SOURCE: Cleveland BioLabs, Inc.

Cleveland BioLabs, Inc.

Cleveland BioLabs, Inc.

November 13, 2014 10:21 ET

Cleveland BioLabs and Roswell Park Cancer Institute Announce Publication of Studies Demonstrating Curaxin CBL0137's Ability to Eradicate Drug-Resistant Cancer Stem Cells and Potentiate Efficacy of Gemcitabine in Preclinical Models of Pancreatic Cancer

BUFFALO, NY--(Marketwired - Nov 13, 2014) - Cleveland BioLabs, Inc. (NASDAQ: CBLI) and Roswell Park Cancer Institute (RPCI) today announced the publication of studies in Oncotarget describing the preclinical efficacy of Curaxin CBL0137 as a single agent and in combination with the current standard-of-care therapy, gemcitabine, against different models of pancreatic ductal adenocarcinoma (PDA), including models of gemcitabine-resistant tumors. The reported studies were conducted by scientists at Roswell Park, SUNY Downstate Medical Center and Buffalo Biolabs, LLC.

Pancreatic cancer is the fourth leading cause of cancer-related death in the United States and is one of the few cancers for which survival has not improved substantially over nearly 40 years. Pancreatic cancer has the highest mortality rate of all major cancers; 94% of pancreatic cancer patients will die within five years of diagnosis (American Cancer Society: Cancer Facts & Figures 2014).

CBL0137 is a small molecule that modulates several important signaling pathways involved in the pathogenesis of PDA through inhibition of chromatin remodeling complex, also known as FACT. FACT has recently been shown to be a novel target in cancer due to its frequent overexpression in multiple tumor types.1 Tumor cells, but not normal cells, are dependent on FACT function for survival.1 FACT-positive tumors are associated with an aggressive malignant phenotype (high-grade, metastatic disease, worse overall survival).1 Research has shown that FACT is expressed in the majority of cases of PDA.1 One of the most significant factors predisposing patients to PDA is chronic pancreatic inflammation accompanied by constitutive activity of NF-kappaB.5 In addition, the heat shock response stress pathway, which is mediated by HSF1, is also frequently overactive in PDA cells.6  Inhibition of FACT inhibits cellular stress pathways mediated by NF-kappaB and HSF-1.2,3,4 FACT inhibition also activates the pro-apoptotic factor p53.2,3,4

In the published studies, the effect of CBL0137 monotherapy or in combination with gemcitabine was evaluated using patient-derived PDA xenografts and PANC-1 orthotopic tumors. In addition, potential mechanisms for the combined efficacy observed between CBL0137 and gemcitabine were investigated. CBL0137 was efficacious against mouse models of PDA and enhanced the effect of gemcitabine by causing a significant delay in tumor relapse following the completion of treatment. The data presented in the publication suggest that these combined effects may be a result of CBL0137 targeting of PDA cancer stem cells, as well as its modulation of the expression of genes that affect gemcitabine sensitivity in PDA cells. CBL0137 also demonstrated anti-tumor effects in models of gemcitabine-resistant tumors.

A Phase 1 trial assessing the intravenous administration of Curaxin CBL0137 in patients with metastatic or unresectable advanced solid cancers and lymphomas is underway in multiple centers in the United States, including RPCI. A Phase 1 study assessing the oral administration of Curaxin CBL0137 in patients with advanced solid tumors that are resistant or refractory to current standard treatment is being conducted in several centers in the Russian Federation. 

Wen Wee Ma, M.B.B.S., Associate Professor of Oncology in the Department of Medicine at RPCI and Principal Investigator for the intravenous trial of CBL0137, stated, "Pancreatic cancer is a very challenging disease that is highly resistant to conventional chemotherapy. CBL0137 has been shown to be effective in preclinical pancreatic cancer models, including gemcitabine-resistant tumors. The agent seems to target pancreatic cancer stem cells and survival pathways, thus rendering this a very promising treatment for this disease."

Andrei Gudkov, Ph.D., D.Sci., Senior Vice President of Basic Science at Roswell Park Cancer Institute and Chief Scientific Officer of Cleveland BioLabs, commented, "These data reinforce our growing base of evidence regarding the potentially broad efficacy of Curaxin CBL0137's mechanism of action. The data shared in this publication and the known role of FACT in the pathogenesis of PDA and viability of cancer stem cells support our consideration of pancreatic cancer as a potential indication for Phase 2 development of CBL0137." 

The Oncotarget publication may be found online at: http://impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path[]=2701

References:
1 Garcia et al. FACT is an "accelerator" of tumor transformation and potential marker and target of aggressive cancers. Cell Reports. 2013; 4: Published online June 3.
2 Gasparian et al. Curaxins: Anticancer Compounds That Simultaneously Suppress NF-kappaB and Activate p53 by Targeting FACT. Sci Transl Med. 2011; 3(95):95ra74
3 Neznanov et al. Anti-malaria drug blocks proteotoxic stress response: anticancer implications. Cell Cycle. 2009; 8(23):3960-3970
4 Neznanov et al. Proteotoxic stress targeted therapy: induction of protein misfolding enhances the antitumor effect of the proteasome inhibitor bortezomib. Oncotarget. 2011; 2(3):209-221 
5 Holcomb B, Yip-Schneider M and Schmidt CM. The role of nuclear factor kappaB in pancreatic cancer and the clinical applications of targeted therapy. Pancreas. 2008; 36(3):225-235
6 Xia Y, Rocchi P, Iovanna JL and Peng L. Targeting heat shock response pathways to treat pancreatic cancer. Drug discovery today. 2012; 17(1-2):35-43.

About Cleveland BioLabs, Inc.
Cleveland BioLabs, Inc. is an innovative biopharmaceutical company seeking to develop first-in-class pharmaceuticals designed to address diseases with significant medical need. The company's lead product candidates are entolimod, which is being developed as radiation countermeasure and a potential cancer treatment, and Curaxin CBL0137, our lead oncology product candidate. The company conducts business in the United States and in the Russian Federation through our three operating subsidiaries, Incuron, LLC, BioLabs 612, LLC and Panacela Labs, Inc. The company maintains strategic relationships with the Cleveland Clinic, Roswell Park Cancer Institute, and the Children's Cancer Institute Australia. To learn more about Cleveland BioLabs, Inc., please visit the Company's website at http://www.cbiolabs.com.

About Roswell Park Cancer Institute
The mission of Roswell Park Cancer Institute (RPCI) is to understand, prevent and cure cancer. Founded in 1898, RPCI is one of the first cancer centers in the country to be named a National Cancer Institute-designated comprehensive cancer center and remains the only facility with this designation in Upstate New York. The Institute is a member of the prestigious National Comprehensive Cancer Network, an alliance of the nation's leading cancer centers; maintains affiliate sites; and is a partner in national and international collaborative programs. For more information, visit www.roswellpark.org, call 1-877-ASK-RPCI (1-877-275-7724) or email askrpci@roswellpark.org. Follow Roswell Park on Facebook and Twitter.

This press release contains certain forward-looking information about Cleveland BioLabs that is intended to be covered by the safe harbor for "forward-looking statements" provided by the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. Words such as "expect(s)," "feel(s)," "believe(s)," "will," "may," "anticipate(s)" and similar expressions are intended to identify forward-looking statements. These statements include, but are not limited to, statements regarding our ability to successfully develop and commercialize our therapeutic products; our ability to expand our long-term business opportunities; the conduct and results of our various clinical trials; financial projections and estimates and their underlying assumptions; and future performance. All of such statements are subject to certain risks and uncertainties, many of which are difficult to predict and generally beyond the control of the Company, that could cause actual results to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. 

These factors include, among others, the Company's failure to successfully and timely develop new products; the Company's collaborative relationships and the financial risks related thereto; the Company's ability to comply with its obligations under license agreements; the risks inherent in the early stages of drug development and in conducting clinical trials; the Company's inability to obtain regulatory approval in a timely manner or at all; the Company's history of operating losses and the potential for future losses, which may lead the Company to not be able to continue as a going concern; the Company's need for substantial additional financing to meet its business objectives; the potential for the loss of funding from the Company's R&D grants and contracts and its ability to win additional funding under such grants and contracts. Some of these factors could cause future results to materially differ from the recent results or those projected in forward-looking statements. See also the "Risk Factors" and "Forward-Looking Statements" described in the Company's periodic filings with the Securities and Exchange Commission.

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