BARDA DRIVe EZ-BAA (EZBAA - 22-100-SOL-00003)

Location: Minnesota
Posted: Apr 27, 2026
Agency: HEALTH AND HUMAN SERVICES, DEPARTMENT OF
Type of Contract: Awards
Type of Government: Federal
Category:
  • A - Research and development
Solicitation No: 75A50126C00005
Publication URL: To access bid details, please log in.
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BARDA DRIVe EZ-BAA (EZBAA - 22-100-SOL-00003)
Active
Contract Opportunity
Notice ID
75A50126C00005
Related Notice
DRIVeEZBAA22100SOL00003
Contract Line Item Number
CLIN0001
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
Award Details
  • Contract Award Date: Apr 27, 2026
  • Contract Award Number: 75A50126C00005
  • Task/Delivery Order Number:
  • Contractor Awarded Unique Entity ID: M3QDM72NME75
  • Contractor Awarded Name: ISOLA THERAPEUTICS INC
  • Contractor Awarded Address: Minneapolis , MN 55410 USA
  • Base and All Options Value (Total Contract Value): $7,485,416.99
General Information
  • Contract Opportunity Type: Award Notice (Original)
  • Original Published Date: Apr 27, 2026 11:01 am EDT
  • Inactive Policy: 15 days after contract award date
  • Original Inactive Date: May 12, 2026
  • Initiative:
    • None
Classification
  • Original Set Aside:
  • Product Service Code: AN13 - HEALTH R&D SERVICES; HEALTH CARE SERVICES; EXPERIMENTAL DEVELOPMENT
  • NAICS Code:
    • 541714 - Research and Development in Biotechnology (except Nanobiotechnology)
  • Place of Performance:
    Minneapolis , MN 55410
    USA
Description

The purpose of the proposed Contract is for Nebulization Therapy to Prevent and Treat Pulmonary Foam Caused by Inhaled Chemical Agents.



The primary goal of the R&D effort described in this statement of work (SOW) is to generate the necessary data and information to support an initial FDA meeting to align on the regulatory strategy. The contract scope includes early-stage formulation and analytical development of the drug product; nebulizer characterization including flow rates and particle size distribution; bioanalytical development to support non-GLP studies using the proposed test article including PK, dose range finding, and chlorine exposure proof-of-concept (POC); and development of an overall regulatory strategy. This scope of work is expected to support a productive FDA engagement and advance the technical readiness level (TRL) through TRL 5 to meet minimum requirements to support various future contract vehicles. The generated data and completed non-GLP studies, along with FDA feedback, will inform work required in later development phases.


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Contact Information
Contracting Office Address
  • O’NEILL HOUSE OFFICE BUILDING
  • WASHINGTON , DC 20515
  • USA
Primary Point of Contact
Secondary Point of Contact
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