AJ13--Pharmarcokinetics for Experimental Rheumatoid Arthritis treatment
Veterans Affairs, Department of · VETERANS AFFAIRS, DEPARTMENT OF
Opportunity details
AJ13--Pharmarcokinetics for Experimental Rheumatoid Arthritis treatment is currently listed as accepting responses on SAM.gov. Buyer context: Veterans Affairs, Department of · VETERANS AFFAIRS, DEPARTMENT OF. Industry classification: All Other Animal Production (NAICS 112990). Product/service classification: GENERAL SCIENCE & TECHNOLOGY R&D SVCS; GENERAL SCIENCE & TECHNOLOGY; EXPERIMENTAL DEVELOPMENT (PSC AJ13). Performance location: USA. Notice type: Sources Sought. GovGazette adds public award history and related pages to help you decide whether to keep reading. Check all requirements on SAM.gov.
- Check the NAICS and PSC codes, set-aside rules, place of performance, and time left before the deadline.
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- Response deadline
- Jul 31, 2026, 9:00 AM EDT
- Set-aside
- None listed
- Place of performance
- USA
- Posted
- Jul 16, 2026
- Solicitation
- 36C24526Q0669
- PSC
- GENERAL SCIENCE & TECHNOLOGY R&D SVCS; GENERAL SCIENCE & TECHNOLOGY; EXPERIMENTAL DEVELOPMENTAJ13
- Contracting office
- 245-NETWORK CONTRACT OFFICE 5 (36C245) · LINTHICUM · MD
- Source
- SAM.gov
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: [email protected] 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.
What similar awards have paid
See what agencies paid for similar work. This public history does not set a bid price, estimate a cost, or predict an award.
Typical award size
$81,000
Middle of the pack for similar past awards
Most similar awards fall between $46,600 and $156,900
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Drawn from official USAspending contract records. Always confirm requirements on the SAM.gov notice before you bid.
For research only. This is not legal advice or a promise of an award. Always verify requirements on the official SAM.gov notice. Past award amounts are public history, not a suggested bid or prediction. Open the original SAM.gov notice for the official record.