Novagali Pharma Announces Enrollment of the First Patients in a Pivotal Phase III Study of Cyclokat® for Dry Eye Disease
April 05 2011 - 2:00AM
Business Wire
Regulatory News:
Novagali Pharma (Paris:NOVA), a pharmaceutical company that
develops innovative ophthalmic products, today announced enrollment
of the first patients in Sansika study, the European multi-national
confirmatory pivotal Phase III study of Cyclokat® in patients with
severe Dry Eye Disease. The Company received a positive Scientific
Advice from the European Medicines Agency (EMA) regarding the final
steps in the development of Cyclokat® last December.
Cyclokat® is a cyclosporine ophthalmic formulation intended for
the treatment of patients suffering from severe Dry Eye Disease.
Cyclokat® is a proprietary cationic emulsion employing the
Novasorb® technology that optimizes the absorption of cyclosporine
in tissues of the eye surface which makes once-a-day dosing
possible.
The Sansika® study is a multicenter, randomized, double-masked,
two parallel arms, vehicle-controlled, 6 month phase III trial of
Cyclokat® in patients with severe Dry Eye Disease with a 6 month
open label treatment safety follow-up period. Approximately 250
patients will be enrolled across 6 European Union member states.
This pivotal phase III clinical trial follows two phase II studies
performed in Europe and in the US and, the Siccanove study, the
first European phase III study of Cyclokat® conducted in patients
with moderate to severe Dry Eye Disease.
Ronald R. Buggage, M.D., Chief Scientific Officer of Novagali
Pharma, states: “Dry eye disease is a bilateral chronic
inflammatory disease of the ocular surface characterized by
inflammation and symptoms of ocular discomfort resulting from an
inadequate quantity or quality of tears. In severe cases, there is
damage to the cornea (keratitis) as a result of the on-going ocular
surface inflammation that can lead to an increased risk of
infection, vision loss and impaired quality of life. In patients
with severe DED there is an urgent need for a safe and effective
anti-inflammatory therapy.”
Jérôme Martinez, Chief Executive Officer of Novagali Pharma,
concludes: “No effective treatment for dry eye disease is currently
marketed in Europe, leaving a major unsatisfied medical need in 18
million patients1. Cyclokat® could be the first product approved in
Europe for this indication and in view of this market opportunity
we choose to focus our efforts on developing our product in this
market. This Phase III clinical trial of Cyclokat® is intended to
support the Marketing Authorisation Application that we expect to
file in the last quarter of 2012. This major milestone in the final
clinical development phase of Cyclokat® substantially improves its
medical value and attractiveness.”
About NOVAGALI Pharma
(www.novagali.com)
Founded in 2000, Novagali Pharma SA is a pharmaceutical company
that develops ophthalmic innovative products for all segments of
the eye. Thanks to its three proprietary technology platforms, the
Company has an advanced portfolio of highly innovative products,
one of which is already on sale and two of which are undergoing
phase III clinical trials.
In 2009, Frost & Sullivan recognised Novagali with the Award
for Industry Innovation & Advancement of the Year, for its
proprietary emulsion technology platforms, and Siemens awarded the
company the “Health Award” Grand Prix de l’Innovation for
Novasorb®.
In April 2010, Novagali Pharma and its partners in the Vitrena
project obtained €9.4 million in funding from Oséo for this
diabetic retinopathy project. Novagali Pharma carried out a
successful IPO in July 2010 enabling the Company to raise €22
million.
1 Prevalence of Dry Eye for Top 5 EU countries - Datamonitor
2010
Next press release:2010 annual
results on April 26, 2011(after market)
Novagali Pharma is listed on NYSE Euronext
Paris - Compartment CISIN code: FR0010915553 - Ticker: NOVA
This press release contains certain forward-looking statements.
Although the company believes its expectations are based on
reasonable assumptions, these forward-looking statements are
subject to numerous risks and uncertainties, which could cause
actual results to differ materially from those anticipated. For a
discussion of risks and uncertainties which could cause the
company’s actual results, financial condition, performance or
achievements to differ from those contained in the forward-looking
statements, please refer to the Risk Factors (“Facteurs de Risques
») section of the Document de Base filed with the AMF, which is
available on the AMF website (http://www.amf-france.org) or on
Novagali Pharma’s website (www.novagali.com). This press release
and the information contained herein do not constitute an offer to
sell or a solicitation of an offer to buy or subscribe to
securities of Novagali Pharma in any country.
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