A02. Sources Sought Notice - Celltheon Antibody.pdf
PDF 144 KB Posted
- Solicitation number
- PANMRA-24-P-0000-0044333
- Issued by
-
Defense Health Agency
About this file
This document is a Sources Sought Notice issued by the U.S. Army Medical Research Acquisition Activity (USAMRAA) on behalf of the U.S. Army Medical Research Institute of Chemical Defense (USAMRICD). The notice is seeking market research to identify parties interested in and capable of providing anti-carfentanil monoclonal antibody (mAb) for use in non-human primate research.
The key requirements include providing over 4 grams of anti-carfentanil mAb in phosphate buffered saline at a concentration over 75 mg/mL, aliquoted into 5-20 mL vials. The mAb must be generated using Celltheon's Chinese hamster ovary (CHO) cell line, be safe for use in non-human primates, and be delivered to USAMRICD no later than June 1, 2025. The anticipated contract type is firm-fixed price. Responses are due by July 12, 2024. The requirement may be set aside for small businesses or procured through full and open competition. Respondents must provide details on their capabilities, past relevant experience, and ability to meet the set-aside requirements if applicable.
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INTRODUCTION:
The U.S. Army Medical Research Acquisition Activity (USAMRAA) is issuing this sources sought notice (SSN) on behalf of the U.S. Army Medical Research Institute of Chemical Defense (USAMRICD) as a means of conducting market research to identify parties having an interest in and the resources to support the requirement for Anti- Carfentanil monoclonal antibody (mAb) for use in Non-Human Primates.
Based on the responses to this sources sought notice, this requirement may be set-aside for small business (in full or in part) or procured through full and open competition. All small business set-aside categories will be considered. Telephone inquiries will not be accepted or acknowledged, and no feedback or evaluations will be provided to companies regarding their submissions.
PLACE OF PERFORMANCE:
All work contained in this requirement shall be performed at the contractor’s or subcontractor’s facility.
DISCLAIMER:
This is a Request for Information (RFI), as defined in FAR 15.201(e), to ascertain available capabilities for planning purposes.
This RFI is issued solely for information and planning purposes and does not constitute a solicitation. Neither unsolicited proposals nor any other kind of offers will be considered in response to this RFI. Responses to this notice are not offers and will not be accepted by the Government to form a binding contract. In keeping with the standards of FAR Part 10, the Government may request additional information from responders. Responders are solely responsible for all expenses associated with responding to this RFI or any follow-up information request. All information received in response to this RFI or any follow-up information request that is marked Proprietary will be handled accordingly. Responses to the RFI will not be returned. At this time, questions concerning the composition and requirements for a future request for proposal will not be entertained.
PROGRAM BACKGROUND:
The USAMRICD requires anti-carfentanil mAb to complete research milestones in support of an National Institute of Health (NIH) Interagency Agreement (IAA) in collaboration with the University of Washington. Work on small animals has already been completed by Dr. Pravetoni at the University of Washington, and his lab utilizing anti-fentanyl mAbs procured from Celltheon. Due to the proprietary nature of the Celltheon cells used in prior work, further work can only be done using mAbs from Celltheon due to its protein expressions and hybridoma technology.
MINIMUM ESSENTIAL CHARACTERISTICS (MECs):
• >4 grams of anti-carfentanil mAb in phosphate buffered saline (pH 7.4) at a concentration of >75 mg/mL
• Aliquoted aseptically into 5-20 mL vials sealed with septa.
• Generated via Celltheon’s Chinese hamster ovary (CHO) cell line
• Safe for use in non-human primates (such as African green monkeys)
• Data package sent to USAMRICD containing viability, viable cell density, productivity trends, specific productivity, and titer prior to the stable pool generation and prior to purification.
• Delivery to the USAMRICD no later than 01 June 2025
CAPABILITY:
If your organization has the potential capacity to provide the required supplies, please provide the following information: 1) Organization name, address, email address, Web site address, telephone number, and size and type of ownership for the organization; and 2) a tailored capability statement addressing the particulars of this effort, with appropriate documentation supporting claims of organizational and staff capability. If significant subcontracting or teaming is anticipated in order to deliver technical capability, organizations should address the administrative and management structure of such arrangements.
ELIGIBILITY:
• The North American Industry Classification System (NAICS) for this acquisition is 541714, Research and Development in Biotechnology (except Nanobiotechnology).
• The Product Service Code is 6509, Drugs and Biologicals, veterinary use.
• Each respondent must clearly identify their business size/status in their capabilities statement.
THIS DOCUMENTATION MUST ADDRESS AT A MINIMUM THE FOLLOWING ITEMS:
1) What type of work has your company performed in the past in support of the same or similar requirement?
2) Can or has your company managed a task of this nature? If so, please provide details.
3) Can or has your company managed a team of subcontractors before (if subcontractors would be needed)? If so, provide details.
4) What specific technical skills does your company possess which ensure capability to perform the tasks?
5) For small businesses, please note that under a Small-Business Set-Aside, in accordance with FAR 52.219-14, the small business prime must perform at least 50% of the work themselves in terms of the cost of performance.
Provide an explanation of your company’s ability to perform at least 50% of the tasks.
6) Provide a statement including current small/large business status and company profile to include number of employees, annual revenue history, office locations, SAM Unique Entity ID, etc.
7) Include in your response your ability to meet the requirements in the Facility and Safeguarding requirements.
ADDITIONAL INFORMATION AND SUBMISSION DETAILS (CAPABILITIES STATEMENT)
Interested parties are requested to submit a capabilities statement of no more than three (3) pages in length in Times New Roman font of not less than 10 pitch. The deadline for response to this request is no later than 4:00 PM, Eastern Time, 12 July 2024. All responses under this Sources Sought Notice must be submitted to the Contract Specialist at benjamin.t.marcus2.civ@health.mil.
1) The Delivery to the USAMRICD no later than 01 June 2025
2) The contract type is anticipated to be Firm Fixed Price.
3) Responses to this Sources Sought, including any capabilities statement, shall be electronically submitted in either Microsoft Word or Portable Document Format (PDF).
4) All data received in response to this Sources Sought that is marked or designated as corporate or proprietary will be fully protected from any release outside the Government.
5) All questions must be submitted to the Contract Specialist at benjamin.t.marcus2.civ@health.mil. Questions submitted by email/phone call will not be monitored. The Government is not committed nor obligated to pay for the information provided, and no basis for claims against the Government shall arise as a result of a response to this Sources Sought. No phone calls will be accepted.
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