Opportunity Information: Apply for EP PMC 16 001
Apply for EP PMC 16 001
- The HHS-OS-ASPR in the science and technology and other research and development sector is offering a public funding opportunity titled "Combating Antibiotic Resistant Bacteria (CARB) Biopharmaceutical Accelerator" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.360.
- This funding opportunity was created on Feb 17, 2016 and posted on Feb 17, 2016.
- Applicants must submit their applications by Apr 15, 2016. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Each selected applicant is eligible to receive up to $30,000,000.00 in funding.
- The number of recipients for this funding is limited to 2 candidate(s).
- Eligible applicants include: Public and State controlled 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 (see text field entitled Additional Information on Eligibility for clarification).
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Opportunity Summary:
The Combating Antibiotic Resistant Bacteria (CARB) Biopharmaceutical Accelerator grant opportunity (Funding Opportunity Number EP PMC 16 001) is a federal effort to rebuild the early-stage antibacterial drug pipeline in response to the growing threat of antimicrobial resistance. The premise behind the program is that too few promising antimicrobial candidates are moving forward from early proof-of-concept work into the preclinical stage, where they become more attractive for later private investment and eventual clinical development. This opportunity is aligned with the 2014 US National Strategy for Combating Antimicrobial Resistant Bacteria, which called for new ways to stimulate innovation and reduce the scientific and financial barriers that keep early antimicrobial programs from advancing.
The program is structured as a biopharmaceutical accelerator focused only on antibacterial products, not antivirals or antifungals. Its goal is to push candidate antibacterial products through key research and development milestones spanning proof-of-concept through preclinical development. In practical terms, the accelerator is meant to help mature early programs by funding the experiments, studies, and development activities that de-risk a candidate and make it more competitive for follow-on funding and clinical-stage partnerships. The expectation is that products that "graduate" from the accelerator will be in a stronger position to attract additional R and D investment and proceed into clinical development.
A defining feature of this accelerator model is that it is non-equity and provides non-dilutive support. Rather than taking ownership stakes in participating companies or requiring founders to give up control, the model is designed to keep product developers in full ownership and operational control of their organizations. This is intended to make participation attractive to startups and other product developers who might otherwise avoid accelerators or investors that require equity, while still giving them access to resources that can materially advance their programs.
The award mechanism is a cooperative agreement, which generally implies substantial federal involvement during the period of performance compared with a more hands-off grant. The opportunity sits in the Science and Technology and other Research and Development category (CFDA 93.360) and is administered under HHS-OS-ASPR, reflecting the involvement of the Office of the Assistant Secretary for Preparedness and Response. The Biomedical Advanced Research and Development Authority (BARDA) is positioned to provide direct funding, while the National Institute of Allergy and Infectious Diseases (NIAID) contributes in-kind support to strengthen the accelerator's technical capabilities. The in-kind components explicitly include preclinical services and technical expertise, which can be critical for small teams that lack access to specialized testing, animal models, regulatory-quality study design, or translational development know-how.
The intended recipient under the cooperative agreement is an organization that will operate the accelerator and manage a portfolio of investments into early-stage antimicrobial product candidates. In other words, the awardee is not simply advancing one product; it is expected to function as a portfolio manager and accelerator operator that selects, supports, and oversees multiple antibacterial development efforts. This portfolio approach is meant to spread risk across multiple candidates while systematically increasing the number of programs that reach a more investment-ready stage.
Eligibility for this funding is broad and includes public and state-controlled institutions of higher education, private institutions of higher education, nonprofits (including those without 501(c)(3) status, other than higher education institutions), for-profit organizations other than small businesses, small businesses, and additional entity types as described in the full announcement. The government set an award ceiling of $30,000,000 and anticipated making two awards, signaling an intent to fund a small number of accelerator operators at a substantial scale rather than distributing many smaller grants.
Key timeline details in the announcement show it was created and posted on February 17, 2016, with an application closing date of April 15, 2016. Overall, the opportunity is aimed at fixing a specific bottleneck in antibacterial innovation by pairing BARDA funding with NIAID technical support inside a non-dilutive, non-equity accelerator framework, so that more early antibacterial candidates can survive the difficult jump from proof-of-concept to robust preclinical readiness.
Frequently Asked Questions (FAQs): CARB Biopharmaceutical Accelerator (EP PMC 16 001)
What is the CARB Biopharmaceutical Accelerator grant opportunity?
The Combating Antibiotic Resistant Bacteria (CARB) Biopharmaceutical Accelerator (Funding Opportunity Number EP PMC 16 001) is a federal funding opportunity intended to rebuild the early-stage antibacterial drug pipeline. It focuses on moving promising antibacterial candidates from early proof-of-concept work into preclinical development, where they can become more attractive for later private investment and eventual clinical development.
What problem is this program trying to solve?
The program targets a specific bottleneck in antibacterial innovation: too few antimicrobial candidates are progressing from early proof-of-concept into the preclinical stage. By funding key experiments and development activities, the accelerator aims to reduce scientific and financial barriers that prevent early programs from advancing.
How is this opportunity connected to national policy on antimicrobial resistance?
This opportunity aligns with the 2014 US National Strategy for Combating Antimicrobial Resistant Bacteria, which called for new approaches to stimulate innovation and reduce barriers that keep early antimicrobial research programs from moving forward.
Does the accelerator support antivirals or antifungals?
No. The program is structured as a biopharmaceutical accelerator focused only on antibacterial products, not antivirals or antifungals.
What stages of R&D does the accelerator support?
The accelerator is intended to push candidate antibacterial products through key milestones spanning proof-of-concept through preclinical development. In practical terms, it supports the studies and development work that help mature an early program into a more investment-ready, preclinical-ready candidate.
What does it mean that this is an "accelerator" rather than a traditional single-project grant?
The intended recipient is expected to operate the accelerator and manage a portfolio of investments into multiple early-stage antibacterial product candidates. The awardee is not simply advancing one product; it acts as an accelerator operator and portfolio manager that selects, supports, and oversees multiple antibacterial development efforts.
What is meant by a "portfolio approach" in this program?
The awardee is expected to manage a portfolio of antibacterial candidates rather than focusing on a single project. This approach is designed to spread risk across multiple candidates while systematically increasing the number of programs that reach a more investment-ready stage.
What does "non-equity" and "non-dilutive" support mean in this opportunity?
A defining feature of this accelerator model is that it is non-equity and non-dilutive. The model is designed to provide support without taking ownership stakes in participating companies or requiring founders to give up control. Product developers are intended to retain full ownership and operational control of their organizations.
Why is the non-equity model important for participants?
The non-equity, non-dilutive structure is intended to make participation attractive to startups and other developers who might otherwise avoid accelerators or investors that require equity, while still giving them access to resources that can materially advance their antibacterial programs.
What is the award mechanism for this opportunity?
The award mechanism is a cooperative agreement. This generally implies substantial federal involvement during the period of performance compared with a more hands-off grant.
Which federal offices and agencies are involved?
The opportunity is administered under HHS-OS-ASPR (Office of the Assistant Secretary for Preparedness and Response). BARDA (Biomedical Advanced Research and Development Authority) is positioned to provide direct funding, and NIAID (National Institute of Allergy and Infectious Diseases) contributes in-kind support to strengthen the accelerator's technical capabilities.
What kind of support does NIAID provide?
NIAID contributes in-kind support that explicitly includes preclinical services and technical expertise. These resources can be important for teams that lack access to specialized testing, animal models, regulatory-quality study design, or translational development know-how.
What category and CFDA number is associated with this opportunity?
The opportunity is in the Science and Technology and other Research and Development category and is associated with CFDA 93.360.
Who is eligible to apply?
Eligibility is broad and includes public and state-controlled institutions of higher education, private institutions of higher education, nonprofits (including those without 501(c)(3) status, other than higher education institutions), for-profit organizations other than small businesses, small businesses, and additional entity types as described in the full announcement.
Is the awardee expected to be a product developer or an accelerator operator?
The intended recipient is an organization that will operate the accelerator and manage a portfolio of investments into early-stage antibacterial product candidates. The role described is that of an accelerator operator and portfolio manager, not simply a single product developer advancing one candidate.
How much funding is available under this opportunity?
The award ceiling is $30,000,000.
How many awards does the government expect to make?
The government anticipated making two awards, indicating an intent to fund a small number of accelerator operators at substantial scale.
What is the timeline for this opportunity (posting and closing dates)?
The announcement was created and posted on February 17, 2016. The application closing date was April 15, 2016.
What is the core goal for antibacterial candidates supported through the accelerator?
The goal is to push candidates through proof-of-concept and into preclinical development by funding the experiments and development activities that de-risk the product. The expectation is that products that "graduate" from the accelerator will be better positioned to attract follow-on R&D investment and proceed into clinical development.
What is meant by "de-risking" a candidate in this program?
In the context provided, de-risking refers to funding experiments, studies, and development activities that strengthen the evidence base and readiness of a candidate as it moves toward preclinical development, making it more competitive for follow-on funding and clinical-stage partnerships.
What happens after a product "graduates" from the accelerator?
The stated expectation is that products that graduate will be in a stronger position to attract additional R&D investment and proceed into clinical development.
Is this funding designed to be hands-off, or is there federal involvement during the project?
Because the mechanism is a cooperative agreement, it generally implies substantial federal involvement during the period of performance compared with a more hands-off grant.
What makes this opportunity different from equity-based accelerators?
This program emphasizes a non-equity, non-dilutive accelerator framework. Rather than taking ownership stakes, the model is designed to help developers advance candidates while maintaining full ownership and operational control of their organizations.
What is the focus area of the opportunity: broad antimicrobial work or specifically antibacterial development?
The opportunity is specifically focused on antibacterial products and is framed as a response to antimicrobial resistance, with the program structure limited to antibacterial development rather than antivirals or antifungals.
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