Key Dates
NOT-RM-22-006 - Notice of Intent to Publish a Funding Opportunity Announcement for Somatic Cell Genome Editing Translational Coordination and Dissemination Center (U24, Clinical Trial Not Allowed)
NOT-RM-22-007 - Notice of Intent to Publish a Funding Opportunity Announcement for Technologies and Assays for Therapeutic Genome Editing INDs (U01, Clinical Trial Not Allowed)
NOT-RM-22-009 - Notice of Intent to Publish a Funding Opportunity Announcement for Platform Clinical Trials of Somatic Genome Editing for Multiple Diseases (UG3/UH3, Clinical Trial Required)
Office of Strategic Coordination (Common Fund)
The Somatic Cell Genome Editing (SCGE) program from the NIH Common Fund intends to issue Funding Opportunity Announcements (FOAs) for the second phase (FY2023-2027) of the program. In Phase 2 the SCGE program will accelerate the development of genome editing therapeutic agents by: facilitating Investigational New Drug (IND) application enabling studies; establishing pathways to regulatory approval; and disseminating successful strategies for initiating first in human clinical trials.
SCGE Phase 2 will include four FOAs: 1) an initiative for the development of technology/assays that support IND-submissions, 2) another for optimizing genome editing-based therapeutic leads for safety and efficacy, 3) a platform clinical trials initiative using genome editing therapeutics for more than one disease, 4) and a Translational Coordination and Dissemination Center (TCDC). Together these initiatives will comprise a consortium that will accelerate the optimization of promising clinical candidates toward IND filings and first in human clinical trials.
This Notice is being provided to allow potential applicants to the FOA for optimizing genome editing-based therapeutic leads for safety and efficacy sufficient time to develop meaningful collaborations and responsive projects.
The FOA is expected to be published in Spring 2022 with expected application due dates in Summer 2022.
Details are provided below.
Background
The NIH Somatic Cell Genome Editing (SCGE) program is funded through the NIH Common Fund, which supports cross-cutting programs that are expected to have exceptionally high impact. All Common Fund initiatives invite investigators to develop bold and innovative approaches to address problems that may seem intractable or to seize new opportunities that offer the potential for transformation of research processes.
The simplicity and broad applicability of targeted and programmable genome editing approaches, including but not limited to those based on CRISPR-Cas9, raise the possibility of a fundamentally new way to treat a variety of genetic diseases. However, many challenges need to be overcome before such techniques could be widely used in the clinic. To maximize the potential of genome editing technology, the SGCE program was developed to accelerate the translation of genome editing technology into clinical applications.
Based on input received from stakeholders from academia, industry, and regulatory agencies, as well as the substantial progress in the field of genome editing since the launch of the first five-year phase of the SCGE program, the second five-year phase of SCGE will focus on translating and accelerating safe and effective genome editing therapeutics into the clinic. Specifically, SCGE Phase 2 will support the following initiatives: 1) Technologies and Assays for Therapeutic Genome Editing INDs; 2) IND-enabling Studies of Somatic Genome Editing Therapeutic Leads; 3) Platform Clinical Trials of Somatic Genome Editing for Multiple Diseases and 4) Somatic Cell Genome Editing Translational Coordination and Dissemination Center.
The SCGE program will involve collaborative research by a consortium of grantees with differing expertise to develop, optimize and demonstrate genome editing technologies as treatments for human disease. Awardees from all four SCGE program components will form a consortium, governed by a steering committee of investigators and NIH staff that will develop consensus policies and procedures for Consortium-wide activities such as data and resource sharing. Collectively, these initiatives are intended to substantially expand the number of genetic diseases treated by in vivo genome editing, ultimately allowing these technologies to achieve their potential as a therapeutic platform to treat genetic disease.
IND-enabling Studies of Somatic Genome Editing Therapeutic Leads
Phase II of the SCGE program will include a funding announcement for IND-enabling Studies of Somatic Genome Editing Therapeutic Leads (U19, Clinical Trial Not Allowed). The goal of this U19 FOA is to support team-based research projects to accelerate further optimization and development of genome editing-based therapeutic leads towards IND-enabling studies and an IND submission to the U.S. Food and Drug Administration (FDA). The proposed leads should demonstrate strong biological rationale and in vitro and/or in vivo proof of concept (POC) data generated in model system(s) each defined by the targeted cell or tissue type to establish a genome editing therapeutic approach that is potentially adaptable to target different pathogenic variants in the same cell or tissue types.
TBD
- Pending availability of funds, estimated total funding is $25 mil per year in FY23-FY27.
- 5 awards
- TBD
- TBD
Private Institution of Higher Education
Nonprofit with 501(c)(3) IRS Status (Other than Institution of Higher Education)
Small Business
For-Profit Organization (Other than Small Business)
State Government
Indian/Native American Tribal Government (Federally Recognized)
County governments
Independent school districts
Public housing authorities/Indian housing authorities
Indian/Native American Tribally Designated Organization (Native American tribal organizations (other than Federally recognized tribal governments)
U.S. Territory or Possession
Indian/Native American Tribal Government (Other than Federally Recognized)
Regional Organization
Applications are not being solicited at this time.
Please direct all inquiries to:
Chris Boshoff, Ph.D.
National Institute of Neurological Disorders and Stroke (NINDS)
301-496-1779
and Human Services (HHS)
