Published on March 18, 2010
Exhibit 99.1
FOR IMMEDIATE
RELEASE
NOVELOS
THERAPEUTICS DISCONTINUES CURRENT
DEVELOPMENT
PROGRAM FOR NOV-002 IN NSCLC
-
- - -
NOV-002
Phase 2 Development Continues in Breast Cancer Indication;
Seeking
to Build Clinical Stage Oncology Pipeline
NEWTON, Mass., March 18, 2010 –
Novelos Therapeutics, Inc. (OTCBB: NVLT), a biopharmaceutical company
focused on the development of therapeutics to treat cancer and hepatitis, today
announced that primary and secondary endpoints were not met in Novelos’ pivotal
Phase 3 trial in advanced non-small cell lung cancer (NSCLC) with its lead
product, NOV-002, in combination with first-line chemotherapy. Adding
NOV-002 to paclitaxel and carboplatin chemotherapy was not statistically or
meaningfully different in terms of efficacy-related endpoints or recovery from
chemotherapy toxicity versus chemotherapy alone. NOV-002 was safe, as
it did not add to the overall toxicity of chemotherapy. Detailed
trial results are expected to be presented at the 2010 annual meeting of the
American Society of Clinical Oncology (ASCO) taking place June 4-8 in Chicago,
Illinois.
This
randomized, controlled, open-label Phase 3 trial, conducted under a Special
Protocol Assessment (SPA) and Fast Track designation, enrolled 903 patients with
Stage IIIb/IV NSCLC and included all histological subtypes. The trial
encompassed approximately 100 clinical sites in 12 countries and evaluated
NOV-002 in combination with first-line paclitaxel and carboplatin chemotherapy
versus paclitaxel and carboplatin alone. The primary efficacy
endpoint of the trial was improvement in overall survival. Secondary
endpoints included progression free survival, response rate and duration of
response, recovery from chemotherapy-induced myelosuppression, determination of
immunomodulation, quality of life and safety. Based on results from
this Phase 3 trial, Novelos will discontinue development of NOV-002 for NSCLC in
combination with first-line paclitaxel and carboplatin
chemotherapy.
“We designed and
executed a robust Phase 3 NSCLC trial, but disappointingly, NOV-002 did not work
in this very difficult to treat indication in combination with this
chemotherapy,” said Harry Palmin, President and CEO of
Novelos. “Moving forward, our Phase 2 programs continue in cancer and
hepatitis with our oxidized glutathione-based compounds. We expect
results from an ongoing NOV-002 Phase 2 breast cancer trial in 3Q 2010, and are
scheduled to present new NOV-002 nonclinical data at the American Association
for Cancer Research (AACR) Annual Meeting in April 2010. We also
expect to initiate a Phase 2 hepatitis C trial shortly with our second compound
NOV-205. Meanwhile, we intend to rebuild our pipeline through
licensing or acquiring clinical-stage oncology compounds, utilizing our
experienced and proven development team.”
About
Novelos Therapeutics, Inc.
Novelos
Therapeutics, Inc. is a biopharmaceutical company commercializing oxidized
glutathione-based compounds for the treatment of cancer and
hepatitis. Novelos is seeking to build a pipeline through licensing
or acquiring clinical stage compounds or technologies for oncology
indications. Our lead compound, NOV-002, has been administered to
approximately 1,000 cancer patients in clinical trials and is in Phase 2
development for solid tumors in combination with
chemotherapy. Novelos has a partnership with Mundipharma, an
independent associated company of Purdue Pharma, to develop and commercialize
NOV-002 in Europe and Asia (excluding China). Novelos’ second
compound, NOV-205, which has been administered to approximately 200 hepatitis
patients in clinical trials, is in Phase 2 development for chronic hepatitis C
non-responders. Both compounds have been partnered with Lee’s Pharm
in China. For additional information about Novelos please visit www.novelos.com
|
COMPANY
Harry
S. Palmin, President and CEO
Ph:
617-244-1616 x11
Email:
hpalmin@novelos.com
|
INVESTOR
RELATIONS
Stephen
Lichaw
Ph:
201-240-3200
Email:
slichaw@novelos.com
|
Novelos
Therapeutics, Inc.
One
Gateway Center, Suite 504
Newton,
MA 02458
This
news release contains forward-looking statements. Such statements are
valid only as of today, and we disclaim any obligation to update this
information. These statements are subject to known and unknown risks
and uncertainties that may cause actual future experience and results to differ
materially from the statements made. These statements are based on
our current beliefs and expectations as to such future outcomes. Drug
discovery and development involve a high degree of risk. Factors that
might cause such a material difference include, among others, uncertainties
related to the ability to attract and retain partners for our technologies, the
identification of lead compounds, the successful preclinical development
thereof, the completion of clinical trials, the FDA review process and other
government regulation, our pharmaceutical collaborators’ ability to
successfully develop and commercialize drug candidates, competition from other
pharmaceutical companies, product pricing and third-party
reimbursement.
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