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Correction of Splicing Defects in Cystic Fibrosis with Peptide-Oligonucleotide Conjugates and Small Molecule Enhancing Compounds

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41TR002692-01
Agency Tracking Number: R41TR002692
Amount: $224,931.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: NCATS
Solicitation Number: PA18-575
Timeline
Solicitation Year: 2018
Award Year: 2019
Award Start Date (Proposal Award Date): 2019-01-15
Award End Date (Contract End Date): 2021-01-14
Small Business Information
408 LYONS RD, Chapel Hill, NC, 27514-7631
DUNS: 079581510
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 RUDOLPH JULIANO
 (919) 619-2001
 rudyatinitos@gmail.com
Business Contact
 RUDOLPH JULIANO
Phone: (919) 619-2001
Email: rudy_juliano@med.unc.edu
Research Institution
 UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
 ROOM 102 CARRINGTON HALL
CHAPEL HILL, NC, 27599
 Nonprofit college or university
Abstract
ABSTRACT The pathogenesis of Cystic FibrosisCFis caused by mutations in the gene for CFTRa cAMP activated chloride channel that regulates salt and water transport in epithelial tissuesespecially those in the airwaysRecent progress has resulted in small molecule therapeutic agents that partially correct defects in the CFTR protein due to certain mutationsHoweverin a substantial fraction of CF patients the disease is due to splicing defects in the CFTR gene that cannot be directly addressed using small molecule therapeuticsIn these patients splice switching oligonucleotidesSSOsmay provide a means to correct the underlying molecular defect and permit expression of fully functional CFTR proteinSSOs have recently enjoyed success in treating other genetic disorders in patientsincluding Duchenne muscular dystrophyDMDand spinal muscular atrophySMAhowever they have not yet been applied to CFAlthough this concept is appealingthe effective delivery of oligonucleotides remains a problem for the entire field of oligonucleotide based therapeutics and may be especially challenging in the airwaysThus we intend to use a novel dual approach to attain effective delivery of corrective SSOs to airway epithelial cellsFirst we will make use of oligonucleotides that are chemically conjugated to shortpositively charged peptides that augment cellular uptake of the oligonucleotideIn particular we will use P PMOs in which the peptidePis conjugated to an unchargednon toxic morpholinoPMOoligonucleotideSecondwe will make use of recently discovered oligonucleotide enhancing compoundsOECsi esmall molecules that release oligonucleotides from unproductive entrapment in endosomes thus potentiating their actionThe current proposal is designed to be a proof of concept for this dual delivery approach via testing of P PMOs and OECs in CF relevant cell culture and animal model systemsValidation of this concept would be a key step in developing a novel therapy for a significant cohort of CF patients and may have broader ramifications for use of oligonucleotides in other airway diseases!!PROJECT NARRATIVE Splice switching oligonucleotidesSSOshave been used to treat genetic disorders in patientsincluding Duchenne muscular dystrophy and spinal muscular atrophyhoweverthey have not been applied to cystic fibrosisCFOur goal is to enhance the delivery of SSOs to human CF patient airway cell cultures and in vivo in mice by dual use of peptide morpholino oligonucleotide conjugates and of small molecules that affect intracellular trafficking of oligonucleotidesValidation of this concept has impact in human health because it is a key step in developing a novel therapy for a significant cohort of CF patients and may have broader ramifications for use of oligonucleotides in other airway diseases

* Information listed above is at the time of submission. *

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