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Targeted nanoparticle gene therapy for lung cancer

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1U43CA165462-01A1
Agency Tracking Number: U43CA165462
Amount: $190,353.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: NCI
Solicitation Number: PAR10-286
Timeline
Solicitation Year: 2013
Award Year: 2013
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
900 S. Capital of Texas Hwy Suite 150
Austin, TX 78746
United States
DUNS: 801937272
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 TANELI JOUHIKAINEN
 (512) 632-7537
 tj@savarapharma.com
Business Contact
 TANELI JOUHIKAINEN
Phone: (512) 632-7537
Email: tj@savarapharma.com
Research Institution
 Stub
Abstract

DESCRIPTION (provided by applicant): Project Summary A transformational NanoNucleic delivery technology is being investigated by Savara Inc. as a promising first-in-class gene therapy candidate for lung cancer. A potent lung cancer therapy with fewer sideeffects is urgently needed due to the exceptionally high rates of morbidity and mortality of this particular cancer. Gene therapy, while promising, remains clinically unsuccessful, mainly due to insufficient therapeutic gene expression in cancer tissues, and adverse effects of the delivery vectors. Recently, a novel nanoparticle technology for nucleic acid delivery ( NanoNucleic technology) was developed at the University of Kansas, and licensed exclusively to Savara Inc, a drug development company specializing in the treatment of lung diseases. The NanoNucleic technology comprises a cationic peptide bundled with DNA (or RNA for siRNA delivery), and condensed by calcium into small nanoparticles (75-100 nm). Using the NanoNucleic technology, high local expression of endogenous apoptosis inducer genes (TRAIL and angiotensin II type 2 receptor (AT2R)) was achieved in the lungs of mice. Over-expression of either gene induced marked cell death in several human lung cancer cell lines in culture, but the effect onnormal lung epithelial cells or fibroblasts was minimal. AT2R over-expression also induced significant cell death in lung cancer progenitor cells in culture. After administering an intratracheal spray o AT2R or TRAIL genes as NanoNucleic formulations to LLC mice, gene expression lasted at least two weeks. Observations of the treated lungs revealed a remarkable reduction in tumor burden, without any signs of toxicity toward the native tissue, nor signs of inflammation. Unlike viral vector-based gene therapy,NanoNucleic gene therapy is expected to generate minimal host immune response and none of the viral gene- associated drawbacks such as gene mutations or the production of oncogenes via random insertion into the genome. The aim of the proposed research isto provide therapeutic proof-of- concept of an optimized form of NanoNucleic gene therapy approach using two different therapeutic gene candidates (AT2R, and TRAIL) in two different in vivo lung cancer models. NanoNucleic formulations will be administeredintratracheally, with or without complementary intravenous administration. The strong preliminary data in the mouse LLC model suggest a high likelihood of success in this proposed Phase I research. Successful completion of the Phase I will enable advancement of the program into efficacy studies using K-ras gene mutation- and tobacco carcinogen-induced lung cancer models, as well as chronic safety studies in larger animals, and thereby build a solid foundation for eventual translational research. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: Project Narrative The primary objective of this research is to develop a practical gene therapy for non-small cell lung cancer by developing a nanoparticle gene-delivery system. Treatment strategy proposed here is significantly better than existing therapeutic strategies since efficient therapeutic outcomes with fewer side effects are expected.

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

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