Bundibugyo Virus Outbreak Response Vaccines (BundiVx) - RRPV Consortium

Project Information

Bid Title
Bundibugyo Virus Outbreak Response Vaccines (BundiVx) - RRPV Consortium
Issuing Agency
Location
District of Columbia
Published Date
Jun 18, 2026
Closing Date
Jul 2, 2026
Government Level
Federal
Status
Closed
Ref. #
RRPV-26-13-BundiVx
Original Source
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Set Aside
No Set aside used
Project Description
Follow
Bundibugyo Virus Outbreak Response Vaccines (BundiVx) - RRPV Consortium
Active
Contract Opportunity
Notice ID
RRPV-26-13-BundiVx
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 View Changes
  • Contract Opportunity Type: Solicitation (Updated)
  • Updated Published Date: Jun 18, 2026 08:17 am EDT
  • Original Published Date: Jun 11, 2026 01:18 pm EDT
  • Updated Date Offers Due: Jul 02, 2026 01:00 pm EDT
  • Original Date Offers Due: Jun 26, 2026 03:00 pm EDT
  • Inactive Policy: 15 days after date offers due
  • Updated Inactive Date: Jul 17, 2026
  • Original Inactive Date: Jul 11, 2026
  • Initiative:
    • None
Classification
  • Original Set Aside: No Set aside used
  • Product Service Code: AN23 - HEALTH R&D SERVICES; HEALTH RESEARCH AND TRAINING; EXPERIMENTAL DEVELOPMENT
  • NAICS Code:
    • 541714 - Research and Development in Biotechnology (except Nanobiotechnology)
  • Place of Performance:
    Washington , DC 20024
    USA
Description

UPDATE: Question and Answers attached in documents. Date for submission revised to July 2, 2026.



The Office of Biomedical Advanced Research and Development Authority (BARDA), within the Administration for Strategic Preparedness and Response (ASPR) at the U.S. Department of Health and Human Services (HHS) seeks to use the Rapid Response Partnership Vehicle (RRPV) Consortium, an enterprise partnership in collaboration with industry and academia to facilitate research and development activities as follows:



The purpose of this RPP is to advance investigational BDBV vaccine candidates leveraging the VSV vaccine platform, which has demonstrated single dose protection in past EBOV outbreaks.



Work includes manufacturing process development through production of initial current Good Manufacturing Practice (cGMP) Phase 1 clinical trial material (CTM), with a goal of up to 10,000 doses. Early regulatory engagement will inform the critical-path IND-enabling nonclinical. The proposed approach must describe how any available platform efficiencies from prior or ongoing platform development and manufacturing to accelerate the path towards cGMP CTM production and IND submission under the U.S. FDA. Additional activities include a Phase 1 safety and immunogenicity trial as well as options for production of up to 100,000 doses of cGMP CTM.



The end goal of this effort is (1) to produce cGMP CTM and meet regulatory requirements to enable use of investigational candidate(s) in a clinical trial for the ongoing 2026 BDBV outbreak and (2) to identify successful BDBV vaccine candidates for potential further development.



Please see the attachments for more information.



Questions are due June 16, 2026 by 12 p.m. Eastern. Proposals are due by June 26 at 3 p.m. Eastern.



Submission link: https://www.rrpv.org/solicitation/bundibugyo-virus-outbreak-response-vaccines-bundivx/


Attachments/Links
Contact Information View Changes
Contracting Office Address
  • O’NEILL HOUSE OFFICE BUILDING
  • WASHINGTON , DC 20515
  • USA
Primary Point of Contact
Secondary Point of Contact
History
Commodity Codes
  • FSC AResearch and development
  • NAICS 541714Research and Development in Biotechnology (except Nanobiotechnology)
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