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Preclinical Vaccine Efficacy Report and Data Package

Active

Federal

Response Deadline08/24/2026, 06:00:00 PM UTC

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

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This subcontract, titled Preclinical Vaccine Efficacy Report and Data Package, is issued by the NIH NCI under the Department of Health and Human Services. The primary objective is the compilation of a final technical report that summarizes critical data regarding vector design, production, and validation. This comprehensive documentation must include specific details on gene expression, titers, and preliminary results concerning immunogenicity or efficacy. The project is associated with NAICS code 541690 and is designated for performance in Oxford, UK. Interested parties must adhere to a tight timeline, with the opportunity posted on August 17, 2026, and a response deadline set for August 24, 2026.

General Info

NIH NCI subcontract for preclinical vaccine efficacy reporting and data package in Oxford, UK.

Agency

Department Of Health And Human Services → NIH NciView Agency

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

Oxford, GB-OXF, OX3 7DQ, GBR

Set-Aside

NONE

Documents

This scope was carved out of 75N98026Q00996.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

Sole Source - Production of ChAdOx-1 and MVA expressing mouse gp70

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Timeline

PostedAug 17

subcontract

Response DeadlineAug 24

Submission deadline

Response Deadline

08/24/2026, 06:00:00 PM UTCin 6 days

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → NIH Nci

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Health And Human Services → NIH Nci

View Agency Profile

Office AddressN/A

ContactsNo contact information available

Full Description

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Compile a final technical report summarizing vector design, production, and validation data, including gene expression, titers, and preliminary immunogenicity or efficacy results.

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