RRPV BoNT-NMJ

Location: District of Columbia
Posted: Apr 20, 2026
Due: May 11, 2026
Agency: HEALTH AND HUMAN SERVICES, DEPARTMENT OF
Type of Government: Federal
Category:
  • 65 - Medical, Dental, and Veterinary Equipment and Supplies
Solicitation No: SSN-BARDA-04202026
Publication URL: To access bid details, please log in.
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RRPV BoNT-NMJ
Active
Contract Opportunity
Notice ID
SSN-BARDA-04202026
Related Notice
Department/Ind. Agency
HEALTH AND HUMAN SERVICES, DEPARTMENT OF
Sub-tier
OFFICE OF ASSISTANT SECRETARY FOR PREPAREDNESS AND RESPONSE
Office
BARDA - ASPR / DAAPPO / BARDA DCMA
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General Information
  • Contract Opportunity Type: Sources Sought (Original)
  • Original Published Date: Apr 20, 2026 09:39 am EDT
  • Original Response Date: May 11, 2026 01:00 pm EDT
  • Inactive Policy: 15 days after response date
  • Original Inactive Date: May 26, 2026
  • Initiative:
    • None
Classification
  • Original Set Aside:
  • Product Service Code: 6505 - DRUGS AND BIOLOGICALS
  • NAICS Code:
    • 541714 - Research and Development in Biotechnology (except Nanobiotechnology)
  • Place of Performance:
    Washington , DC
    USA
Description

Botulinum neurotoxins (BoNT/A–G) inhibit acetylcholine release at the neuromuscular junction through cleavage of SNARE proteins (e.g., SNAP-25, VAMP, syntaxin). Currently, BoNT characterization, including toxin potency and neutralization by medical countermeasures, is measured using mouse-based bioassays, primarily the Mouse Potency Assay (MPA) and Mouse Neutralization Assay (MNA), respectively.



There is increasing scientific, ethical, and regulatory interest in transitioning to human-relevant in vitro systems that can provide mechanistic insight while reducing reliance on animal testing. NMJ micro-physiological systems may provide a biologically relevant platform capable of measuring BoNT potency and evaluating countermeasure efficacy.



BARDA is interested in understanding whether NMJ-based in vitro platforms could support future development of validated assays capable of reducing and potentially replacing reliance on mouse bioassays for BoNT potency and neutralization measurements, with specific interest in systems that can show recovery of neuronal signaling and thereby be appropriate for medical countermeasures evaluation.


Attachments/Links
Contact Information
Contracting Office Address
  • O’NEILL HOUSE OFFICE BUILDING
  • WASHINGTON , DC 20515
  • USA
Primary Point of Contact
Secondary Point of Contact
History
  • Apr 20, 2026 09:39 am EDTSources Sought (Original)
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