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Roche Holding AG

New Hope in Fight Against Advanced Lung Cancer

Basel, Switzerland (ots/PRNewswire)

- Roche files marketing application for Tarceva with European
health authorities
Roche today submitted a Marketing Authorisation Application to the
European health authorities for its new cancer drug Tarceva
(erlotinib) for the treatment of advanced non-small cell lung cancer
(NSCLC). NSCLC is the most common form of lung cancer, which in
itself is the most frequent cancer world wide. The application is
based on data from a pivotal clinical trial involving more than 700
patients with advanced NSCLC who had failed first or second-line
chemotherapy. Patients with advanced NSCLC treated with Tarceva
achieved a significant improvement (42%) in survival compared to
those on placebo, along with improved symptom benefit(1).
"The benefits of Tarceva in this patient group are very
compelling. Tarceva represents the first significant advance in
survival, among targeted therapies, for lung cancer patients who have
failed available chemotherapy. In the study, one out of three
patients on Tarceva were alive at one year as opposed to only one of
five in the placebo group. We will work closely with regulatory
authorities to bring Tarceva to patients as quickly as possible" said
William M Burns, Head of Roche Pharmaceuticals Division.
Lung cancer is the most common cancer worldwide, accounting for
1.2 million new cases annually(2) with someone, somewhere dying of
lung cancer every 30 seconds (3). NSCLC accounts for almost 80
percent of all types of lung cancer and has few treatment options.
Tarceva is the first and only EGFR-targeted anticancer treatment
to have shown a significant survival prolongation in lung cancer. An
application for approval of Tarceva in advanced NSCLC was also filed
with the US FDA this month.
Study Details
The EU filing is based on results of the pivotal Phase III
randomised trial (BR21) involving 731 patients, which compared the
use of Tarceva versus placebo for the treatment of patients with
advanced NSCLC, following failure of first or second-line
chemotherapy. Patients receiving Tarceva lived significantly longer
than those in the placebo arm (6.7 months vs 4.7 months), an
improvement of 42%.1 The study also met all of its secondary
endpoints including improving time to symptomatic deterioration,
progression-free survival and response rate. In addition, there was a
45% improvement in survival at one year and further analysis showed
treatment benefit over a broad spectrum of patients.
About Tarceva
Tarceva is an investigational small molecule that targets the
human epidermal growth factor receptor (HER1) pathway. HER1, also
known as EGFR, is a key component of this signalling pathway, which
plays a role in the formation and growth of numerous cancers. Tarceva
blocks tumour cell growth by inhibiting the tyrosine kinase activity
of the HER1 signalling pathway inside the cell. Results of a Phase
III trial of Tarceva in pancreatic cancer are expected during the
second half of 2004 and Tarceva is currently being evaluated in an
extensive clinical development program by a global alliance among OSI
Pharmaceuticals, Genentech, and Roche. Chugai is pursuing its
development and regulatory approval for the Japanese market.
Roche in Oncology
Within the last five years the Roche Group including its partners
Genentech in the US and Chugai in Japan has become the world's
leading provider of anti-cancer treatments, supportive care products
and diagnostics. Its oncology business includes an unprecedented four
marketed products with survival benefit in different major tumour
indications: Xeloda and Herceptin in advanced stage breast cancer,
MabThera in non-Hodgkin's lymphoma, and Avastin in colorectal
carcinoma. In the United States Herceptin, MabThera and Avastin are
marketed either by Genentech alone or together with Biogen Idec Inc.
Outside of the United States, Roche and its Japanese partner Chugai
are responsible for the marketing of these drugs.
The Roche oncology portfolio also includes NeoRecormon (anaemia in
various cancer settings), Bondronat (prevention of skeletal events in
breast cancer and bone metastases patients, hypercalcaemia of
malignancy), Kytril (chemotherapy and radiotherapy-induced nausea and
vomiting) and Roferon-A (hairy cell and chronic myeloid leukaemia,
Kaposi's sarcoma, malignant melanoma, renal cell carcinoma). CERA is
the most recent demonstration of the commitment to anaemia
management. The Roche Group's cancer medicines generated sales of
more than 3.3 billion Swiss francs in the first half of 2004.
Roche is developing new tests, which will have a significant
impact on disease management for cancer patients in the future. With
a broad portfolio of tumour markers for prostate, colorectal, liver,
ovarian, breast, stomach, pancreas and lung cancer, as well as a
range of molecular oncology tests, we will continue to be the leaders
in providing cancer focused treatments and diagnostics.
Roche Oncology has four research sites (two in the US, Germany and
Japan) and four Headquarter Development sites (two in the US, UK and
Switzerland).
About Roche
Headquartered in Basel, Switzerland, Roche is one of the world's
leading innovation-driven healthcare groups. Its core businesses are
pharmaceuticals and diagnostics. Roche is number one in the global
diagnostics market, the leading supplier of pharmaceuticals for
cancer and a leader in virology and transplantation. As a supplier of
products and services for the prevention, diagnosis and treatment of
disease, the Group contributes on a broad range of fronts to
improving people's health and quality of life. Roche employs roughly
65,000 people in 150 countries. The Group has alliances and R&D
agreements with numerous partners, including majority ownership
interests in Genentech and Chugai.
All trademarks used or mentioned in this release are legally
protected.
Further information:
Reference:
1. Shepherd, F.; A randomized placebo-controlled trial of
erlotinib in patients with advanced non-small cell lung cancer
(NSCLC) following failure of 1st line or or 2nd line chemotherapy. A
National Cancer Institute of Canada Clinical Trials Group (NCIC).
(Abstract #7022), ASCO 2004.
2. World Health Organisation, World Cancer Report, 2003.
3. www.lungcancercoalition.org/cancer_facts.html.

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