Opportunity ID: 316196

General Information

Document Type: Grants Notice
Funding Opportunity Number: RFA-GM-19-001
Funding Opportunity Title: Methods to Improve Reproducibility of Human iPSC Derivation, Growth and Differentiation (SBIR) (R44 Clinical Trial Not Allowed)
Opportunity Category: Discretionary
Opportunity Category Explanation:
Funding Instrument Type: Grant
Category of Funding Activity: Education
Environment
Food and Nutrition
Health
Category Explanation:
Expected Number of Awards:
Assistance Listings: 93.113 — Environmental Health
Cost Sharing or Matching Requirement: No
Version: Synopsis 1
Posted Date: May 21, 2019
Last Updated Date: May 21, 2019
Original Closing Date for Applications: Jan 06, 2020
Current Closing Date for Applications: Jan 06, 2020
Archive Date: Feb 11, 2020
Estimated Total Program Funding:
Award Ceiling: $375,000
Award Floor:

Eligibility

Eligible Applicants: Small businesses
Additional Information on Eligibility: Other Eligible Applicants include the following: Non-domestic (non-U.S.) Entities (Foreign Institutions) are not eligible to apply. Non-domestic (non-U.S.) components of U.S. Organizations are not eligible to apply. Foreign components, as defined in the NIH Grants Policy Statement, may be allowed.

Additional Information

Agency Name: National Institutes of Health
Description: Human induced pluripotent stem cells (iPSCs) have been used with great success to mimic the differentiation of a variety of tissues, understand early development and study human diseases. Despite approaches that have made the derivation, growth and differentiation of iPSCs more efficient, there remains significant variability in reprogramming efficacy, genomic integrity and developmental potential of iPSCs derived from a single fibroblast or tissue sample. Thus, iPSCs derived from the same sample may differ in their in vitro growth characteristics and their ability to re-differentiate into the desired tissue type. A variety of issues may affect derivation of the iPSCs and their growth, stability and differentiation, including the specific characteristics of the starting cell or tissue sample (e.g., age of donor, tissue type and anatomical location, physiological and disease state), the methods and protocols used to induce pluripotency (e.g., transcription factors, small molecules, cell fusion), the choice of growth factors and other culture conditions, method of storage of cell lines, etc. Further challenges include growing and maintaining sufficient quantities of iPSC lines in culture without changes in their properties, as well as the ability of multiple investigators to identify and authenticate iPSC lines as part of their research. This Funding Opportunity Announcement (FOA) will support SBIR projects to develop novel, reliable and cost-effective methods to standardize and increase the utility and reproducibility of iPSCs at all stages, from their derivation to their research and clinical applications.
Link to Additional Information: http://grants.nih.gov/grants/guide/rfa-files/RFA-GM-19-001.html
Grantor Contact Information: If you have difficulty accessing the full announcement electronically, please contact:

NIH OER Webmaster
FBOWebmaster@OD.NIH.GOV
Email:FBOWebmaster@OD.NIH.GOV

Version History

Version Modification Description Updated Date

Related Documents

Packages

Agency Contact Information: NIH OER Webmaster
FBOWebmaster@OD.NIH.GOV
Email: FBOWebmaster@OD.NIH.GOV
Who Can Apply: Organization Applicants

Assistance Listing Number Competition ID Competition Title Opportunity Package ID Opening Date Closing Date Actions
FORMS-E FORMS-E PKG00251179 Dec 06, 2019 Jan 06, 2020 View

Package 1

Mandatory forms

316196 RR_SF424_2_0-2.0.pdf

316196 PHS398_CoverPageSupplement_4_0-4.0.pdf

316196 RR_OtherProjectInfo_1_4-1.4.pdf

316196 PerformanceSite_2_0-2.0.pdf

316196 RR_KeyPersonExpanded_2_0-2.0.pdf

316196 RR_Budget_1_4-1.4.pdf

316196 PHS398_ResearchPlan_4_0-4.0.pdf

316196 SBIR_STTR_Information_1_2-1.2.pdf

Optional forms

316196 RR_SubawardBudget30_1_4-1.4.pdf

316196 PHS_AssignmentRequestForm_2_0-2.0.pdf

2025-07-09T16:43:49-05:00

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