NeoRx Expands Picoplatin Lung Cancer Clinical Trial Into Selected Eastern European Countries
25 Abril 2006 - 8:00AM
PR Newswire (US)
First Patient Treated with Picoplatin in Expanded Phase 2 Clinical
Trial of Small Cell Lung Cancer SEATTLE, April 25
/PRNewswire-FirstCall/ -- NeoRx Corporation (NASDAQ:NERX) today
announced the expansion of its Phase 2 clinical trial of picoplatin
for lung cancer into selected Eastern European countries with the
treatment of the first patients there. The open-label, multi-center
study of picoplatin, the Company's lead oncology therapeutic
candidate, is continuing to enroll patients with small cell lung
cancer (SCLC) at clinical sites in the United States and Canada.
Picoplatin is a new generation platinum therapy that provides a
differentiated spectrum of activity, reduced reactivity and an
improved safety profile. An intravenous chemotherapeutic agent,
picoplatin is designed to overcome platinum resistance associated
with the treatment of solid tumors. In addition, testing in more
than 500 patients in Phase 1 and 2 safety and efficacy studies
indicated that picoplatin has a more manageable safety profile with
fewer side effects than currently available platinum-based
therapies. "New drugs are urgently needed that are active in small
cell lung cancer and that can overcome the drug resistance that
occurs with currently available platinum compounds. We believe that
picoplatin is a promising agent for the treatment of this
aggressive and deadly form of lung cancer," said Jerry McMahon,
Ph.D., chairman and chief executive officer of NeoRx. "The
expansion of our Phase 2 trial into Eastern Europe is important
because small cell lung cancer is a serious disease in both North
America and Europe, allowing us to maximize access to patients on
both continents for our clinical study." Phase 2 Study Details The
ongoing Phase 2 clinical trial is designed to confirm and expand
data supporting the efficacy of picoplatin as a single agent in the
treatment of patients with platinum refractory or resistant SCLC.
Several efficacy endpoints are being assessed, including response
rates, progression-free survival, overall survival, improvement in
disease-related symptoms and disease control (defined as complete
response, partial response and stable disease). The trial is
currently being conducted at approximately 30 clinical sites in
Eastern Europe and approximately 30 sites in North America. About
Small Cell Lung Cancer SCLC is the most aggressive and deadly form
of lung cancer and accounts for approximately 20 percent of all
lung cancer cases. The estimated incidence of lung cancer was
383,900 in Europe in 2004, according to the International Agency
for Research on Cancer, and 174,500 in the United States in 2006,
according to the National Cancer Institute. Platinum-containing
combination chemotherapy is currently considered standard therapy.
However, toxicity, failure to respond to treatment (refractory
SCLC) or early relapse (resistant SCLC) can affect treatment
outcomes. After the failure of combination chemotherapy, there is
currently no available therapy that offers significant benefit to
patients who have refractory or resistant disease. About NeoRx
NeoRx is a specialty pharmaceutical company dedicated to the
discovery, development and commercialization of oncology drugs that
impact the lives of individuals afflicted with cancer. The Company
currently is focusing its development efforts on picoplatin, a new
generation platinum therapy that provides a differentiated spectrum
of activity, reduced reactivity and an improved safety profile. An
intravenous chemotherapeutic, picoplatin is designed to overcome
multiple mechanisms of platinum-based chemoresistance. NeoRx also
is collaborating with the Scripps Florida Research Institute on the
discovery of novel, small-molecule, multi-targeted protein kinase
inhibitors for the treatment of cancer. For more information, visit
http://www.neorx.com/. This release contains forward-looking
statements, including statements regarding the Company's business
model, drug development programs and clinical trial plans. The
Company's actual results may differ materially from those indicated
in these forward looking statements based on a number of factors,
including the Company's ability to timely complete, if at all, its
proposed $65 million equity financing, anticipated operating
losses, uncertainties associated with research, development,
testing and related regulatory approvals, future capital needs and
uncertainty of additional financing, competition, uncertainties
associated with intellectual property, dependence on third-party
manufacturers, suppliers and collaborators, lack of sales and
marketing experience, loss of key personnel, uncertainties
associated with market acceptance, technology change and government
regulation, and the other risks and uncertainties described in the
Company's current and periodic reports filed with the Securities
and Exchange Commission, including NeoRx's Annual Report on Form
10-K for the year ended December 31, 2005. Readers are cautioned
not to place undue reliance on these forward-looking statements,
which speak only as of the date of this release. The Company
undertakes no obligation to update any forward-looking statement to
reflect new information, events or circumstances after the date of
this release or to reflect the occurrence of unanticipated events.
DATASOURCE: NeoRx Corporation CONTACT: Julie Rathbun, Corporate
Communications of NeoRx Corporation, +1-206-286-2517, or Web site:
http://www.neorx.com/
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