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NIH funding notice PAR-21-124

Innovation Grants to Nurture Initial Translational Efforts (IGNITE): Assay Development and Neurotherapeutic Agent Identification (R61/R33 Clinical Trial Not Allowed)

Closed on October 21, 2024.

Posted
March 11, 2021
Close date
October 21, 2024
Activity codes
R61, R33
Institutes taking part
NINDS, NCCIH

Read the notice on Grants.gov · NIH Guide page

The notices it replaced

  1. Reissues: PAR-18-762 Innovation Grants to Nurture Initial Translational Efforts (IGNITE): Assay Development and Neurotherapeutic Agent Identification (R61/R33 Clinical Trial Not Allowed)
  2. 2 steps back: PAR-15-070 Innovation Grants to Nurture Initial Translational Efforts (IGNITE): Assay Development and Therapeutic Agent Identification and Characterization to Support Therapeutic Discovery (R21/R33)

Replaced by PAR-25-059.

Who won it before

34 competing awards (new and renewals) from FY2014 to FY2025 under this notice and the notices it replaced: $13,132,796 in first-year total cost, median $391,745.

Most frequent study sections

  1. Neurological Sciences and Disorders B Study Section[NSD-B]18
  2. Neurological Sciences and Disorders A Study Section[NSD-A]15
  3. Neurological Sciences and Disorders C Study Section[NSD-C]1

Most frequent institutions

  1. DUKE UNIVERSITY2
  2. JOHNS HOPKINS UNIVERSITY2
  3. MASSACHUSETTS GENERAL HOSPITAL2
  4. MAYO CLINIC ROCHESTER2
  5. SCRIPPS FLORIDA2
Competing awards under PAR-21-124 and the notices it replaced
FYProjectPIsInstitutionFirst-year costStudy section
2025Development of therapeutics for SCA481R61NS138384-01A1SCAGLIONE, KENNETH MATTHEWDUKE UNIVERSITY, NC$392,863NSD
2025Optimized Anti-Epileptic Screening Using Drosophila Models1R61NS134960-01A1REITER, LAWRENCE TTULANE UNIVERSITY OF LOUISIANA, LA$363,602NSD
2025High-throughput small molecule screen to reduce endogenous level of Msh3 for disease-modifying HD therapy1R61NS140733-01YANG, XIANGDONG WILLIAMUNIVERSITY OF CALIFORNIA LOS ANGELES, CA$345,114NSD
2024OPC-X screen: Discovery of small molecule inhibitors to overcome extrinsic inhibition of remyelination.1R61NS133257-01A1AKASSOGLOU, KATERINAJ. DAVID GLADSTONE INSTITUTES, CA$458,325NSD
2024Development and validation of a high throughput screening assay for identification of tau aggregation inhibitors in Alzheimer's disease1R61NS136666-01SOTO, CLAUDIOUNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON, TX$371,919NSD
2024Screening for Nuclear Receptor TLX ligands1R61NS133955-01A1BURRIS, THOMAS PUNIVERSITY OF FLORIDA, FL$323,079NSD
2023Development of a phenotypic screening assay for novel compounds that inhibit peripheral pain-sensing neurons1R61AT012117-01A1CLARKE, WILLIAM PUNIVERSITY OF TEXAS HLTH SCIENCE CENTER, TX$437,991NSD
2023In vivo SELEX strategies to identify potent aptamer-drug conjugates for glioblastoma1R61NS128071-01A1MAHER, LOUIS JAMESSARKARIA, JANN N.MAYO CLINIC ROCHESTER, MN$414,690NSD
2023Engineered tissue arrays to streamline deimmunized DMD gene therapy vectors1R61NS133080-01ODOM, GUY LEARYUNIVERSITY OF WASHINGTON, WA$411,074NSD
2023High content analgesic screening from human nociceptors1R61AT011938-01A1DUSSOR, GREGORY OKOLBER, BENEDICT JPANCRAZIO, JOSEPH J.UNIVERSITY OF TEXAS DALLAS, TX$370,187NSD
2023Identification of botanical hHv1 channel blockers as analgesics for neuropathic pain1R61AT012544-01GOLDSTEIN, STEVE A NZHAO, RUIMINGUNIVERSITY OF CALIFORNIA-IRVINE, CA$256,401NSD
2022Optimizing Small Molecule Read-Through Compounds for Treating AtaxiaTelangiectasia1R61NS119708-01A1MATHEWS, PAUL JAMESLUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER, CA$508,727NSD
2022Identifying compounds that target APOE4 associated brain endothelial dysfunction1R61NS124970-01 · under PAR-18-762TAI, LEON MAINGUNIVERSITY OF ILLINOIS AT CHICAGO, IL$358,909NSD
2022Drug Discovery for First-In-Class Myosin 10 Inhibitors as a Novel Target for Glioblastoma1R61NS121386-01A1 · under PAR-18-762KAMENECKA, THEODORE MMILLER, COURTNEY ARUMBAUGH, GAVIN RSCAMPAVIA, LOUIS DANIELSPICER, TIMOTHY PATRICKSWEENEY, H LEESCRIPPS FLORIDA, FL$185,371NSD
2021Deve inlopment of A High-Throughput Screen for Identification of Targeted Therapies in Brainstem Tumors with the H3K27M Mutation1R61NS114147-01A1 · under PAR-18-762DANIELS, DAVIDMAYO CLINIC ROCHESTER, MN$899,750NSD
2021High throughput screen for discovery of N-acetyltransferase 8 Like (NAT8L) inhibitors1R61NS119659-01 · under PAR-18-762SLUSHER, BARBARA STAUCHTSUKAMOTO, TAKASHIJOHNS HOPKINS UNIVERSITY, MD$409,354NSD
2021Employing functionalized fragment libraries to identify therapeutic agents for neurofibromatosis type 21R61NS119658-01 · under PAR-18-762KISSIL, JOSEPHSCRIPPS FLORIDA, FL$57,529NSD
2020HTS to identify compounds that increase NAD+ levels in neurons and muscle cells1R61NS111375-01A1 · under PAR-18-762BAUR, JOSEPH A.HURYN, DONNA MKHURANA, TEJVIR SUNIVERSITY OF PENNSYLVANIA, PA$575,548NSD
2020Screening for DNA damage response modulators in glioblastoma stem cells1R61NS117554-01 · under PAR-18-762BADR, CHRISTIAN ELIASTANNOUS, BAKHOS AMASSACHUSETTS GENERAL HOSPITAL, MA$420,000NSD
2020Development of cellular HTS for 20S proteasome enhancers1R61NS111347-01A1 · under PAR-18-762LISABETH, ERIKA MATHESNEUBIG, RICHARD RTEPE, JETZE J.MICHIGAN STATE UNIVERSITY, MI$355,857NSD
2019High-throughput Screen for Discovery of Ciliary Neurotrophic Factor (CNTF) Receptor Agonists for the Treatment of Amyotrophic Lateral Sclerosis (ALS)1R61NS110960-01 · under PAR-18-762ROSSOLL, WILFRIEDMAYO CLINIC JACKSONVILLE, FL$453,500NSD
2019GALV-Based Retroviral Replicating Vectors for Glioma Gene Therapy1R21NS104454-01A1 · under PAR-15-070KASAHARA, NORIYUKIUNIVERSITY OF CALIFORNIA, SAN FRANCISCO, CA$401,456NSD
2019Non-opioids for inflammatory pain: Adenylyl cyclase 1 as a novel target1R61NS111070-01 · under PAR-18-762ROMAN, DAVID L.WATTS, VAL JUNIVERSITY OF IOWA, IA$400,720NSD
2019Drug discovery for spinocerebellar ataxia, using novel fluorescence technology targeting β-III-spectrin1R61NS111075-01 · under PAR-18-762HAYS, THOMAS SUNIVERSITY OF MINNESOTA, MN$383,926NSD
2019Slack Potassium Channel Inhibitors for the Treatment of Childhood Epilepsies1R21NS109521-01 · under PAR-15-070EMMITTE, KYLE AWEAVER, C DAVIDVANDERBILT UNIVERSITY, TN$290,733NSD
2018Immortalized Striatal Precursor Neurons as a Screenable Model of HD1R21NS104320-01A1 · under PAR-15-070ROSS, CHRISTOPHER AJOHNS HOPKINS UNIVERSITY, MD$403,537NSD
2018High-content screening for modulators of lamin B1 as a therapeutic target in autosomal dominant leukodystrophy1R21NS106087-01 · under PAR-15-070PADIATH, QUASAR SVOGT, ANDREASUNIVERSITY OF PITTSBURGH AT PITTSBURGH, PA$390,626NSD
2018Small molecule stabilizers of Hsp70 for treatment of spinal and bulbar muscular atrophy1R21NS101030-01A1 · under PAR-15-070LIEBERMAN, ANDREW POSAWA, YOICHIUNIVERSITY OF MICHIGAN AT ANN ARBOR, MI$388,542NSD
2018Development of SK channel modulators as therapeutic agents for ataxia1R21NS101182-01A1 · under PAR-15-070BEZPROZVANNY, ILYA BZHANG, MIAOCHAPMAN UNIVERSITY, CA$186,750NSD
2017Developing Novel RNA-Based Therapeutics for Parkinson's Disease1R21NS096032-01A1 · under PAR-15-070DISNEY, MATTHEW DMOURADIAN, M. MARALRBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL, NJ$452,438NSD
2017Anticonvulsant screening using chronic epilepsy models1R21NS096948-01A1 · under PAR-15-070BERDICHEVSKY, YEVGENYDUDEK, F. EDWARDDULLA, CHRIS GSTALEY, KEVIN J.MASSACHUSETTS GENERAL HOSPITAL, MA$443,878NSD
2017Discovery of Post-transcriptional utrophin upregulator small molecules for Duchenne Muscular Dystrophy therapeutics1R21NS102838-01 · under PAR-15-070KHURANA, TEJVIR SUNIVERSITY OF PENNSYLVANIA, PA$402,500NSD
2017Allele-specific RNA-targeted lead compounds for Huntington's disease1R21NS099516-01A1 · under PAR-15-070WARNER, KATHERINE DEIGANRIBOMETRIX, LLC, NC$260,150NSD
2016Inhibitors of TrkB Signaling1R21NS094863-01 · under PAR-15-070MCNAMARA, JAMES O.DUKE UNIVERSITY, NC$357,750NSD

Data: Grants.gov's daily extract and NIH's notice pages and award files, in ScienceGraph release conductgrants-2026-11-09-0.1.0. An award is listed only where NIH's own record names the notice, and a PI only by NIH's profile ID. Grants.gov and NIH do not endorse ScienceDex.

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PAR-21-124: Innovation Grants to Nurture Initial Translational Efforts (IGNITE): Assay Development and Neurotherapeutic Agent Identification (R61/R33 Clinical Trial Not Allowed) | ScienceDex | ConductScience