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Pam Lord
Canale Communications
619-849-6003
plord@canalecomm.com
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Nereus Pharmaceuticals Completes Enrollment of Phase 2 ADVANCE Clinical Trial of Plinabulin in Non-Small Cell Lung Cancer
SAN DIEGO, Calif., June 22, 2010 – Nereus Pharmaceuticals, Inc.,
a pioneer in drug discovery and development from marine microbial sources,
announced completion of enrollment in the randomized Phase 2 ADVANCE study
evaluating its tumor selective vascular disrupting agent (VDA), plinabulin (NPI-2358),
in patients with non-small cell lung cancer (NSCLC) who have failed treatment with
chemotherapy. Approximately 170 patients were enrolled in this international
clinical trial. The study is comparing treatment with the standard of care drug
docetaxel alone versus docetaxel plus plinabulin. Interim data from the ADVANCE
study were presented at the 2010 American Society of Clinical Oncology Annual Meeting
in Chicago in early June.
In connection with the progress of its clinical programs, Nereus’ existing investors
have provided additional funding and commitments of up to an aggregate of $20 million.
This additional financing was led by HBM BioVentures and included Alta Partners,
Forward Ventures, Gimv, Advent International, Pacific Venture Group, Roche Venture Fund,
and Astellas Venture Management.
“Our dedicated investors are committed to see our programs through to important milestones,”
said President and CEO, Kobi M. Sethna.
In the ADVANCE trial, preliminary data on the primary efficacy endpoint of survival are
encouraging and continue to mature. Safety data are also notable in terms of suggesting
plinabulin’s excellent safety profile, inclusive of areas of concern with many oncology drugs
such as cardiac, neurologic and hematologic safety. Of significant interest, addition of plinabulin
appears to markedly improve the serious adverse effect of docetaxel on patients’ infection fighting
white blood cells. This is particularly important as chemotherapy induced neutropenia in cancer
patients is a significant source of morbidity and health care expenditures. Development of a drug
that treats tumors while improving this common problem could be a major advance in cancer chemotherapy.
Nereus’ second drug candidate, marizomib (NPI-0052), is a
second-generation inhibitor of the 20S proteasome. Marizomib also continues to progress in a number
of clinical trials in patients with multiple myeloma, lymphomas, and leukemias. Data from these
studies were presented at the 2009 American Society of Hematology Annual Meeting and 2009 EORTC-NCI-AACR
Symposium on Molecular Targets and Cancer Therapeutics.
“Nereus has made significant clinical progress with its anti-cancer agents, plinabulin and marizomib,
two highly differentiated product candidates that are progressing nicely through mid-stage clinical trials
towards pivotal studies,” said Matthew A. Spear, M.D., Chief Medical Officer of Nereus Pharmaceuticals, Inc.
“There is significant momentum behind our programs, fueled by enthusiasm from some of the top cancer experts
from around the world.”
About Plinabulin (NPI-2358)
Plinabulin is a potent, selective tumor vascular disrupting agent (VDA) and
one of over 200 synthetic analogues in the series that were prepared following the discovery of the parent
compound isolated from a marine fungus. Plinabulin has a dual effect on tumors: it selectively attacks
existing tumor blood vessels leading to tumor necrosis without affecting normal vasculature, and it has a
direct apoptotic effect on tumor cells. Preclinical data demonstrate favorable pharmacokinetic and pharmacodynamic
profiles and improvements in efficacy and tolerability when added to standard cancer therapies. Results from Phase 1
and Phase 2 clinical trials are clearly validating the translation of these findings into patients.
About Marizomib (NPI-0052)
Nereus’ novel, small molecule marizomib was
discovered from a new marine-obligate actinomycete (Salinispora tropica). Preclinical studies indicate this
potent proteasome inhibitor may be superior to other proteasome inhibitors with broader target inhibition, faster
onset and longer duration of action, higher potency, and oral availability that translate into decreasing toxicities
and overcoming resistance. Marizomib has shown preclinical activity against many common cancers, such as leukemias,
lymphomas and myeloma, including cells from patients who are resistant to newer cancer therapies and steroid therapy.
About Nereus Pharmaceuticals, Inc.
Nereus Pharmaceuticals pursues novel sources of chemical diversity to discover and
develop new therapeutics. Using its unmatched expertise in marine microbiology to identify unique biologically active
compounds, Nereus has two oncology drug candidates in clinical trials. Plinabulin (NPI-2358), a novel selective vascular
disrupting agent, is being evaluated in patients with solid tumors. The second-generation proteasome inhibitor marizomib (NPI-0052)
is being evaluated in patients with lymphomas, leukemias and multiple myeloma. The company’s discovery portfolio includes
potential drug candidates for cancer, infectious diseases and inflammation. For more information, visit www.nereuspharm.com.
Nereus Pharmaceuticals is a registered trademark of Nereus Pharmaceuticals, Inc.
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Nereus Pharmaceuticals is a registered trademark of Nereus Pharmaceuticals, Inc.
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