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Closed

Hereditary Hemorrhagic Telangiectasia (HHT) Center

Posted
June 8, 2026
Closes
July 10, 2026
Award ceiling
$2,900,000
Program funding
$2,900,000
Expected awards
1
Cost sharing
No
Instrument
Cooperative Agreement
Assistance listing
93.110
Category
Health
Archives
August 30, 2026

Program funding history

Awards made under Assistance Listing 93.110 across FY2024–FY2026, from public federal spending records.

FY2024 obligated
$271M
FY2025 obligated
$258.3M
FY2026 (to date) obligated
$69.3M
Awards in window
887

Top recipients: Zero To Three National Center for Infants, Toddlers & Families, University Hospitals Cleveland Medical Center, Children's National Medical Center, Michigan Public Health Institute, American Academy of Pediatrics

Source: USAspending.gov · refreshed August 2026

This opportunity is closed. Applications are no longer accepted. Similar open grants are listed below, and the free Tuesday digest carries the next ones like it.

Synopsis

The purpose of the Hereditary Hemorrhagic Telangiectasia (HHT) Center Program is to reduce illness and death related to HHT by partnering with clinical center to expand access and coordination of care; creating innovative strategies that support clinicians with identifying and diagnosing HHT cases; and developing a de-identified, aggregate patient data registry to better understand this rare disease and its treatment outcomes.

Who can apply

"Domestic" means the 50 states, the District of Columbia, the Commonwealth of Puerto Rico, the Northern Mariana Islands, American Samoa, Guam, the U.S. Virgin Islands, the Federated States of Micronesia, the Republic of the Marshall Islands, and the Republic of Palau.

How to apply

Applications go through the official government listing. Grants Radar links you straight to the source — applying is free.

View on Grants.gov

Agency contact: Health Resources and Services Administration · [email protected] · 301-443-7432

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