Inyx Inc · 8-K · For 6/16/04 · EX-99.1
Filed On 6/29/04 12:26pm ET · SEC File 333-83152 · Accession Number 1010549-4-413
As Of Filer Filing As/For/On Docs:Pgs Issuer Agent
6/29/04 Inyx Inc 8-K{5,7} 6/16/04 3:36 Securities Tran..Corp/FA
Current Report · Form 8-K
Filing Table of Contents
Document/Exhibit Description Pages Size
1: 8-K Current Report 2 10K
2: EX-10.24 Supply Agreement Dated June 11, 2004 32 119K
3: EX-99.1 Press Release Dated June 29, 2004 2 13K
EX-99.1 · Press Release Dated June 29, 2004
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Exhibit 99.1
PRESS RELEASE - FOR IMMEDIATE RELEASE
INYX SELECTED BY ASTRAZENECA
TO DEVELOP AND PRODUCE NON-OZONE-DEPLETING
HFA-`PULMICORT' ASTHMA SPRAY FOR EUROPEAN MARKETS
- Initial Multi-Year, Contract Valued At Over $6.5 Million Annually to Inyx
NEW YORK - June 29, 2004 - Inyx, Inc. (OTC BB: IYXI), an emerging specialty
pharmaceutical company with a focus on niche drug delivery technologies and
products, announced today that it has been awarded a multi-year contract by
AstraZeneca AB, a major international healthcare company, to assist in the
development and production of a non-ozone depleting hydrofluoralkane (HFA)
version of AstraZeneca's Pulmicort asthma spray for European markets.
Based on an initial three and a half-year contract, which has extension options,
Inyx's wholly owned United Kingdom subsidiary, INyX Pharma Limited, will
immediately commence development and commercialization work on AstraZeneca's
HFA-version of Pulmicort, one of the world's leading asthma medicines. The
contract is valued at over $6.5 million annually to Inyx, based on present sales
of the chlorofluorocarbon (CFC) version of Pulmicort. Subject to regulatory
approval in European markets, commercial production is planned to commence in
the first quarter of 2005.
Pulmicort is an inhaled anti-inflammatory glucocorticosteroid (budesonide),
primarily for once- or twice-daily maintenance treatment of asthma. Pulmicort is
also indicated for the treatment of chronic obstructive pulmonary disease in
some countries. The World Health Organization estimates that approximately 100
million people worldwide suffer from asthma, and that chronic obstructive
pulmonary disease is the fourth greatest cause of death worldwide. Currently,
Pulmicort utilizes CFC as an aerosol gas propellant, which is an ozone-depleting
agent. The European Union has implemented a ban on ozone-depleting agents such
as CFC in pharmaceutical products.
Dr. Jack Kachkar, Chairman and President of Inyx, said, "We are extremely
gratified to have been selected by AstraZeneca for their HFA-Pulmicort program
in Europe. This contract reflects Inyx's expertise in converting CFC aerosol
pharmaceuticals to HFA drug delivery products, as we have already conducted such
conversion for other clients in Europe and Canada.
"The selection by AstraZeneca," he added, "is a significant milestone event for
Inyx."
AstraZeneca is a major international healthcare business engaged in the
research, development, manufacture and marketing of prescription pharmaceuticals
and the supply of healthcare services. It is one of the world's leading
pharmaceutical companies with healthcare sales of over $18.8 billion and leading
positions in sales of gastrointestinal, oncology, cardiovascular, neuroscience
and respiratory products. The company currently employs over 11,600 people at 11
R&D centres in seven countries, including the U.K., Sweden, the U.S., Canada,
France, India and Japan.
About Inyx
Inyx, Inc. is an emerging specialty pharmaceutical company with niche aerosol
drug delivery technologies and products. Inyx focuses its expertise on contract
manufacturing of prescription and over-the-counter pharmaceutical products, and
provides specialty pharmaceutical development and production consulting services
to the international healthcare market. In addition, Inyx is developing its own
proprietary products to be marketed by selected clients and strategic partners.
The company's operations are conducted through its wholly owned subsidiary, INyX
Pharma Limited, with a focus on niche products and technologies for the
treatment of respiratory, allergy, dermatological and topical conditions. INyX
Pharma's client base comprises large ethical pharmaceutical corporations,
branded generic companies and biotechnology firms. The company develops and
manufactures for a majority of global markets, including: North America, Europe,
Latin America and the Middle East. INyX Pharma's R&D and production facilities
are in Runcorn, near Manchester, England. Another wholly owned subsidiary, Inyx
Canada, Inc. based in Toronto, provides business development and support
services. Inyx, Inc.'s corporate offices are in New York City.
Safe Harbor
Statements about the Company's future expectations, including future revenues
and earnings, and all other statements in this press release other than
historical facts, are "forward-looking statements" within the meaning of Section
27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of
1934, and as that term is defined in the Private Securities Litigation Reform
Act of 1995. The Company intends that such forward-looking statements be subject
to the safe harbors created thereby. Since these statements involve risks and
uncertainties and are subject to change at any time, the Company's actual
results could differ materially from expected results.
For more information, please contact:
Jay M. Green, Executive Vice President
Dates Referenced Herein and Documents Incorporated By Reference
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| For The Period Ended | | 6/16/04 |
| Filed On / Filed As Of | | 6/29/04 | | 1 |
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