MNEXSPIKE COVID-19 Vaccine Rare Pediatric Disease Priority Review Voucher Approval Notice

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Notice

Notice of Approval of Product Under Voucher: Rare Pediatric Disease Priority Review Voucher; MNEXSPIKE (COVID-19 Vaccine, mRNA)

A Notice by the Food and Drug Administration on 04/16/2026

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• Document Details Published Content - Document Details Agencies Department of Health and Human Services Food and Drug Administration Agency/Docket Number Docket No. FDA-2026-N-3447 Document Citation 91 FR 20472 Document Number 2026-07371 Document Type Notice Page 20472
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Department of Health and Human Services

Food and Drug Administration

1. [Docket No. FDA-2026-N-3447]

AGENCY:

Food and Drug Administration, HHS.

ACTION:

Notice.

SUMMARY:

The Food and Drug Administration (FDA) is announcing the issuance of approval of a product redeeming a priority review voucher. The Federal Food, Drug, and Cosmetic Act (FD&C Act) authorizes FDA to award priority review vouchers to sponsors of approved rare pediatric disease product applications that meet certain criteria. FDA is required to publish notice of the issuance of priority review vouchers as well as the approval of products redeeming a priority review voucher. FDA has determined that MNEXSPIKE (COVID-19 Vaccine, mRNA), approved May 30, 2025, meets the criteria for redeeming a priority review voucher.

FOR FURTHER INFORMATION CONTACT:

Myrna Hanna, Center for Biologics Evaluation and Research, Food and Drug Administration, industry.biologics@fda.hhs.gov, 240-402-7911.

SUPPLEMENTARY INFORMATION:

FDA is announcing the approval of a product redeeming a rare pediatric disease priority review voucher. Under section 529 of the FD&C Act (21 U.S.C. 360ff), FDA will report the issuance of rare pediatric disease priority review vouchers and the approval of products for which a voucher was redeemed. FDA has determined that MNEXSPIKE (COVID-19 Vaccine, mRNA) meets the redemption criteria.

For further information about the Rare Pediatric Disease Priority Review Voucher Program and for a link to the full text of section 529 of the FD&C Act, go to https://www.fda.gov/​ForIndustry/​DevelopingProductsforRareDiseasesConditions/​RarePediatricDiseasePriorityVoucherProgram/​default.htm. For further information about MNEXSPIKE (COVID-19 Vaccine, mRNA), go to the Center for Biologics Evaluation and Research Approved Products website at https://www.fda.gov/​vaccines-blood-biologics/​center-biologics-evaluation-and-research-cber-product-approval-information.

Grace R. Graham,

Deputy Commissioner for Policy, Legislation, and International Affairs.

[FR Doc. 2026-07371 Filed 4-15-26; 8:45 am]

BILLING CODE 4164-01-P

Published Document: 2026-07371 (91 FR 20472)