AJ13--Pharmarcokinetics for Experimental Rheumatoid Arthritis treatment
Closed Pre-Solicitation Posted
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- Solicitation number
- 36C24526Q0669
- Agency
-
Veterans Integrated Service Network 5
Veterans Health Administration, Department of Veterans Affairs
- Responses due
- Set-aside
- No set-aside
Opportunity facts
- NAICS code
- 112990 All Other Animal Production
- PSC
- AJ13 General Science & Technology R&D Svcs; General Science & Technology; Experimental Development
- Place of performance
- Contractors Lab/Facility See notice for details 21218, United States
- Points of contact
Notice details come from SAM.gov. Updated .
About this opportunity
The Department of Veterans Affairs Veterans Integrated Service Network 5 is conducting market research for preclinical toxicology and pharmacokinetic studies on an experimental rheumatoid arthritis treatment, with capability statements due July 31, 2026. This sources sought notice is not a solicitation and does not commit the Government to award a contract.
The VA seeks qualified vendors to perform GLP-compliant toxicity testing and GLP or non-GLP pharmacokinetic studies in adult rats on peptide-displaying liposomes containing 150 mg dexamethasone with 80% encapsulation efficiency. Toxicity studies require single-dose intravenous testing in 20–32 rats (male and female) with clinical observations, weight and food intake tracking over 14 days, blood testing for organ damage markers, and histopathology of major organs. Pharmacokinetic studies involve administering single IV doses to 12–24 rats (balanced sexes), collecting blood samples at 8–10 defined time points over 48 hours, and performing LC-MS/MS quantification of dexamethasone and its metabolite 6-hydroxydexamethasone to generate PK parameters.
Work will be performed under GLP for toxicity studies; PK studies may be conducted under GLP or non-GLP conditions. The anticipated period of performance runs September 15, 2026, through September 14, 2027. Responses must include demonstrated experience with GLP toxicology, rodent pharmacokinetic studies, LC-MS/MS analysis, and histopathology. The VA encourages responses from small businesses, SDVOSBs, VOSBs, 8(a) firms, HUBZone businesses, and WOSBs. Selected vendors will be required to execute a Confidential Disclosure Agreement before receiving proprietary information. Submit responses to Contracting Officer Robert O'Keefe Jr. at robert.okeefejr@va.gov.
Notice text
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.
Files
| File | Type | Posted |
|---|---|---|
| 36C24526Q0669.docx | DOCX document |
Notice history
| Notice | Type | Posted |
|---|---|---|
| AJ13--Pharmarcokinetics for Experimental Rheumatoid Arthritis treatment | Pre-Solicitation | |
| This notice | Pre-Solicitation |
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