RYE, New York, Sept. 16, 2013 — Curemark LLC announced that CEO Dr. Joan Fallon will deliver the keynote at BioForward’s BioScience Vision Summit in Madison, WI on September 18. Life science entrepreneurs from across the country will attend the event, which focuses on biotechnology partnerships and innovation.
Dr. Fallon’s address, “Growth by Association: Winning through Public and Private Partnerships,” will highlight the clear benefits of the collaboration of government and business with life sciences stakeholders. Dr. Fallon’s Wisconsin speech comes on the heels of her speech to the White House Office of Technology and Science, attended by senior Obama Administration officials.
Dr. Fallon stated that, “I’m delighted and honored to be asked to deliver the keynote address at such an important conference and looking forward to meeting thought leaders from across the life sciences sector.”
“Wisconsin is a center of innovation for the biosciences, which is why this conference is extremely important. Patients want help, particularly for the large number of still-unmet medical needs. We need novel solutions and new thinking to move biotechnology forward,” Dr. Fallon continued.
Curemark is a drug research and development company focused on the treatment of neurological and other diseases, especially those with dysautonomic components, by addressing certain key gastrointestinal/pancreatic secretory deficiencies. The company previously announced that its Phase III double blind randomized placebo controlled multicenter clinical trial of CM-AT for autism met its primary and secondary endpoints. To learn more about our innovative science, visit www.curemark.com
This news release contains forward-looking statements that involve risks and uncertainties that could cause our actual results and experiences to differ materially from anticipated results and expectations expressed in such forward-looking statement. These forward-looking statements include, without limitation, statements regarding the mechanism of action of the Curemark products CM-AT, CM-4612 and CM-182 their potential advantages, their potential for use in treating diseases or disorders, as well as the timing, progress and anticipated results of the clinical development and regulatory processes concerning the Curemark products CM-AT, CM-4612 and CM-182. These statements are based on our current beliefs and expectations as to such future outcomes, and are subject to known and unknown risks and uncertainties that may cause actual future experience and results to differ materially from the statements made. Factors that might cause such a material difference include, among others, risks that the results of clinical trials will not support our claims or beliefs concerning the effectiveness of the Curemark products CM-AT, CM-4612 and CM-182, our ability to finance our development of CM-AT, CM-4612 and CM-182 regulatory risks, and our reliance on third party researchers and other collaborators. We assume no obligation to update these statements, except as required by law.