Minor Use Minor Species Development of Drugs (R01)
An FDA R01 funding safety and effectiveness testing to support approval of drugs for minor uses or minor species (MUMS) in veterinary medicine. Eligibility is limited to entities developing such dr…
- Deadline
- Jan 29, 2027
- Posted
- May 29, 2024
- Award amount
- Up to $250,000
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We’ll email you before Jan 29, 2027 so you have time to apply.
In plain English
An FDA R01 funding safety and effectiveness testing to support approval of drugs for minor uses or minor species (MUMS) in veterinary medicine. Eligibility is limited to entities developing such drugs (or their research partners) that already hold an INAD file and a MUMS designation from FDA/CVM, with a protocol pre-reviewed by FDA, so this requires existing regulatory standing with FDA. Awards reach up to about $250,000. Not a fit unless the applicant is already in the FDA veterinary drug development pipeline.
AI-generated summary to help you decide quickly — verify the official eligibility rules before applying.
Who can apply
• Faith-based or Community-based Organizations• Regional Organizations• Non-domestic (non-U.S.) Entities (Foreign Organizations)
About this grant
This Notice of Funding Opportunity (NOFO) is issued by the Food and Drug Administration (FDA), Center for Veterinary Medicine (CVM), and solicits Research Project (R01) grant applications from institutions or organizations that propose to develop or support the development of designated new animal drugs intended for minor uses in major species or for use in minor species (MUMS). The FDA is authorized to provide grants to assist in defraying the costs of qualified safety and effectiveness testing that could be used to satisfy the requirements for FDA approval of MUMS-designated drugs. Only entities developing drugs for veterinary use or parties working as research partners with such entities are eligible for grants. The organization (or applicant) seeking approval of the new animal drug under investigation must have opened an Investigational New Animal Drug (INAD) file with FDA/CVM and must hold a minor use or minor species "designation" granted by FDA/CVM's Office of Minor Use and Minor Species Animal Drug Development (OMUMS) for that drug for a specified intended use, in accordance with the provisions of section 573 of the Food, Drug and Cosmetic Act (21 U.S.C. 360ccc-2) and 21 CFR part 516. FDA/CVM's Office of New Animal Drug Evaluation (ONADE) must have reviewed and concurred with the proposed study protocol before an applicant can submit a grant application.
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Source: public records via Grants.gov. UseGrants is an independent aggregator, not affiliated with any funding agency. Always confirm details on the official listing before applying.