AJ13--Pharmarcokinetics for Experimental Rheumatoid Arthritis treatment

Location: Federal
Posted: Jul 16, 2026
Due: Jul 31, 2026
Agency: VETERANS AFFAIRS, DEPARTMENT OF
Type of Government: Federal
Category:
  • A - Research and development
Solicitation No: 36C24526Q0669
Publication URL: To access bid details, please log in.
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AJ13--Pharmarcokinetics for Experimental Rheumatoid Arthritis treatment
Active
Contract Opportunity
Notice ID
36C24526Q0669
Related Notice
Department/Ind. Agency
VETERANS AFFAIRS, DEPARTMENT OF
Sub-tier
VETERANS AFFAIRS, DEPARTMENT OF
Office
245-NETWORK CONTRACT OFFICE 5 (36C245)
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General Information
  • Contract Opportunity Type: Sources Sought (Original)
  • Original Published Date: Jul 16, 2026 07:27 am EDT
  • Original Response Date: Jul 31, 2026 09:00 am EDT
  • Inactive Policy: Manual
  • Original Inactive Date: Sep 29, 2026
  • Initiative:
    • None
Classification
  • Original Set Aside:
  • Product Service Code: AJ13 - GENERAL SCIENCE & TECHNOLOGY R&D SVCS; GENERAL SCIENCE & TECHNOLOGY; EXPERIMENTAL DEVELOPMENT
  • NAICS Code:
    • 112990 - All Other Animal Production
  • Place of Performance:
    Contractors Lab/Facility See notice for details , 21218
    USA
Description
SOURCES SOUGHT NOTICE

Department of Veterans Affairs
Network Contracting Office (NCO) 05
Title: A Joint Targeted Drug Delivery Approach for Arthritis Therapy Toxicity and Pharmacokinetics

1. Purpose
This Sources Sought Notice is issued solely for market research in accordance with FAR Part 10. This is not a solicitation, and it does not commit the Government to issue a solicitation or make an award. The Department of Veterans Affairs (VA) seeks to identify qualified vendors capable of performing preclinical toxicology and pharmacokinetic (PK) studies on an experimental Rheumatoid Arthritis treatment involving peptide-displaying liposomes containing dexamethasone.

2. Requirement Overview
The VA requires a contractor to perform GLP-compliant toxicity testing and GLP or non GLP pharmacokinetic studies in adult rats. These studies support advancement toward a future FDA Pre IND meeting for the patented joint-targeted liposomal delivery system developed under prior VA-funded research.

3. Summary of Required Services

A. Toxicity Studies (GLP Required)
Receive peptide displaying liposomes containing 150 mg dexamethasone, 80% encapsulation efficiency, with Certificate of Analysis.
Conduct single dose intravenous toxicity testing in 20 32 rats (male and female).
Record clinical observations, weight, and food intake over a 14 day period.
Conduct blood testing for organ damage markers (liver, kidney, heart, muscle, etc.).
Perform euthanasia, necropsy, and histopathology of major organs.

B. Pharmacokinetic (PK) Studies (GLP or non GLP)
Administer single IV doses to 12 24 rats (balanced sexes).
Observe and weigh animals before and after dosing.
Collect blood samples at 8 10 defined time points (10 min through 48 hours).
Process plasma and store at 20°C.
Perform chemical extraction and LC MS/MS quantification of dexamethasone and metabolite 6 hydroxydexamethasone (6OHDEX).
Generate PK parameters (t½, Cmax, AUC, etc.).

C. Final Deliverable
Comprehensive written report summarizing toxicity, PK parameters, and analytical results.

4. Place of Performance
Vendor s laboratory.
Toxicology tasks must be performed under GLP.
PK tasks may be performed under GLP or non GLP.

5. Period of Performance 1 year of service (if necessary)
September 15, 2026 September 14, 2027.

6. Requested Information from Interested Vendors

Please submit the following in your capability statement:

Company name, address, point of contact, phone, and email.
Unique Entity Identifier (UEI) and confirmation of active SAM.gov registration.
Business size and socio economic status under NAICS 325412.
Demonstrated technical capability and experience performing:
GLP toxicology studies
Rodent PK studies
LC MS/MS analysis
Histopathology and necropsy

Relevant past performance for biomedical R&D or FDA preclinical support.
Any additional information proving capability to meet the requirements.

7. Socio Economic Categories of Interest

The VA encourages responses from:
SDVOSB, VOSB, 8(a), HUBZone, WOSB, Small businesses, Large businesses

8. Point of Contact for Responses
Contracting Officer: Robert O Keefe Jr.
Email: robert.okeefejr@va.gov

Please submit all capability statements directly to the Contracting Officer for review no later than (NLT) July 29, 2026 0900 Eastern Standard Time.

Your email subject line should read:
Response to Sources Sought Notice Approach for Arthritis Therapy Toxicity and Pharmacokinetics
(NAICS 325412 / PSC AJ13)

9. Disclaimer

Upon completion of Market Research, a Confidential Disclosure Agreement (CDA) will be required of selected vendors. The CDA must be fully executed before any proprietary information is released. Selected vendors will receive exclusive access to solicitation materials and proprietary documents once the CDA is completed.

This Sources Sought Notice is for market research purposes only. Information received will assist the Government in shaping the acquisition strategy. This notice does not constitute a solicitation, does not request quotes, and does not obligate the Government to issue a solicitation or award a contract.
Attachments/Links
Contact Information
Contracting Office Address
  • 8849 International Drive Suite 215
  • LINTHICUM , MD 21090
  • USA
Primary Point of Contact
Secondary Point of Contact


History

Related Document

Jul 16, 2026[Presolicitation (Original)] AJ13--Pharmarcokinetics for Experimental Rheumatoid Arthritis treatment
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