Novelos Therapeutics and Academic Collaborators Present Four Posters at AACR 2009 Annual Meeting
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New Mechanistic Findings with NOV-002 in Animal and Cellular Models NEWTON, Mass.--(Business Wire)-- Novelos Therapeutics, Inc. (OTCBB: NVLT), a biopharmaceutical company focused on the development of therapeutics to treat cancer and hepatitis, today announced that Novelos is presenting four scientific posters, based on collaborations with Drs. Qihong Huang and Kiranmai Gumireddy of the Wistar Institute, Philadelphia PA, and Drs. Kenneth Tew, Danyelle Townsend and Yefim Manevich of the Medical University of South Carolina, Charleston, SC, at the ongoing American Association for Cancer Research (AACR) 2009 Annual Meeting in Denver, CO. These four posters present findings in animal and cellular model systems that add to the understanding of the pharmacological actions of NOV-002 and how these may relate to its clinical profile in oncology patients. An abstract of each poster presentation has been published in the conference proceedings. NOV-002 is in a pivotal Phase 3 trial for non-small cell lung cancer under a Special Protocol Assessment (SPA) and Fast Track, which is expected to conclude in late 2009. NOV-002 has also demonstrated positive results in Phase 2 trials for other cancer indications. Inhibition of tumor cell invasion and ErbB2/PI3K signaling pathways by the glutathione disulfide-mimetic NOV-002 (Abstract #1807) Dr. Qihong Huang is presenting data showing that NOV-002 inhibited the ability of multiple human cancer cell types to invade extracellular matrix, apparently as a consequence of modulating the redox-sensitive signaling pathway that is known to control tumor metastasis in vivo. In vivo pharmacokinetic and pharmacodynamic behavior of NOV-002, a redox-modulating glutathione disulfide mimetic (Abstract #1728) Dr. Townsend`s presentation of results in mice describes plasma levels of oxidized and reduced glutathione and increased S-glutathionylation of specific plasma proteins (potential pharmacodynamic biomarkers) following parenteral administration of NOV-002 which indicate the generation of a mild and transient oxidative signal that may trigger a variety of redox-regulated biochemical cascades. Polymorphisms of GST pi: Redox regulation through protein S-glutathionylation (Abstract #2953) Dr. Townsend`s second poster includes data showing that S-glutathionylation of some proteins after treatment of transformed human cells with NOV-002 (in this poster GSSG) may require the activity of glutathione S-transferase pi, which is known to be elevated in many types of human tumors. NOV-002, a redox-modulating glutathione disulfide mimetic, leads to redox-mediated calcium influx and nitric oxide generation through eNOS activation in myeloid cells (Abstract #3762) Dr. Manevich is presenting data illustrating that modulation of cell surface redox status and transmembrane potential by NOV-002 in myeloid cells induces changes in calcium influx and subsequent NO generation which may be relevant to enhanced recovery from chemotherapy-induced myelosuppression seen in clinical studies of this drug candidate. "The data being presented at the AACR Annual Meeting suggest that NOV-002 may interfere with tumor metastasis, describe how redox signaling by NOV-002 in the plasma compartment may be transduced to other tissues, provide a possible predictive marker (GSTp) for responsiveness to NOV-002 and offer further evidence of cell signaling modulation by NOV-002 in both tumor and myeloid cells," said Christopher Pazoles, Ph.D., Vice President of Research & Development of Novelos. "This array of mechanism-related findings further expands our understanding of how redox modulation by NOV-002 may relate to its clinical profile in cancer patients." The posters are available at www.novelos.com `Our Products`, `NOV-002` section. About Novelos Therapeutics, Inc. Novelos Therapeutics, Inc. is a biopharmaceutical company commercializing oxidized glutathione-based compounds for the treatment of cancer and hepatitis. NOV-002, the lead compound currently in Phase 3 development for lung cancer under SPA and Fast Track, acts together with chemotherapy as a chemoprotectant and a chemopotentiator. NOV-002 is also in Phase 2 development for early-stage breast cancer and chemotherapy-resistant ovarian cancer. Novelos has a partnership with Mundipharma to develop and commercialize NOV-002 in Europe and Japan. Novelos` second compound, NOV-205, acts as a hepatoprotective agent with immunomodulating and anti-inflammatory properties. NOV-205 is in Phase 1b 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 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, ourpharmaceutical collaborators` ability to successfully develop and commercialize drug candidates, competition from other pharmaceutical companies, product pricing and third-party reimbursement. Novelos Therapeutics, Inc. COMPANY Harry S. Palmin, 617-244-1616 x11 President and CEO hpalmin@novelos.com or INVESTOR RELATIONS Stephen Lichaw, 201-240-3200 slichaw@novelos.com Copyright Business Wire 2009
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