e6vk
Form 6-K
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Report of Foreign Private Issuer
Pursuant to Rules 13a-16 or 15d-16 of
the Securities Exchange Act of 1934
Dated: October 25th, 2006
ALTANA Aktiengesellschaft
(Translation of Registrants name into English)
Am Pilgerrain 15
D-61352 Bad Homburg v. d. Höhe
Federal Republic of Germany
(Address of principal executive offices)
Indicate by check mark whether the Registrant files or will file annual reports under cover Form
20-F or Form 40-F.
Form 20-F þ Form 40-F o
Indicate by check mark if the Registrant is submitting the Form 6-K in paper as permitted by
Regulation S-T Rule 101(b)(1):
Indicate by check mark if the Registrant is submitting the Form 6-K in paper as permitted by
Regulation S-T Rule 101(b)(7):
Indicate by check mark whether the Registrant by furnishing the information contained in this Form
is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the
Securities Exchange Act of 1934.
Yes o No þ
If Yes is marked, indicate below the file number assigned to the Registrant in connection with
Rule 12g3-2(b): 82-
This Report on Form 6-K is hereby incorporated by reference into the Registrants Registration
Statements on Form S-8, dated September 13, 2002 (File No. 333-99485), dated September 24, 2003
(File No. 333-109074), dated September 24, 2004 (File No. 333-119240), and dated September 26, 2005
(File No. 333-128583).
This Report on Form 6-K contains:
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Press Release of October 23rd, 2006 |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly
caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
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ALTANA Aktiengesellschaft
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Dated: October 25th, 2006 |
By: |
/s/Hermann Küllmer
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Name: |
Dr. Hermann Küllmer |
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Title: |
Chief Financial Officer and
Member of the Management
Board |
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By: |
/s/ Rudolf Pietzke
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Name: |
Dr. Rudolf Pietzke |
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Title: |
General Counsel |
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ALTANA Pharma receives approval to market Ciclesonide Nasal Spray in the U.S.
OMNARIS to broaden Ciclesonide product platform
Bad Homburg/Konstanz, Germany, October 23, 2006 ALTANA AG (NYSE: AAA; FSE: ALT) announced today
that the U.S. Food and Drug Administration (FDA) has granted marketing approval for OMNARIS
(Ciclesonide nasal spray), 200µg once-daily.
OMNARIS is an intranasal corticosteroid containing Ciclesonide as active substance. It is
indicated for the treatment of nasal symptoms associated with seasonal and perennial allergic
rhinitis in patients 12 years of age and older. In addition, the FDA determined OMNARIS approvable
for the indication in children ages 2 to 11 years of age.
With the approval of OMNARIS we offer patients with allergic rhinitis an innovative treatment
option, said Dr. Hans-Joachim Lohrisch, Member of the Board of ALTANA AG and CEO of ALTANA Pharma.
OMNARIS will extend our Ciclesonide product platform by an important new therapeutic from ALTANA
Pharmas own research.
OMNARIS is ALTANA Pharmas first product which is subject to the new out-licensing strategy
regarding commercialization in the U.S. The market introduction of OMNARIS in the U.S. is being
planned for 2007 depending on negotiations with external partners.
Intranasal corticosteroids are considered to be the gold standard for the treatment of allergic
rhinitis, and they work by reducing inflammation the major underlying cause of nasal symptoms.
Ciclesonide: A broader product platform
Based on Ciclesonide ALTANA Pharma is developping a broader product platform. Besides the nasal
spray, Ciclesonide is also the active substance of an inhaled corticosteroid, that is already
approved in 39 countries worldwide for the treatment of persistent asthma. A new drug application
for this inhaled corticosteroid has also been filed with the U.S. FDA. A new drug submission (NDS)
for Ciclesonide nasal spray was submitted to the Canadian regulatory authority Health Canada in
January 2006. In addition, the Ciclesonide platform will also include a fixed combination product
with a long-acting beta-agonist, currently in phase II of clinical development. ALTANA Pharma
partners with Sanofi-Aventis in the United States and with Teijin in Japan on various Ciclesonide
based products.
About Allergic Rhinitis
Allergic rhinitis is a chronic inflammatory disease of the nasal mucosa causing sneezing, itching,
nasal congestion, and discharge. Seasonal allergic rhinitis is caused by substances that trigger
allergies and is sometimes referred to as hay fever. Perennial allergic rhinitis is a chronic
condition caused by triggers such as pet dander and dust. The result of poorly controlled allergies
can result in impairments in day-to-day activities as well as a reduction in a patients quality of
life. According to the American Academy of Allergy,
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Asthma, and Immunology, more than 40 million Americans are currently estimated to suffer with
allergic diseases and allergies are the sixth leading cause of chronic disease in the United
States.
This press release contains forward-looking statements, i.e., current estimates or expectations
of future events or future results. The forward-looking statements appearing in this press release
include information on the planned market introduction of OMNARIS in the U.S. These statements are
based on beliefs of ALTANAs management as well as assumptions made by and information currently
available to ALTANA. Many factors that ALTANA is unable to predict with accuracy could cause
ALTANAs actual results, performance or achievements to be materially different from those that may
be expressed or implied by such forward-looking statements. These factors include ALTANAs ability
to develop and launch new and innovative pharmaceutical products, the level of ALTANAs investment
in pharmaceuticals related R&D, decisions of the competent regulatory authorities, the sales and
marketing methods used by ALTANA to distribute its pharmaceuticals and the composition of ALTANAs
pharmaceuticals portfolio.
Forward-looking statements speak only as of the date they are made. ALTANA does not intend, and
does not assume any obligation, to update forward-looking statements to reflect facts,
circumstances or events that have occurred or changed after such statements have been made.
This press release is also available on the Internet at www.altana.com.
For inquiries please contact:
ALTANA AG
Dr. Thomas Gauly
Head of Corporate Communications &
Investor Relations
Media Relations:
P + 49 (0) 6172 1712-160
P + 49 (0) 6172 1712-150
F + 49 (0) 6172 1712-158
Investor Relations:
P + 49 (0) 6172 1712-163
P + 49 (0) 6172 1712-165
F + 49 (0) 6172 1712-158
Investor Relations USA:
P +1 212 974 61 92
F +1 212 974 61 90