Eisai to Present New Research on Halaven (Eribulin) at 35th Annual San Antonio Breast Cancer Symposium
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Eisai to Present New Research on Halaven (Eribulin) at 35th Annual San Antonio Breast Cancer Symposium

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2 pages
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Eisai to Present New Research on Halaven (Eribulin) at 35th Annual San Antonio Breast Cancer Symposium PR Newswire HATFIELD, England, November 28, 2012 HATFIELD, England, November 28, 2012 /PRNewswire/ -- For European Medical Media Only Eisai will be presenting six abstracts highlighting new study results for Halaven (eribulin) at the 2012 CTRC-AACR San Antonio Breast Cancer Symposium. The meeting will be held December 4-8, 2012 at the Henry B. Gonzalez Convention Center in San Antonio, Texas. These studies highlight Eisai's current and ongoing clinical research efforts with eribulin, reinforcing the company's commitment to continued research to patients and their families affected by metastatic breast cancer. Additionally, Phase III study results of the head-to-head study of eribulin vs capecitabine will be highlighted as part of a SABCS- sponsored conference to be held on 7 December, 2012. "As part of our human health care mission we strive to better understand the needs of patients and their families to help address unmet medical needs and increase the benefits that healthcare provides," said Kenichi Nomoto, Ph.D., President, Oncology Product Creation Unit at Eisai. "Our continued work to further understand the clinical profile of eribulin underscores our commitment to this important mission.

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Eisai to Present New Research on Halaven (Eribulin) at 35th Annual San Antonio Breast Cancer Symposium
PR Newswire HATFIELD, England, November 28, 2012
HATFIELD, England,November 28, 2012/PRNewswire/ --
For European Medical Media Only
Eisai will be presenting six abstracts highlighting new study results for Halaven (eribulin) at the 2012 CTRC-AACR San Antonio Breast Cancer Symposium. The meeting will be heldDecember 4-8, 2012at the Henry B. Gonzalez Convention Center in San Antonio, Texas.
These studies highlight Eisai's current and ongoing clinical research efforts with eribulin, reinforcing the company's commitment to continued research to patients and their families affected by metastatic breast cancer. Additionally, Phase III study results of the head-to-head study of eribulin vs capecitabine will be highlighted as part of a SABCS-sponsored conference to be held on7 December, 2012.
"As part of ourhuman health caremission we strive to better understand the needs of patients and their families to help address unmet medical needs and increase the benefits that healthcare provides," said Kenichi Nom oto, Ph.D., President, Oncology Product Creation Unit at Eisai. "Our continued work to further understand the clinical profile of eribulin underscores our commitment to this important mission."
The following Eisai abstracts have been accepted for presentation at this year's San Antonio Breast Cancer Symposium:
 Product Abstract Name  A Phase III, open-label, randomized, multicenter study of  Eribulin eribulin mesylate versus capecitabine in patients with  Session: locally advanced or metastatic breast cancer previously  S6-6 treated with anthracyclines and taxanes  Oral Presentation  Eribulin Results of a Phase II, multicenter, single-arm study of  Abstract No: eribulin mesylate as first-line therapy for locally  P1-12-02 recurrent or metastatic HER2-negative breast cancer  Poster Session  Eribulin Eribulin mesylate + trastuzumab as first-line therapy for  Abstract No: locally recurrent or metastatic HER2-positive breast  P5-20-04 cancer: results from a Phase II, multicenter, single-arm  study  Poster Session  Eribulin Adjuvant treatment of early-stage breast cancer with  Abstract No: eribulin mesylate following dose-dense doxorubicin and  P1-13-11 cyclophosphamide: preliminary results from a Phase II,  single-arm feasibility study  Poster Session  Eribulin Post-hoc safety and tolerability assessment in patients  Abstract No. receiving palliative radiation during treatment with  P6-11-14 eribulin mesylate for metastatic breast cancer  Poster Session  N/A Family Members' Burden in Patients with Metastatic and  Abstract No: Early Stage Breast Cancer  P6-09-06 Poster Session
The information discussed in this release is about investigational uses for eribulin. InEurope, eribulin is indicated for the treatment of patients with locally advanced or metastatic breast cancer who have progressed after at least two chemotherapeutic regimens for advanced disease. Prior therapy should have included an anthracycline and a [1] taxane unless patients were not suitable for these treatments. It is not intended to convey conclusions of efficacy and safety.
Notes to Editors
® Halaven(eribulin)
- ENDS -
Eribulin is a non-taxane, microtubule dynamics inhibitor indicated for the treatment of patients with breast cancer who have previously received at least two chemotherapeutic regimens for metastatic disease and whose prior
therapy should have included an anthracycline and a taxane. Eribulin belongs to a class of antineoplastic agents, the halichondrins, which are natural products, isolated from the marine sponge Halichondria okadai. It is believed to work by inhibiting the growth phase of microtubule dynamics without affecting the shortening phase and sequesters tubulin into non-productive aggregates.
Halaven is approved in the European Union, USA, Switzerland, Japan, and Singapore. Halaven has received pricing authorisation and been launched in Austria, Canada, Denmark, Finland, Germany, Iceland, Italy, Norway, Russia, South Korea, Sweden, Switzerland, Slovenia, and the UK.
Metastatic Breast Cancer
Metastatic breast cancer is an advanced stage of the disease that occurs when cancer spreads beyond the breast to other parts of the body. In Europe, approximately 6% of breast cancers are metastatic at diagnosis with a five-[2] year survival rate of 21%.
Eisai in Oncology
Our commitment to meaningful progress in oncology research, built on scientific expertise, is supported by a global capability to conduct discovery and preclinical research, and develop small molecules, therapeutic vaccines, and biologic and supportive care agents for cancer across multiple indications.
About Eisai
Eisai recently expanded their UK Hatfield commercial, research and manufacturing facility which now supports the company's growing EMEA business.
Eisai concentrates its R&D activities in three key areas:
Neuroscience, including: Alzheimer's disease, epilepsy, pain and weight loss Oncology including: anticancer therapies; tumour regression, tumour suppression, antibodies, etc. Vascular/Immunological reaction including: thrombocytopenia, rheumatoid arthritis, psoriasis, inflammatory bowel disease
With operations in the U.S., Asia, Europe and its domestic home market of Japan, Eisai employs more than 11,000 people worldwide. In Europe, Eisai undertakes sales and marketing operations in over 20 markets, including the United Kingdom, France, Germany, Italy, Spain, Switzerland, Sweden, Ireland, Austria, Denmark, Finland, Norway, Portugal, Iceland, Czech Republic, Slovakia, the Netherlands, Belgium, Luxembourg, the Middle East and Russia.
For further information please visit our web sitehttp://www.eisai.com.
References
1. Halaven (eribulin) Summary of Product Characteristics available from: http://www.medicines.org.uk/emc/medicine/24382(Last accessedNovember 2012)
2. Cardoso, M. and Castiglione F. Locally recurrent or metastatic breast cancer: ESMO Clinical Recommendations for diagnosis, treatment and follow -up. On behalf of the ESMO Guidelines Working Group. Ann Oncol (2009) 20 (suppl 4): iv15-iv18
Date of preparation:November 2012
Job code: Halaven-UK0069
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