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OpenU01Clinical trial: Optional / allowed

Translational Efforts to Advance Gene-based Therapies for Ultra-Rare Neurological and Neuromuscular Disorders (U01 - Clinical Trial Optional)

National Institutes of Health (NIH) · NIH Institute/Center · PAR-25-327

Source: Grants.gov · View original posting ↗

Award
Amount not listed
Deadline
Oct 8, 2027
Letter of intent
Mechanism
U01
Duration
Expected awards
Funding cycle
Standard NIH dates
Open date
Dec 18, 2024
Total funding
Clinical trial
Optional / allowed
Established investigatorSmall businessGovernmentHigher educationNonprofitForeign entities

Research areas

Therapeutics & drug discoveryClinical trials

Auto-classified from the title and description (keyword-based) — may be imperfect.

Description

The Ultra-Rare Gene-Based Therapy (URGenT) network supports Investigational New Drug (IND)-enabling studies and planning activities for First-in-Human (FIH) clinical testing of gene-based or transcript-directed therapeutics, such as oligonucleotides and viral-based gene therapies, for ultra-rare neurological or neuromuscular disorders. The goal of this announcement is to accelerate the development of a promising clinical candidate with robust biological rationale and demonstrated proof of concept (POC) data for the intended approach in a model system relevant to a specified patient population towards an IND filing and the initiation of a clinical trial.

Data notes: award amount not published in the source feed; administering NIH institute could not be identified from the opportunity number.