NanoViricides Inc : NanoViricides to Present at the 14th Annual BIO-CEO Conference in NYC today
02/13/2012| 07:05am US/Eastern

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NanoViricides, Inc. (OTC BB: NNVC)
(the "Company") announced today that its President, Dr. Anil Diwan, will
present an overview of the company at the 14th
Annual BIO CEO and Investor Conference. The Conference is being held
at the Waldorf-Astoria Hotel in New York City (http://www.bio.org/events/conferences/14th-annual-bio-ceo-investor-conference).
NanoViricides, Inc. presentation is scheduled for 1pm today, February
13th.
NanoViricides, Inc., is developing a broad range of anti-viral
therapeutics against a number of different viruses. This is enabled by
its novel nanoviricides® platform technology. A nanoviricide is designed
to look like the cell surface to the virus, complete with the "landing
sites" that the virus seeks on the cell surface to bind to the cell and
thereafter enter the cell. These "landing sites" are designed into the
nanoviricide by chemically incorporating "ligands" to which the virus is
expected to bind. The Company strives to develop ligands that closely
mimic the native landing sites of the virus. Even as a virus mutates
constantly, these landing sites to which the virus binds remain the
same. The Company therefore believes that its drugs would be effective
against a large range of strains and mutations of a given virus.
The Company has recently declared a clinical drug candidate against
influenza in its FluCide? program, namely, NV-INF-1. The Company has
also requested a pre-IND Meeting with the US FDA to discuss the
development plan for NV-INF-1.
In addition, the Company has developed drug candidates against HIV,
Dengue, and Adenoviral Epidemic Kerato-Conjunctivitis (EKC) that have
all shown extremely high efficacies in pre-clinical animal studies. The
Company has also developed drug candidates against Herpes that have
shown strong efficacies in pre-clinical studies. These additional four
commercially important programs are at pre-clinical candidate
optimization stage. The Company has several R&D programs against many
other viruses including Ebola/Marburg and Rabies viruses.
The Company thus has an extremely broad drug pipeline, enabled by its
novel, first-in-class, platform technology.
The Company is planning on two separate indications for NV-INF-1: High
strength dosage form for hospitalized patients with severe influenza,
and a single course therapy for the out-patients with less severe
influenza.
In the USA alone, there are approximately 300,000 severe influenza cases
that require hospitalization every year resulting in approximately
40,000 deaths. Expert physician advice suggests that the dosage form
should be a high strength solution suitable for "piggy-back"
incorporation into the standard IV fluid supplement system that is
commonly used in hospitalized patients. Since current influenza
treatments have limited effectiveness in these patients because of the
severity of the infection and the stage of progression, there is a
significant unmet medical need for the treatment of hospitalized
influenza patients, which include immunocompromised patients.
NV-INF-1 promises to be a highly effective anti-influenza drug, based on
the extremely high efficacy observed in animal studies, and the Company
believes that it would receive rapid and widespread acceptance for the
treatment of hospitalized patients with severe influenza.
The Company is planning the out-patient treatment as a single injection
that a medical office can easily administer when the patient goes for
the first clinical visit. The Company believes that in most instances no
follow-on treatment would be necessary. This expectation is based on the
following results from its animal studies: (1) the extremely high
treatment effectiveness in inhibiting the cycle of infection, virus
expansion and spread of infection and, (2) the significantly long
lasting effects of the drug treatment after the drug is discontinued.
A single course treatment for out-patients is a highly sought after goal
in influenza therapeutics. During the 2009 H1N1 "swine flu" pandemic,
approximately 61 million cases of out-patient influenza were estimated
in the USA alone.
The Company's anti-influenza clinical drug candidate is expected to be
effective against a majority of strains and types of influenzas
including novel epidemic influenza strains such as the one encountered
in 2009-2010 (so called "swine flu"); seasonal flu such as H1N1, H3N2;
highly pathogenic types such as H7N and H9N; as well as the highly
lethal type, so called "bird flu" or H5N1. All influenza viruses use the
same common receptor to bind to human cells. Therefore the Company
believes that its influenza drug candidate should work against most of
the influenza viruses.
The market size for anti-influenza drugs is currently estimated to be
approximately $4-$7 billion worldwide. The Company believes that if its
FluCide? drug becomes available, the influenza drug market size could
expand substantially. The market size for OTC medications for control of
influenza symptoms is approximately $2.1 billion dollars annually in the
USA, and about £0.6 billion (about $1 billion) in the UK (source: http://www.mintel.com/press-centre/press-releases/410/consumers-cough-up-for-remedies-as-flu-season-starts-early).
Similar large market sizes are reported for other countries across the
globe.
The Company has previously reported on the extremely high efficacies of
its optimized FluCide? drug candidates. The Company is now advancing one
of the tested optimized FluCide candidates as the clinical drug
candidate after performing substantial further analysis.
About
NanoViricides:
NanoViricides,
Inc. (www.nanoviricides.com)
is a development stage company that is creating special purpose
nanomaterials for viral therapy. The Company's novel nanoviricide® class
of drug candidates are designed to specifically attack enveloped virus
particles and to dismantle them. The Company is developing drugs against
a number of viral diseases including H1N1 swine flu, H5N1 bird flu,
seasonal Influenza, HIV, oral and genital Herpes, viral diseases of the
eye including EKC and herpes keratitis, Hepatitis C, Rabies, Dengue
fever, and Ebola virus, among others.
This press release contains forward-looking statements that reflect the
Company's current expectation regarding future events. Actual events
could differ materially and substantially from those projected herein
and depend on a number of factors. Certain statements in this release,
and other written or oral statements made by NanoViricides, Inc. are
"forward-looking statements" within the meaning of Section 27A of the
Securities Act of 1933 and Section 21E of the Securities Exchange Act of
1934. You should not place undue reliance on forward-looking statements
since they involve known and unknown risks, uncertainties and other
factors which are, in some cases, beyond the Company's control and which
could, and likely will, materially affect actual results, levels of
activity, performance or achievements. The Company assumes no obligation
to publicly update or revise these forward-looking statements for any
reason, or to update the reasons actual results could differ materially
from those anticipated in these forward-looking statements, even if new
information becomes available in the future. Important factors that
could cause actual results to differ materially from the company's
expectations include, but are not limited to, those factors that are
disclosed under the heading "Risk Factors" and elsewhere in documents
filed by the company from time to time with the United States Securities
and Exchange Commission and other regulatory authorities. Although it is
not possible to predict or identify all such factors, they may include
the following: demonstration and proof of principle in pre-clinical
trials that a nanoviricide is safe and effective; successful development
of our product candidates; our ability to seek and obtain regulatory
approvals, including with respect to the indications we are seeking; the
successful commercialization of our product candidates; and market
acceptance of our products.

NanoViricides, Inc.
Amanda Schuon, 310-550-7200
info@nanoviricides.com
© Business Wire 2012
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