Gennao Bio Presents New Data on Novel Gene Monoclonal Antibody Platform Technology at the American Association for Cancer Research (AACR) 2021 Annual Meeting

~ Preclinical data show the utility of Gennao’s proprietary first-in-class monoclonal antibody 3E10-D31N (GMAB^D31N), a cell penetrating antibody, to non-covalently bind to and systemically deliver therapeutic levels of multiple types of nucleic acid payloads to cells in vitro and tumors in vivo ~

~ GMAB^D31N combined with a RIG-I ligand 3pRNA (GMAB^D31N/3pRNA) efficiently targets and delivers a known RIG-I agonist to tumors in vivo and effectively prevents tumor growth in a mouse model of melanoma, comparable to anti-CTLA-4 ~

NEW HAVEN, Conn., April 10, 2021 (GLOBE NEWSWIRE) — Gennao Bio, a privately-held genetic medicines company developing first-in-class, targeted nucleic acid therapeutics, today announced a late-breaking poster detailing preclinical results for its proprietary, non-viral gene monoclonal antibody (GMAB) nucleic acid delivery system. The data were presented at the American Association for Cancer Research (AACR) Annual Meeting 2021.

The GMAB technology platform, exclusively licensed from Yale University, utilizes a proprietary, cell-penetrating antibody to non-covalently bind to and deliver therapeutic levels of multiple types of nucleic acids, including synthetic RNA (ribonucleic acid) messenger RNA, small interfering RNA, deoxyribonucleic acids, antisense oligonucleotides and gene editing molecules.

The preclinical data presented in the poster show the utility of the monoclonal antibody 3E10-D31N (GMAB^D31N) to deliver nucleic acids to cells in vitro and to tumors in vivo. This antibody, a modified version of 3E10, forms non-covalent complexes with RNAs and can mediate highly specific delivery broadly into tumors via intravenous injection by targeting the nucleoside transporter ENT2. ENT2 is highly expressed in multiple tumor types as well as skeletal and cardiac muscle.

Studies completed with labeled RNAs and messenger RNAs expressing a green fluorescent protein reporter gene show tumor specific delivery and functional expression by imaging, with minimal delivery to healthy tissues. Cell culture studies show antibody-mediated delivery of a series of retinoic acid-inducible gene I (RIG-I) ligands, including hairpin RNAs and synthetic double-stranded RNA (poly(I:C)), resulting in robust RIG-I stimulation and induction of type-1 interferon signaling. Most importantly, when using a mouse B16 melanoma tumor model, substantial tumor growth suppression was observed upon intravenous injection of GMAB^D31N non-covalently bound to 3pRNA, an 89-nucleotide, single-stranded RNA. In this study, the tumor suppression observed was comparable to the tumor suppression that was observed using anti-CTLA-4.

“The preclinical results presented today highlight the ability of GMAB^D31N to systemically deliver immunostimulatory RNAs in a targeted, non-invasive manner,” said Peter M. Glazer, M.D., Ph.D., Chair of the Department of Therapeutic Radiology, Professor of Genetics and Robert E. Hunter Professor of Therapeutic Radiology at the Yale School of Medicine. “This approach has the potential to offer new and significant treatment advantages over current delivery methods that are associated with systemic toxicity or rely on direct intra-tumoral injection, which is therapeutically sub-optimal, especially for metastatic disease. I look forward to working with Gennao Bio on the continued development of the GMAB platform to develop effective therapeutics for the treatment of oncology indications, as well as monogenic skeletal and cardiac muscle diseases.”

The full abstract and poster presentation can be accessed on the AACR annual meeting website, www.aacr.org, through June 21, 2021.

About Gennao Bio

Gennao Bio is a privately-held genetic medicines company developing first-in-class targeted nucleic acid therapeutics utilizing its proprietary gene monoclonal antibody (GMAB) platform technology. GMAB technology utilizes a novel, cell-penetrating antibody to non-covalently bind to and deliver therapeutic levels of a wide variety of nucleic acid payloads to select cells. This non-viral delivery platform offers significant advantages over traditional gene delivery systems as it can deliver multiple types of nucleic acids, allows for repeat dosing and dose optimization, and can be easily and affordably manufactured. Gennao Bio is developing this delivery system with an initial focus on oncology and monogenic skeletal muscle diseases.

Investor and Media Contact:

Gennao Bio
Chris Duke
732-735-0330
cduke@gennaobio.com

Source: Gennao Bio