PharmaGap Inc. Announces Successful Completion of Liposomal Development With Significantly Improved Potency of Cancer Drug
This development program has involved the production of a number of prototype designs, each at a range of drug concentrations within the liposome carrier. These prototypes were tested for potency across a 3 human bladder cancer and 3 human ovarian cancer cell lines, and compared head to head with the GAP-107B8 peptides alone (basic and enhanced versions), and with the empty liposome carriers. This testing was carried out at PharmaGap labs over the past 6 months. The liposome formulations and the enhanced version of GAP-107B8 represent novel and material new intellectual property for PharmaGap, and is the subject of a patent filing for the Company.
Dr. Ken Sokoll, Vice President of Clinical Development and Chief Operating Office for PharmaGap, stated "I am very pleased that we have achieved our objective of successfully identifying a liposomal formulation of both versions of our lead cancer drug, in the time frame established when we embarked on this program in the first quarter of the year. We now are presented with the prospect of a widened therapeutic window, and are seeing in vitro effectiveness at dose ranges suitable to proceed to human clinical trials. This has been a very labour intensive effort both internally by our staff as well as at our contractor sites, and I want to thank each of them for a high degree of effort and diligence in arriving at this key point in our program."
The successful development of the liposomal formulations of basic and enhanced GAP-107B8 has significantly widened the GAP-107B8 Therapeutic Window (the range of doses between the lowest effective dose and the highest dose where unacceptable toxicity become evident), which is a key consideration for effective clinical trial design and ultimate success of the drug in the marketplace.
Liposomal delivery systems are an accepted, proven, and commercially viable strategy for the formulation of pharmaceuticals for clinical use. These delivery systems are employed to improve tumour targeting, modulate the pharmacokinetics of the active agent and enhance its stability following administration. Therapeutic activity may be improved by modulating drug exposure and accumulation (controlled release) in the region where the target cells are located.
The two formulated GAP-107B8 compounds will now both proceed through in vivo pharmacokinetic and pharmacodynamic testing (to assess physical characteristic of the drug in a live system), as well as the determination of Maximum Tolerated Dose, in order to determine the optimum dose ranges for use in the in vivo efficacy testing of both formulations in bladder cancer (using intravesical administration) and ovarian cancer (using intraperitoneal administration) in the 4th quarter of this year.
About PharmaGap Inc.
PharmaGap Inc. (TSX-V: GAP.V - News), based in Ottawa, ON, is a biotechnology company with a core focus on developing novel peptide therapeutics for the treatment of cancer. PharmaGap's GAP-107B8 is a novel peptide drug that has been shown to be highly cytotoxic to numerous cancer types, including chemo-resistant cancers, in vitro. For more information on PharmaGap please visit the Company's website at www.pharmagap.com.
Forward Looking Statements
This news release contains certain statements that constitute forward-looking statements as they relate to the Company and its management. Forward-looking statements are not historical facts but represent management's current expectations of future events, and can be identified by words such as "believe", "expects", "will", "intends", "plans", "projects", "anticipates", "estimates", "continues", and similar expressions. Although management believes that expectations represented in such forward-looking statements are reasonable, there can be no assurance that they will prove to be correct.
By their nature, forward-looking statements include assumptions and are subject to inherent risks and uncertainties that could cause actual future results, conditions, actions or events to differ materially from those in the forward-looking statements. If and when forward-looking statements are set out in this news release, PharmaGap will also set out the material risk factors or assumptions used to develop the forward-looking statements. Except as expressly required by applicable securities laws, the Company assumes no obligation to update or revise any forward-looking statements. The future outcomes that relate to forward-looking statements may be influenced by many factors, including, but not limited to: results of ongoing product testing and development; regulatory approvals required to complete development of products; ability to manufacture product at quality and scale for human use on an economically sound basis; patient reimbursement by private and public health insurance programs; unintended side effects of products; competitive products; product liability; intellectual property; reliance on key personnel; risks of future legal proceedings; income tax matters; availability and terms of financing; distribution of securities; effect of market interest rates on price of securities, and potential dilution.
Note: Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release. No Securities Commission or other regulatory authority having jurisdiction over PharmaGap has approved or disapproved of the information contained herein. This release contains forward looking statements that may not occur or may change materially.
Contact:
PharmaGap Inc.Robert McInnisPresident & CEO613-990-9551bmcinnis@pharmagap.com