throbber
VVestlaw,
`
`4/13/04 CANCERWK 19
`
`NewsRoom
`
`Page 1
`
`4/13/04 Cancer Wkly. Plus 19
`2004 WLNR 542429
`
`Copyright 2004 Cancer Weekly via Newst.com & Newstnet
`
`Cancer Weekly
`
`April 13, 2004
`
`Section: Expanded Reporting
`
`European launch of Faslodex reported
`Breast Cancer
`
`AstraZeneca announced the first European launches of its new breast cancer drug Faslodex ( fulvestrant) in Germany
`
`and Sweden, with Austria following imminently.
`
`The novel drug - an estrogen receptor antagonist with no agonist effects - is for the treatment of advanced breast cancer
`
`in postmenopausal women whose cancer has progressed on previous anti-estrogen treatments such as tamoxifen.
`
`Fulvestrant has been launched in the US. since May 2002, and more recently in Brazil in July 2003.
`
`Fulvestrant was approved for launch in the European Union (EU) on 12 March 2004, making it the first new type of
`
`hormonal treatment for estrogen receptor-positive breast cancer to be approved in the EU. since 1995. The launch of
`
`the drug in Germany, Sweden, and Austria therefore provides new hope to the thousands of women suffering from
`
`advanced disease in these countries. Further launches throughout Europe are expected during the course of this year.
`
`Commenting on the launch, professor Kurt Possinger, head of the oncology department at Humboldt University of
`
`Berlin, Germany, explains, "The availability of 'Faslodex' in these countries is very exciting as women who have
`
`progressed on prior tamoxifen therapy now have a new additional and effective treatment option which may help
`
`extend the window of endocrine therapy and delay the use of cytotoxic chemotherapies with their well-recognized and
`unwanted side-effects.
`
`In addition, unlike other endocrine therapies used in postmenopausal women, 'Faslodex' is a once-monthly injection
`
`which enables clinicians to have greater contact with their patients to review progress and free women of the worry of
`
`remembering to take a daily tablet, allowing them to focus on their life and not their illness."
`
`Breast cancer affects one in nine women at some point in their lives and although many tumors are detected early and
`
`© 2015 Thomson Reuters. No Claim to Orig. US Gov. Works.
`
`AstraZeneca Exhibit 2067 p. l
`InnoPharrna Licensing LLC v. AstraZeneca AB lPR2017-00905
`
`

`

`4/13/04 CANCERWK 19
`
`Page 2
`
`treated successfully, a large number of women still go on to be diagnosed with advanced breast cancer. The goal of
`
`treatment for these women is to achieve an effective disease response and to enable the patient to maintain good
`
`quality of life for as long as is feasibly possible.
`
`Hormonal agents such as aromatase inhibitors and tamoxifen are standard therapy in postmenopausal women with
`
`advanced breast cancer, providing an effective and well-tolerated treatment option. However, in time tumour cells can
`
`grow resistant to treatment with these hormonal therapies and as a result there is a need for new agents to which tumors
`
`are not resistant. Fulvestrant is an exciting new type of therapy, which brings new choices for women with advanced
`
`disease, extending the sequence of 'patient-friendly' hormonal therapies that can be used to control the disease.
`
`Fulvestrant works differently to any other treatment available, although like the other hormonal therapies it interferes
`
`with the effect of the homione 'estrogen' 011 tumour growth. Many breast cancers are dependent on the presence of
`
`estrogen to grow. Of the current therapies, aromatase inhibitors (e. g. Arimidex (anastrozole)) work by reducing the
`
`amount of estrogen in a woman's body, and tamoxifen (an anti-estrogen) blocks estrogen receptors. However, ta-
`
`moxifen also mimics some of the actions of estrogen, which can result in unwanted side effects. In contrast, fulvestrant
`
`works by blocking and removing the estrogen receptors in the breast cancer cells and, unlike tamoxifen, does not
`
`mimic the actions of estrogen.
`
`Fulvestrant offers durable responses and has tolerability benefits compared with aromatase inhibitors and tamoxifen.
`
`Fulvestrant is effective following disease progression on prior anti-estrogen and aromatase inhibitor therapy in addi-
`
`tion both therapies are effective following fulvestrant therapy. Fulvestrant therefore meets a key unmet need for
`
`women with advanced breast cancer, since it can be added in to the sequence of well-tolerated hormonal therapies and
`
`may delay the need to resort to cytotoxic chemotherapies with their well-recognized side effects.
`
`This article was prepared by Cancer Weekly editors from staff and other reports. Copyright 2004, Cancer Weekly via
`Newst.com & Newstnet.
`
`Copyright © 2004 Cancer Weekly via Newst.com & Newst.net
`
`---- INDEX REFERENCES ---
`
`COMPANY: ASTRAZENECA PLC
`
`NEWS SUBJECT: (Health & Family (1HE30); World Organizations (lIN77); European Union (lEU94))
`
`INDUSTRY: (Pharmaceuticals & Biotechnology (1PH13); Healthcare (lHE06); Endocrinology & Metabolism
`
`(lEN72); Internal Medicine (lIN54); Healthcare Practice Specialties (1HE49); Cancer Dmgs (lCA2l); Oncology &
`
`Hematology (lON95))
`
`REGION: (Western Europe (lWE4 1); Austria (1AU3 9); Scandinavia (lSC27); Germany (lGEl6); Europe (1EU83);
`
`Northern Europe (lNOO 1); Central Europe (lCE50))
`
`© 2015 Thomson Reuters. No Claim to Orig. US Gov. Works.
`
`AstraZeneca Exhibit 2067 p. 2
`
`

`

`4/13/04 CANCERWK 19
`
`Page 3
`
`Language: EN
`
`OTHER INDEXING: (ASTRAZENECA; EUROPEAN UNION; HUMBOLDT UNIVERSITY) (An'midex; Breast
`
`Cancer; Cancer Weekly; Commenting; Faslodex; Kurt Possinger)
`
`KEYWORDS: AstraZeneca; Therapy; Women's Health; All News; Consumer News; Oncology
`
`Word Count: 841
`
`4/13/04 CANCERWK l9
`
`END OF DOCUMENT
`
`© 2015 Thomson Reuters. No Claim to On'g. US Gov. Works.
`
`AstraZeneca Exhibit 2067 p. 3
`
`

This document is available on Docket Alarm but you must sign up to view it.


Or .

Accessing this document will incur an additional charge of $.

After purchase, you can access this document again without charge.

Accept $ Charge
throbber

Still Working On It

This document is taking longer than usual to download. This can happen if we need to contact the court directly to obtain the document and their servers are running slowly.

Give it another minute or two to complete, and then try the refresh button.

throbber

A few More Minutes ... Still Working

It can take up to 5 minutes for us to download a document if the court servers are running slowly.

Thank you for your continued patience.

This document could not be displayed.

We could not find this document within its docket. Please go back to the docket page and check the link. If that does not work, go back to the docket and refresh it to pull the newest information.

Your account does not support viewing this document.

You need a Paid Account to view this document. Click here to change your account type.

Your account does not support viewing this document.

Set your membership status to view this document.

With a Docket Alarm membership, you'll get a whole lot more, including:

  • Up-to-date information for this case.
  • Email alerts whenever there is an update.
  • Full text search for other cases.
  • Get email alerts whenever a new case matches your search.

Become a Member

One Moment Please

The filing “” is large (MB) and is being downloaded.

Please refresh this page in a few minutes to see if the filing has been downloaded. The filing will also be emailed to you when the download completes.

Your document is on its way!

If you do not receive the document in five minutes, contact support at support@docketalarm.com.

Sealed Document

We are unable to display this document, it may be under a court ordered seal.

If you have proper credentials to access the file, you may proceed directly to the court's system using your government issued username and password.


Access Government Site

We are redirecting you
to a mobile optimized page.





Document Unreadable or Corrupt

Refresh this Document
Go to the Docket

We are unable to display this document.

Refresh this Document
Go to the Docket