Entest BioMedical Updates Status of Proposed Medistem Transaction, Discusses Potential Revenue Streams
SAN DIEGO, CA--(Marketwire - May 12, 2010) - Entest BioMedical, Inc. (
Medistem has a portfolio of products in various stages of development covered by 15 families of patent applications and has filed an Investigational New Drug (IND) Application with the FDA for use of its Endometrial Regenerative Cells for the treatment of critical limb ischemia, a form of peripheral artery disease. Medistem's Endometrial Regenerative Cell (ERC) is a "universal donor" stem cell that is capable of differentiating into heart, bone, muscle, blood vessel, lung, brain, liver, and islet cells.
David Koos, Chairman & CEO of Entest BioMedical, stated, "We are currently reviewing Medistem's operations as part of our due diligence. Both Dr. Thomas Ichim, CEO of Medistem, and myself have been studying how Medistem's intellectual properties may dovetail into Entest's treatment models and are both extremely excited about the prospects of a combined entity . We believe that Medistem's ERC stem cells could become an important component of Entest's therapeutic treatment for Chronic Obstructive Pulmonary Disease (COPD). The ERC appears to facilitate the regeneration of blood vessels, a critical factor in curing COPD. We look forward to working jointly towards cures for COPD, Critical Limb Ischemia and an Immunotherapeutic cancer vaccine for animals."
A spokesperson for Entest noted that the contemplated acquisition has the potential to generate a term revenue stream as a result of reagent sales of Medistem's ERC stem cell. Entest anticipates being able to market 2,000 units of the ERC stem cell reagents within 12 months of this transaction at $500 per unit.
The proposed acquisition contemplated by the LOI is subject to the parties entering into a definitive agreement and the satisfaction of the terms and conditions of that agreement.
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