Bli medlem
Bli medlem

Du är här


Oasmia Pharmaceutical AB Provides Updates to Clinical Program Development

des Updates to Clinical Program Development

OASM advances global commercialization efforts for all products

New York, 2016-02-24 08:30 CET (GLOBE NEWSWIRE) --

New York, February 24, 2016 ? Oasmia Pharmaceutical AB (Nasdaq: OASM), a
developer of a new generation of drugs within human and veterinary oncology,
today announced updates on the clinical development of its family of products
that it has continued to advance and commercialize in countries around the

-- Paclical?/Apealea?. Last month, Oasmia announced that Paclical had been
submitted for marketing authorization to the European Medicines Agency
(EMA). Oasmia anticipates Overall Survival Data for this product,
alternatively branded Apealea by the Company for use in Europe, during the
second quarter of 2016 that it will add to the existing submission to EMA.
The data resulting from this study will also be used as the basis for the
Company?s US submission to FDA. Discussions of label extension are ongoing
and as a part of that, a dose-finding study of weekly administration in
metastatic breast cancer patients has been completed and the results are
currently under evaluation.

-- Docecal?. The investigators? meeting for the safety and tolerance study
with Docecal, the Company?s next generation anti-cancer drug, was held as
planned on December 11, 2015. Investigators and study nurses from the
clinics participated and were given a presentation of the study as well as
its design and procedures. The First Patient In study is planned for the
first quarter of 2016 with a Phase I crossover pharmacokinetic study
comparing Docecal to Taxotere commencing in the second quarter of 2016.

-- Doxophos?/Doxophos Vet?.Oasmia submitted application for market approval in
Russia and CIS in December 2015. For other markets, the company has planned
a Phase I study with Doxophos, but has decided to await safety data
resulting from its ongoing study in dogs. The dogs so far evaluated have
not shown any signs of heart problems, often considered a common side
effect of treatment using doxorubicin.

-- Paccal Vet?. As Oasmia recently regained its global distribution rights
from Zoetis, it has revised its treatment strategy for Paccal Vet. The
Company has planned to change the product from a specialized treatment for
a small group of veterinary oncologists, to a product that can be used in a
large number of veterinary clinics. One step towards this goal is to
introduce a lower dose which has less severe side effects and appeal to a
broader market. The evaluation of the Phase III study in dogs with mast
cell tumors will begin shortly, and its results will most likely play a
factor on how the indication will be utilized moving forward.

?It is extremely encouraging to see the Oasmia portfolio of human and animal
oncology treatments continue to move forward in terms of their development and
commercialization,? said Julian Aleksov, Executive Chairman of Oasmia. ?These
treatments, built upon our patented XR17 technology, represent what we believe
to be immediate and future solutions for how physicians and patients address
various forms of cancer. As we develop and execute sales for these products, we
are confident in the Company?s long-term position among industry leaders.?

Notes to editors:

About the Apealea/Paclitaxel Market
The two leading paclitaxel-based products on the market are Taxol and
Abraxane?, two widely used cancer drugs. Taxol indications are breast cancer,
non-small cell lung cancer, pancreatic cancer, ovarian cancer and AIDS-related
Kaposis sarcoma. Taxol generated $1.6 billion in sales in 2000 alone, prior to
losing its patent protection in 2001. In 2013, Taxol generated $92 million in
post-patent sales. Abraxane, which received FDA approval in 2005 for metastatic
breast cancer, followed by approvals for lung non-small cell lung cancer (in
2012) and metastatic pancreatic cancer (in 2013), generated $759 million in
worldwide annual sales in 2013 and $979 million in 2014.

About Apealea
Apealea is a Cremophor-free formulation of the well-known cytostatic paclitaxel
combined with Oasmia?s excipient technology XR17. Paclitaxel is one of the most
widely used anticancer substances and is included in the standard treatment of
a variety of cancers such as lung cancer, breast cancer and ovarian cancer.
Apealea consists of a freeze-dried powder, which is dissolved in conventional
solutions for infusion. It has orphan drug designation in the EU and the US.

About epithelial ovarian cancer
In 2012, 239,000 women were diagnosed with ovarian cancer globally. Epithelial
ovarian cancers account for about 85% to 90% of ovarian cancers, and are the
most aggressive and dangerous sub-type. In the EU, the five-year survival rate
for ovarian cancer was 37.6% from 2000-2007 according to a study published in
The Lancet. In 2012, there were 44,149 diagnosed cases of ovarian cancer in the
EU, according to the European Cancer Observatory/International Agency for
Research on Cancer; 29,758 of these women died of ovarian cancer. Common
chemotherapy drugs used for the treatment for ovarian cancer include cisplatin
or carboplatin, and paclitaxel or docetaxel, which are most often given in

About Oasmia Pharmaceutical AB
Oasmia Pharmaceutical AB develops new generations of drugs in the field of
human and veterinary oncology. The company?s product development aims to create
and manufacture novel nanoparticle formulations and drug-delivery systems based
on well-established cytostatics which, in comparison with current alternatives,
show improved properties, reduced side-effects, and expanded applications. The
company?s product development is based on its proprietary in-house research and
company patents. Oasmia is listed on NASDAQ USA (OASM.US), Frankfurt Stock
Exchange (OMAX.GR, ISIN SE0000722365) and NASDAQ Stockholm (OASM.ST).

Oasmia Pharmaceutical AB Forward Looking Statements
This announcement contains forward-looking statements. These statements are
based on expectations in light of the information that is currently available,
as well as assumptions that are subject to risks and uncertainties that could
cause actual results to differ materially from such statements. These risks and
uncertainties include, but are not limited to, domestic and international
economic conditions, industry and market conditions, and changes of interest
rate and currency exchange rate, in general, and completion and discontinuation
of clinical trials, obtaining regulatory approvals, claims and concerns about
product safety and efficacy, technological advances, domestic and foreign
healthcare reforms, and changes of laws and regulations, in particular, with
respect to each of Paclical. The company disclaims any intention or obligation
to update or revise any forward-looking statements whether as a result of new
information, future events or otherwise. This announcement contains information
on pharmaceuticals (including pharmaceuticals under development) but is not
intended to, and does not, make any representations, warranties or claims
regarding the efficacy or effectiveness of these pharmaceuticals or provide
medical advice of any kind.

Apealea and Paclical are registered trademarks of Oasmia Pharmaceutical.
Cremophor is a registered trademark of BASF. Abraxane is a registered trademark
of Celgene. Taxol is a registered trademark of Bristol-Myers Squibb.

When ?Taxol? is used in this press release, it refers to Taxol as well as to
generic formulations of Taxol.

For more information, please contact:
Margareta Eriksson, Vice President Clinical Development
Tel: +46 18 50 54 40

For media relations:
Eric Fischgrund
Tel: +1 (646) 699 1414

Författare SSE

Tala om vad ni tycker

Tala om vad ni tycker

Ni är just nu inne på en betaversion av nya aktiespararna. Lämna gärna feedback på vad ni tycker i formuläret nedan.