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Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- ScitoVation, LLC
- Proposal award date
- 2023-07-07
- Contract end date
- 2024-06-30
- UEI
- MS2HXSWJZJ24
- Solicitation number
- PA22-176
- Topic code
- R
Research abstract
PROJECT SUMMARY
A significant shift in the safety assessment of environmental chemicals is ongoing. This shift includes a reduction,
or in some cases elimination, of traditional toxicity testing in animals with the implementation of new approach
methodologies (NAMs). Although these emerging NAMs provide an attractive means for identifying teratogens
and other developmental toxicants, the absence of a quantitative framework for relating in vitro effects to
equivalent in vivo human exposures limits their use for public health. Here, we develop a tiered approach that
integrates existing pharmacokinetic models for pregnancy into a computational application that can be adapted
to current and emerging NAMs for developmental toxicity. The primary aim of the proposed project is to deliver
an out-of-the-box computational solution for predicting the dose-response of possible human health effects by
performing in vitro-to-in vivo extrapolation (IVIVE). In Specific Aim 1, we will design a web based computational
application, DRIIVE for the Developmental and Reproductive In Vitro to In vivo Extrapolation, that will perform
forward- or reverse-dosimetry using physiologically based pharmacokinetic (PBPK) modeling within a tiered
framework bridging multiple levels of biological complexity. This framework will allow us to better account for
chemical space and exposure routes relevant to environmental toxicants. In Specific Aim 2, the work will
culminate in a case study to take industry-relevant compounds through the defined IVIVE workflows and
compare the outcomes to in-life data. Our proposal will reduce the reliance on current in vivo developmental
toxicity and provide a much-needed framework for the next generation of chemical safety assessment.
Successful completion of this Phase I project will result in a model that will undergo further development and
commercialization in Phase II, with the ultimate goal of providing an IVIVE computational model to our customers.
This developmental toxicity product fits into the existing NAM products that we offer that reduce reliance on
current in vivo animal models.
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.
Research funding history
4 SBIR/STTR records share this UEI (2017–2025). Reported award amounts total $3,210,947. Reported amounts are not federal obligations.
Phases: Phase II, Phase I
Agencies: Department of Health and Human Services
Agency intelligence
Department of Health and Human Services
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