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Contact Activation Pathway Function Blocking Antibody AB023
Contact and place of performance
Andy Shortall
DWG, TX 78234
USA
Request for Information Notice HT9426-26-RFI-WS03 for Contact Activation Pathway Function Blocking Antibody AB023 This is a REQUEST FOR INFORMATION (RFI) ANNOUNCEMENT ONLY. It is neither a solicitation announcement nor a request for proposals or quotes and does not obligate the Government to award a contract. Requests for a solicitation will not receive a response. Responses to this RFI must be in writing. The purpos...
View moreThe Government is not obligated to, nor will it, pay for or reimburse any costs associated with responding to this RFI. This notice shall not be construed as a commitment by the Government to issue a solicitation or ultimately award a contract, nor does it restrict the Government to a particular acquisition approach. The Government will in no way be bound to this information if any solicitation is issued. No subcontracting opportunity is anticipated. The North American Classification System (NAICS) code for this acquisition is 541714 – Research and Development in Biotechnology (except Nanobiotechnology); (Small Business Size Standard 1,000 employees).
Notice to potential offerors: All offerors who provide goods or services to the United States Federal Government must be registered in the System for Award Management (SAM) at www.sam.gov and complete online representations and certification in SAM.
All interested parties shall submit information by email to: [email protected], and [email protected] to be received no later than 18 June 2026, at 10:00ET.
The Defense Health Agency (DHA) Contracting Activity is conducting market research through Sources Sought notice HT9426-26-RFI-WS03 to identify qualified offerors capable of providing the contact activation pathway function blocking antibody AB023. This requirement is classified under NAICS 541714 Research and Development in Biotechnology (except Nanobiotechnology) and PSC 6505 DRUGS AND BIOLOGICALS. The primary objective is to acquire Coagulation Factor XI (FXI) Inhibitor AB023, also known as Xisomab 3G3 or Gruticibart, for use in Extracorporeal Membrane Oxygenation (ECMO) circuits, hemodialysis, catheters, and cancer-related thrombosis. Responses are due by June 18, 2026, and the designated place of performance is DWG, Texas.
The required antibody must bind to the "apple 2" domain of FXI to inhibit activation by activated factor XII (FXIIa) in the contact pathway while preserving natural hemostasis. Specific performance criteria include providing a maximum of 0.5g of AB023 annually and conducting pharmacokinetics and pharmacodynamics testing to analyze the biochemical, physiological, and molecular effects of the drug. The product must effectively prevent platelet-rich thrombus growth and fibrin accumulation in vascular thrombosis models, causing a dose-dependent prolongation of activated partial thromboplastin time without affecting Prothrombin Time. Technical expertise must be validated through clotting assays to ensure the stability, dose, and potency of the antibody.
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