium product, trademarked as OdinSol®, that provides enabling and efficient options for biobanking urgently needed for the development and implementation of cell-based therapeutics and tissue engineering in personalized medicine. The OdinSol® technology removes the need for any toxic cell permeating cryoprotectant used in nearly all existing cryopreservation methods, secures long-term storage in regular -80oC deep freezers, and significantly improves the cryopreservation efficiency for cell-based therapeutic materials (e.g., iPSC-derived cells or tissues). Based on our former experience in FDA 510(k) submission, in this project, we organized the collaboration with our regulatory consultant (Cardinal Health), contract manufacturing organizations (Bryllan), contract research organization (WuXi AppTec), academic co-inventor (University of Missouri – Kansas City Vision Research Center), to achieve the following milestones: I. The production of OdinSol® meets GMP qualifications and biocompatibility assessment shows compliance with FDA guidance for 510(k) submission as a storage device for transplantable tissues; II. The in vitro and in vivo evaluation of safety and efficacy demonstrates the OdinSol® technology to be superior to existing cryopreservation protocols with respect to preserving viability and function of novel cell-based therapeutic materials for regenerative medicine; III. Based on those qualifications, we will complete of the 510(k) submission and finalize of the production line based on further FDA feedback before the end of the project period. We expect future clinical use of the OdinSol® technology within three years after the FDA clearance, providing the regenerative medicine industry with a highly efficient biocompatible cryostorage platform.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

9 SBIR/STTR records share this UEI (2015–2024). Reported award amounts total $9,178,721. Reported amounts are not federal obligations.

Phases: Phase I, Phase II – Direct to Phase II, Phase II

Agencies: Department of Health and Human Services, Department of Agriculture

Agency intelligence

Department of Health and Human Services

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