Opportunity Information: Apply for RFA HL 17 018
The Core Clinical Centers for the Blood and Marrow Transplant Clinical Trials Network (BMT CTN) (UG1) opportunity is a National Institutes of Health (NIH) cooperative agreement that supports a national, multi-center clinical trials infrastructure focused on hematopoietic stem cell transplantation (HCT), also commonly referred to as blood and marrow transplantation. The grant invites applications from clinical sites (often organized as a single center or a consortium of centers) to serve as "Core Clinical Centers" within the BMT CTN. These funded centers work together to design and run coordinated, multi-site clinical studies that compare new treatment approaches and patient management strategies intended to improve outcomes for both children and adults undergoing HCT. A key emphasis is on efficient, collaborative testing so that promising approaches can be evaluated more quickly and with broader enrollment than a single institution could typically achieve.
The scientific and clinical purpose of the network is to evaluate novel transplant-related interventions across malignant and non-malignant blood diseases, with an explicit interest in studies where HCT is used alone or paired with newer cell-based therapies. In practical terms, the network is positioned to run trials that examine how best to deliver transplantation, prevent or treat complications, refine conditioning regimens, and integrate emerging cellular products into transplant care. During this funding cycle, the FOA highlights flexibility to conduct early-phase, multi-center HCT trials that incorporate novel cell therapies, and to broaden evaluation of promising products from tightly controlled, highly selected patient groups to more heterogeneous, real-world patient populations. That framing signals interest not only in early proof-of-concept studies, but also in moving therapies toward broader applicability, with multi-center participation helping address variability in patients, practices, and outcomes.
This FOA is structured as a cooperative agreement (UG1), meaning NIH has substantial programmatic involvement in the conduct of the funded work compared to a standard research project grant. Awardees are expected to operate as part of a coordinated network that includes the Core Clinical Centers/Consortia, a Data Coordinating Center, and NIH partners including the National Heart, Lung, and Blood Institute (NHLBI) and the National Cancer Institute (NCI), along with other stakeholders. The intent is to create a connected system where trial concepts can be developed, prioritized, launched, and monitored across multiple institutions using harmonized procedures, shared oversight, and centralized coordination for data management and analysis. The end goal is not just to complete trials, but to rapidly disseminate results so they can meaningfully improve clinical practice and strengthen the evidence base for patients who need transplantation therapy.
Eligibility is broad and includes a wide range of domestic U.S. organizations that could support clinical trials activity, such as public and private institutions of higher education, nonprofits (with or without 501(c)(3) status), for-profit organizations (other than small businesses), small businesses, and various levels of government (state, county, city/township, special districts), as well as independent school districts and public housing authorities/Indian housing authorities. The FOA also explicitly calls out additional eligible applicant types such as Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), eligible federal agencies, faith-based or community-based organizations, regional organizations, and tribal governments or tribal organizations (including those other than federally recognized, as specified). Despite the breadth of domestic eligibility categories, foreign entities are not allowed: non-domestic (non-U.S.) organizations cannot apply, non-domestic components of U.S. organizations are not eligible, and foreign components (as defined by NIH policy) are not permitted under this announcement.
Administratively, the opportunity is listed under Funding Opportunity Number RFA-HL-17-018, offered by NIH, and categorized as discretionary funding using the cooperative agreement mechanism. The activity focus is education and health, and the CFDA numbers associated with the program are 93.395 and 93.839. The original posting date in the provided source is 2016-08-18, with an original closing date of 2016-11-10. The announcement does not provide an award ceiling or expected number of awards in the excerpted source data, but the overall structure clearly indicates a network model where multiple clinical centers are selected to participate in a coordinated national trials enterprise.
In summary, this FOA is aimed at building and sustaining the clinical center backbone of the BMT CTN so that high-impact, multi-center HCT and cell-therapy trials can be conducted efficiently, with strong coordination among participating sites and NIH partners. The program is designed to accelerate the evaluation of new transplant and cellular therapy approaches, improve patient outcomes across a range of blood diseases, and ensure that results are disseminated quickly enough to influence standards of care.Apply for RFA HL 17 018
- The National Institutes of Health in the education, health sector is offering a public funding opportunity titled "Core Clinical Centers for the Blood and Marrow Transplant Clinical Trials Network (UG1)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.395, 93.839.
- This funding opportunity was created on 2016-08-18.
- Applicants must submit their applications by 2016-11-10. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For-profit organizations other than small businesses, Small businesses, Others.
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Frequently Asked Questions (FAQs)
What is this funding opportunity?
This opportunity supports the Core Clinical Centers for the Blood and Marrow Transplant Clinical Trials Network (BMT CTN) under a UG1 cooperative agreement mechanism. It funds a national, multi-center clinical trials infrastructure focused on hematopoietic stem cell transplantation (HCT), also known as blood and marrow transplantation.
What is the official Funding Opportunity Number (FOA number)?
The Funding Opportunity Number is RFA-HL-17-018.
Which federal agency is offering this opportunity?
The opportunity is offered by the National Institutes of Health (NIH).
What does it mean that this is a UG1 cooperative agreement?
A UG1 is a cooperative agreement, which means NIH has substantial programmatic involvement in the conduct of the funded work compared to a standard research project grant. Funded sites are expected to operate as part of a coordinated network with shared oversight and centralized coordination.
What is the BMT CTN trying to accomplish through this program?
The network is designed to efficiently design and run coordinated, multi-site clinical studies that compare new treatment approaches and patient management strategies to improve outcomes for children and adults undergoing HCT. A central goal is to evaluate promising approaches faster and with broader enrollment than a single institution can typically achieve, and to disseminate results rapidly to influence clinical practice.
Who should apply to be a "Core Clinical Center"?
The FOA invites applications from clinical sites, which are often organized as a single center or a consortium of centers, to serve as Core Clinical Centers within the BMT CTN. These centers function as part of the network’s clinical backbone for multi-site trials.
Are consortia allowed, or must an application come from a single center?
Applications may come from a single center or a consortium of centers, based on how the clinical site is organized.
What kinds of studies will the network conduct?
The network conducts multi-center clinical studies in HCT that compare new treatment approaches and patient management strategies, including trials to refine conditioning regimens, prevent or treat complications, and integrate emerging cellular products into transplant care.
Which patient populations are included in the program’s scope?
The program’s clinical studies are intended to improve outcomes for both children and adults undergoing hematopoietic stem cell transplantation.
What diseases or conditions are within scope for these trials?
The network’s purpose includes evaluating novel transplant-related interventions across malignant and non-malignant blood diseases.
Does the FOA include interest in cell-based therapies?
Yes. The FOA explicitly notes interest in studies where HCT is used alone or paired with newer cell-based therapies, and it highlights flexibility to conduct early-phase, multi-center HCT trials that incorporate novel cell therapies.
Is this focused only on early-phase trials, or also on broader populations?
The FOA highlights flexibility to conduct early-phase, multi-center HCT trials incorporating novel cell therapies and also emphasizes broadening evaluation of promising products from highly selected patient groups to more heterogeneous, real-world patient populations.
How is the BMT CTN organized under this opportunity?
The network includes Core Clinical Centers/Consortia, a Data Coordinating Center, and NIH partners, including the National Heart, Lung, and Blood Institute (NHLBI) and the National Cancer Institute (NCI), along with other stakeholders.
What is the role of the Data Coordinating Center in this network model?
The FOA describes a centralized coordination approach that includes data management and analysis across multiple institutions, supported through a Data Coordinating Center as part of the coordinated network structure.
What kinds of coordination and standardization are expected across participating sites?
The network model emphasizes harmonized procedures, shared oversight, and centralized coordination so trial concepts can be developed, prioritized, launched, and monitored across multiple institutions.
What is the intended benefit of conducting trials through a national multi-center network?
The network approach is meant to enable efficient, collaborative testing with broader enrollment and multi-center participation, helping evaluate therapies more quickly and address variability in patients, practices, and outcomes compared to single-institution efforts.
What is the activity focus area of this opportunity?
The activity focus is education and health.
What are the CFDA numbers associated with this program?
The CFDA numbers listed are 93.395 and 93.839.
What types of U.S. organizations are eligible to apply?
Eligibility is broad and includes domestic U.S. public and private institutions of higher education; nonprofits (with or without 501(c)(3) status); for-profit organizations (other than small businesses); small businesses; and various levels of government (state, county, city/township, special districts), as well as independent school districts and public housing authorities/Indian housing authorities.
Are minority-serving institutions and tribal entities eligible?
Yes. The FOA explicitly identifies eligible applicant types including Alaska Native and Native Hawaiian Serving Institutions, AANAPISIs, Hispanic-serving Institutions, HBCUs, TCCUs, tribal governments or tribal organizations (including those other than federally recognized, as specified), and other listed domestic categories.
Are faith-based or community-based organizations eligible to apply?
Yes. Faith-based or community-based organizations are explicitly included among eligible applicant types.
Are federal agencies eligible to apply?
Yes. Eligible federal agencies are explicitly listed among eligible applicant types.
Are foreign organizations allowed to apply?
No. Non-domestic (non-U.S.) organizations cannot apply under this announcement.
Can a U.S. organization include non-U.S. components or foreign components in the application?
No. Non-domestic components of U.S. organizations are not eligible, and foreign components (as defined by NIH policy) are not permitted under this announcement.
When was this opportunity originally posted, and what was the original closing date?
The original posting date listed is 2016-08-18, and the original closing date listed is 2016-11-10.
Does the provided information include an award ceiling or the expected number of awards?
No. The excerpted source data does not provide an award ceiling or an expected number of awards.
What is the main deliverable expected from funded Core Clinical Centers?
Funded centers are expected to work together within the BMT CTN to design, run, and monitor coordinated multi-site clinical trials in HCT and related cellular therapy integration, and to support rapid dissemination of results to strengthen the evidence base and improve standards of care.
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