Improved Performance of the DiLA2 siRNA Delivery Platform With Proprietary Peptide NanoparticlesBOTHELL, WA, Jun 08, 2009 (MARKETWIRE via COMTEX) -- MDRNA, Inc. (NASDAQ: MRNA) announced today in vivo data from a
bladder cancer model demonstrating effective localized delivery of a
UsiRNA to a solid tumor, thus further expanding the delivery
capabilities of the DiLA2 Platform. In addition, the Company reported
in vivo data demonstrating the ability of its proprietary
peptide-based nanoparticle technology to significantly improve siRNA
delivery efficiency. The integration of the peptide nanoparticle
technology with the DiLA2 Platform resulted in 85% knockdown of ApoB
messenger RNA while decreasing the overall amount of the DiLA2
delivery vehicle by 45%. The data are being presented today at the
RNA Interference Summit in San Francisco by Roger Adami, Ph.D.,
Associate Director, Molecular Pharmaceutics, MDRNA, Inc.
Dr. Adami will also present data demonstrating knockdown of
additional hepatocyte targets in rodent models. The DiLA2 liposomes
showed 90% knockdown of DGAT2 in mice following a single 2 mg/kg
administration and a 75% knockdown of PCSK9 with a single 2 mg/kg
dose. This highly efficient delivery to hepatocytes provides the
basis for MDRNA's development pipeline in oncology.
"The data reported today demonstrate the breadth and versatility of
the DiLA2 delivery system," stated Barry Polisky, Ph.D., Chief
Scientific Officer. "We believe that the DiLA2 Platform will enable
effective therapeutic applications of siRNAs in oncology and various
other disease indications. Additionally, peptide-siRNA particles
combined with the DiLA2 Platform will provide improved delivery
efficiency of RNAi-based therapeutics. During 2009, we intend to
expand the capabilities of the DiLA2 delivery system to target
multiple oncology indications beyond our initial internal program in
liver cancer."
About UsiRNAs
UsiRNAs are duplex siRNAs that are modified with non-nucleotide
acyclic monomers, termed unlocked nucleobase analogs (UNA), in which
the bond between two adjacent carbon atoms of ribose is removed.
UsiRNAs are fully recognized by the RNAi machinery and provide for
potent RNAi activity. Placement of UNA within a UsiRNA minimizes the
potential for off-target effects by the guide strand as well as
undesired activity of the passenger strand. Further, the change in
sugar structure renders this unlocked nucleobase analog
conformationally flexible. The flexibility of the monomer escapes the
body's surveillance mechanisms associated with cytokine induction, as
well as providing protection from nuclease degradation.
About the DiLA2 Platform
The DiLA2 Platform is MDRNA's proprietary platform for creating novel
liposomal delivery systems from amino acids. The platform enables
MDRNA to tailor the charge, linker and acyl chains of amino acids in
order to optimize the liposome for delivery to the target tissue of
interest and is designed to permit attachment of various peptides and
other targeting molecules to improve a variety of delivery
characteristics. In addition, MDRNA is utilizing peptides for
nanoparticle formulations to increase cellular uptake and endosomal
release.
About MDRNA, Inc.
MDRNA is a biotechnology company focused on the development and
commercialization of therapeutic products based on RNA interference
(RNAi). Our goal is to improve human health by combining novel
RNAi-based compounds and proprietary peptide- and liposomal-based
drug delivery technologies to provide superior therapeutic options.
Our multi-disciplinary portfolio of capabilities includes molecular
biology, cellular biology, formulation expertise, peptide and
alkylated amino acid chemistry, pharmacology, toxicology and
bioinformatics. We are applying this expertise to a single,
integrated drug discovery platform that will be the engine for our
clinical pipeline and a versatile platform for establishing broad
therapeutic partnerships. We are also building on new technologies,
such as UsiRNAs that incorporate the non-nucleotide moiety Unlocked
Nucleobase Analog (UNA) within the siRNA molecule, that we expect to
lead to safer and more effective RNAi-based therapeutics. By
combining broad expertise in siRNA science with proven delivery
platforms and a strong and growing IP position, MDRNA is well
positioned as a leading RNAi therapeutics company and value-added
collaborator for our research partners. Additional information about
MDRNA, Inc. is available at http://www.mdrnainc.com.
Forward-Looking Statement
Statements made in this news release may be forward-looking
statements within the meaning of Federal Securities laws that are
subject to certain risks and uncertainties and involve factors that
may cause actual results to differ materially from those projected or
suggested. Factors that could cause actual results to differ
materially from those in forward-looking statements include, but are
not limited to: (i) the ability of MDRNA to obtain additional
funding; (ii) the ability of MDRNA to attract and/or maintain
manufacturing, research, development and commercialization partners;
(iii) the ability of MDRNA and/or a partner to successfully complete
product research and development, including preclinical and clinical
studies and commercialization; (iv) the ability of MDRNA and/or a
partner to obtain required governmental approvals; and (v) the
ability of MDRNA and/or a partner to develop and commercialize
products that can compete favorably with those of competitors.
Additional factors that could cause actual results to differ
materially from those projected or suggested in any forward-looking
statements are contained in MDRNA's most recent periodic reports on
Form 10-K and Form 10-Q that are filed with the Securities and
Exchange Commission. MDRNA assumes no obligation to update and
supplement forward-looking statements because of subsequent events.
Contacts:
Matthew D. Haines
Senior Director, Investor Relations and Corporate Communications
(212) 209-3874
Email Contact
McKinney|Chicago (Media)
Alan Zachary
(312) 944-6784 x 316 or
(708) 707-6834
Email Contact
SOURCE: MDRNA, Inc.
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