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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 businessHigher educationGovernmentNonprofitForeign 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.