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SBIR Phase I: A cancer diagnostic instrument to measure empirical treatment response

Award Information
Agency: National Science Foundation
Branch: N/A
Contract: 2322382
Agency Tracking Number: 2322382
Amount: $274,930.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: BM
Solicitation Number: NSF 23-515
Solicitation Year: 2023
Award Year: 2023
Award Start Date (Proposal Award Date): 2023-08-01
Award End Date (Contract End Date): 2024-07-31
Small Business Information
7505 Fannin St. Suite 200
Houston, TX 77054
United States
HUBZone Owned: Yes
Woman Owned: Yes
Socially and Economically Disadvantaged: No
Principal Investigator
 David Gallup
 (650) 255-9761
Business Contact
 David Gallup
Phone: (650) 255-9761
Research Institution

The broader impact/commercial potential of this Small Business Innovation Research (SBIR) Phase I project is to improve personalized cancer care by developing a first in class cancer diagnostic instrument that can deliver clinically actionable, personalized, drug response data from individual cancer patients using the E-slice assay.The E-slice assay is a novel 3D culture-based assay which has been shown to accurately predict individual cancer patients’ responses to treatments.The E-slice assay is currently registered as a Clinical Laboratory Improvement Amendments Laboratory Developed Tests (CLIA LDT). The cancer diagnostic market is expected to grow from $56 billion in 2022 to $162 billion by 2027, and this test and automation could capture a significant share of this rapidly expanding market. Beyond improving outcomes for cancer patients, the automation of this assay could have far-reaching implications, such as accelerating and economizing drug screening, discovery, and development for pharmaceutical and biotechnology companies, and academia._x000D_
This Small Business Innovation Research (SBIR) Phase I project addresses the most challenging and risky portion of automating the E-slice assay. The novel engineering solutions that the team proposes to develop will automate the processing of live human tissue samples from a needle biopsy or surgery, generate precision-cut slices, and then precisely position them in a tissue culture plate for downstream culture and analysis.The new device will do so in a manner that maintains sterility, minimizes thermal, chemical, and mechanical stresses, and performs in a highly reliable way.The primary technical challenges are ensuring reliable performance that is equal to or superior than manual methods. The technical milestones include meeting thresholds for reliability, sterility, and tissue viability compared to manual processing._x000D_
This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

* Information listed above is at the time of submission. *

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