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Studies Addressing Rare Neurodegenerative Diseases including ALS

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Contract Overview

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

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The Food and Drug Administration, under the Department of Health and Human Services, has issued a forecast for a funding opportunity aimed at advancing medical product development for interventions related to ALS and other rare neurodegenerative diseases in both adults and children. The primary objective of these studies is to address critical knowledge gaps and inform the development of products designed to prevent, diagnose, mitigate, treat, or cure these conditions. This opportunity is categorized under NAICS code 541715 and was posted on August 14, 2024. Interested parties can coordinate with the grantor, Terrin Brown, regarding the application process and specific study requirements to ensure the research exerts a significant impact on the treatment of rare neurodegenerative diseases.

General Info

FDA seeks research funding to advance therapies and diagnostics for ALS and rare neurodegenerative diseases in adults and children.

Agency

Department Of Health And Human Services → Food And Drug Administration

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)View NAICS

Place of Performance

Not specified

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

Posted

forecast

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → Food And Drug Administration
Contacts1 person available
OfficeUSA
Organization / Agency
Department Of Health And Human Services → Food And Drug Administration
Office AddressUSA
Contacts

Full Description

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The purpose of this funding opportunity announcement (FOA) is to support studies that advance medical product development of interventions intended to prevent, diagnose, mitigate, treat, or cure ALS and other rare neurodegenerative diseases in adults and children. Through the support of these studies, FDA expects to address critical knowledge gaps, exert a significant impact on rare neurodegenerative diseases, and to inform current or future product development.  

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