2024 NIAID Omnibus Broad Agency Announcement HHS-NIH-NIAID-BAA2024-1 Now Available
Notice Number:
NOT-AI-24-014

Key Dates

Release Date:

December 22, 2023

Related Announcements

None

Issued by

National Institute of Allergy and Infectious Diseases (NIAID)

Purpose

The National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), of the Department of Health and Human Services (DHHS) supports research related to the basic understanding of microbiology and immunology leading to the development of vaccines, therapeutics, and medical diagnostics for the prevention, treatment, and diagnosis of infectious and immune-mediated diseases.  This Broad Agency Announcement is soliciting proposals that possess the research and development (R&D) expertise necessary for successfully carrying out research toward meeting the program objectives of the Division of Microbiology and Infectious Diseases (DMID), NIAID, NIH.

The Omnibus BAA is governed by Federal Acquisition Regulation (FAR) 6.102(d)(2) and FAR 35.016, as well as the NIH Policy Manual, Manual Chapter 6035, Broad Agency Announcements. A BAA may be used as a solicitation mechanism for basic and applied research directed toward advancing the state-of-the-art or increasing knowledge or understanding and that part of development not related to the development of a specific system or hardware procurement. BAAs are general in nature, identifying areas of research interest, and shall only be used when meaningful proposals with varying technical/scientific approaches can be reasonably anticipated.

Offers submitted in response to this BAA will be required to present separate detailed technical and business proposals designed to meet the Technical Objectives described for each Research Area proposed. The Statement of Work (SOW), including the specific technical requirements and performance specifications, shall be developed and proposed by the Offeror, not the Government.

Proposals received in response to this BAA are NOT evaluated against each other since they are not submitted in accordance with a common SOW issued by the Government. Instead, Research and Technical Objectives will be provided in the BAA that describe individual Research Areas in which the Government is interested. Proposals received in response to the BAA will be evaluated in accordance with the Evaluation Factors for Award specified in the announcement. The Government reserves the right to conduct discussions with all, some, one, or none of the proposals received in response to this BAA. If discussions are conducted, the Government reserves the right to suggest modifying, adding or deleting milestones, decision points, research plans, processes, schedules, budget or product. The Government also reserves the right to make awards without discussions. Additionally, the Government reserves the right to accept proposals in their entirety or to select only portions of proposals for award. Multiple awards are anticipated. Selection for award under this BAA will be based upon the evaluation factors, importance to the agency programs, and the availability of funds.

The Research Areas included in this NIAID DMID OMNIBUS BROAD AGENCY ANNOUNCEMENT No. HHS-NIH-NIAID-BAA2024-1, as well as the projected amounts of available funding, are discussed below.

Research Areas 001, 002, and 003: For FY 25, the NIAID estimates up to $16 million for the award of 5 cost reimbursement type base contracts across all three Research Areas (001, 002 & 003). The estimated FY 25 funding is for the non-severable Base Requirement (direct and indirect costs combined) only. If options are proposed by an Offeror, they will be evaluated in accordance with Section 6 of the BAA. The number of awarded contracts will depend on the number of technically meritorious proposals, agency priorities, and availability of funds.

DIVISION OF MICROBIOLOGY AND INFECTIOUS DISEASES (DMID), NIAID, NIH

Research Area 001: Vaccine Candidates

The goal of Research Area 001 is to protect human health and well-being by advancing specific vaccine candidates that utilize technology platforms that ideally elicit a rapid onset of immunity following a single dose, provide a durable response and are readily adaptable to multiple emerging pathogens.  These vaccine technologies and platforms may include, but are not limited to, any of the following: novel adjuvant vaccine formulations, delivery platforms that are scalable or produce mucosal immunity, nucleic acid-based platforms, viral vectors, and nanoparticle/VLP approaches.

Research Area 002: Therapeutic Candidates

The objective of Research Area 002 is the development of new therapeutic products for diseases caused by specific viral, bacterial and fungal pathogens and their drug resistant variants in the following list:

  • Viral Hemorrhagic Fever viruses (e.g., https://www.cdc.gov/vhf/index.html)
  • Coronaviruses, targeting a novel mechanism of action (MOA) different from SARS-CoV-2 approved drugs or with demonstrated pan-coronavirus activity
  • Pseudomonas aeruginosa
  • Candida auris, Aspergillus fumigatus or Mucorales 

Important notice to Offerors: Research Area 002 only supports development of therapeutic products.

“Therapeutic” activity refers to elimination or substantial reduction of infective pathogens by administration of a pharmaceutical agent after challenge. “Pan-coronavirus” activity requires demonstrated SARS-CoV-1, SARS-CoV-2 and MERS-CoV activity.

A candidate therapeutic may be a lead series, a preclinical candidate, or a clinical candidate. The product must be based on a small molecule (e.g., natural products, nucleosides, oligonucleotides or peptides) or bacteriophages. The following are not included: proteins, monoclonal antibodies, other biologic entities (except bacteriophages), and conjugates of such entities. 

Research Area 003: In Vitro Diagnostics

NIAID is interested in supporting the development of promising diagnostics technologies in three areas for detection of signatures from biothreat pathogens and toxins, as well as pathogens causing emerging, reemerging, antimicrobial resistant infectious diseases, and for pandemic preparedness.

  1. Untargeted (Agnostic) and Targeted Nucleic Acid Sequencing on Portable or Laboratory-Automated Systems

    The first objective of Research Area 003 is to improve the overall performance of nucleic acid sequencing solutions on portable or laboratory-automated commercial sequencing platforms for the targeted or agnostic detection and identification of viral pathogens for biodefense, emerging infectious diseases, and pandemic preparedness.
     
  2. Multiplex Protein or Nucleic Acid Detection in Near-Patient Testing Systems

    The second objective of Research Area 003 is to develop methods that improve pathogen analyte detection in one of two ways:

    • First, protein technology improvements such as protein sequencing or mass spectrometry, especially in ways that bring protein-identification testing nearer to the patient; or near-patient rapid antigen testing improvements for rapid and highly sensitive toxin or other protein detection; or solutions for rapid development of synthetic binding moieties for capture of novel proteins.  The emphasis here is on methods improvement in time and analytical sensitivity.
       
    • Second, multiplex nucleic acid detection that is near-patient, rapid, low-complexity, low-cost, and sensitive for detection of sexually transmitted infections.  Design and development can be for testing from care provider-collected or self-collected specimens.  The emphasis here is on expanded breadth of infectious pathogens detected, especially, but not limited to, those identifiable from genital ulcer diagnostic (GUD) testing.
       
  3. Bacterial Identification and Phenotypic Antimicrobial Resistance Characterization

    The third objective of Research Area 003 is to improve direct-from-blood or other biofluid detection and identification of microbial infection coupled with phenotypic antibiotic susceptibility testing (AST) characterization.

Contract Proposal Receipt Date:

Proposals submitted in response to the BAA Solicitation must be received by 3:00 p.m. Eastern Standard Time on March 12, 2024.

Any responsible offeror may submit a proposal which shall be considered by the Agency. For this solicitation, the NIAID requires proposals to be submitted online via the NIAID electronic Contract Proposal Submission (eCPS) website. Submission of proposals by facsimile or e-mail is not acceptable.

For directions on using eCPS, go to the website: https://ecps.nih.gov and then click on "How to Submit."

Inquiries

Please direct all inquiries to:

Alexandra Buck, JD
Contracting Officer
Research Contracts Branch-A (MIDRCB-A)
Office of Acquisitions, DEA, NIAID, NIH, HHS
Email:   [email protected]