The proceeds will support BioCancell’s efforts to accelerate its clinical pipeline, with emphasis on a Phase IIb pancreatic cancer clinical trial. BC-819, BioCancell’s lead drug, recently completed a Phase I/IIa pancreatic cancer clinical trial, showing an excellent safety profile and significant preliminary efficiency. BioCancell is preparing an FDA application to commence an advanced, international Phase IIb clinical trial of BC-819 given in sequence with the FDA-approved cancer drug Gemzar, a combination that has shown better efficiency on animals than either of these drugs alone. BC-819 is also undergoing clinical trials for bladder cancer (Phase IIb) and ovarian cancer (Phase I/IIa).
BioCancell CEO Uri Danon stated, “We are pleased with the successful fundraising round, and thank the investors for their confidence in BioCancell. I am certain that this fundraising, as well as our recent, successful Phase I/IIa pancreatic cancer clinical trial, will help in advancing our clinical trials and proving the potential of BC-819. This fundraising accomplishment compels BioCancell to ensure even greater successes in the future.”
About BioCancell
BioCancell was founded in 2004, based on technology developed by Prof. Abraham Hochberg, a 20-year professor of molecular biology at the Hebrew University of Jerusalem. Prof. Hochberg is a founder of BioCancell and its Chief Scientist since inception. BioCancell specializes in developing treatments for a wide range of types of cancer.
BioCancell has developed a series of drugs that use plasmids (biological material) as a targeted treatment for cancer. Lead drug candidate BC-819 is based on the use of the H19 gene, expressed only in cancerous cells, to synthesize a toxin in the cancerous cells only, causing cancer cell destruction without significant side effects or damage to surrounding tissue.
Certain statements in this press release are forward-looking. These forward-looking statements are based on certain assumptions and reflect current expectations. As a result, forward-looking statements are subject to a number of risks and uncertainties that could cause actual results or events to differ materially from current expectations. Some of the factors that could cause actual results to differ materially from current expectations are discussed in materials that BioCancell from time to time files with, or furnishes to, the U.S. Securities and Exchange Commission. There is no assurance that any forward-looking statements will materialize. You are cautioned not to place undue reliance on forward-looking statements, which reflect expectations only as of the date of this press release. Except as may be required by applicable law, BioCancell disclaims any intention or obligation to update or revise any forward-looking statements.
Contact:
BioCancell Therapeutics Uri Danon, CEO Cell: +972-522-385-981 uri.danon@biocancell.com