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	<title>CLEAR THERAPEUTICS, INC.</title>
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		<title>Scientific Advisory Board</title>
		<link>http://www.cleartherapeutics.com/scientific-advisory-board</link>
		<comments>http://www.cleartherapeutics.com/scientific-advisory-board#comments</comments>
		<pubDate>Tue, 30 Mar 2010 06:53:30 +0000</pubDate>
		<dc:creator>GalBitan</dc:creator>
				<category><![CDATA[Scientific Advisory Board]]></category>

		<guid isPermaLink="false">http://www.cleartherapeutics.com/?p=102</guid>
		<description><![CDATA[Karen Hsiao Ashe, MD, PhD received an A.B. in chemistry and physics from Harvard University, a Ph.D. in brain and cognitive sciences from the Massachusetts Institute of Technology, and an M.D. from Harvard Medical School. After completing a medical internship and neurology residency at the University of California, San Francisco, she conducted postdoctoral research on prions [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.cleartherapeutics.com/wp-content/gallery/sab/headshot.jpg"><img class="alignleft" style="margin-left: 5px; margin-right: 5px;" title="Karen Hsiao Ashe" src="http://www.cleartherapeutics.com/wp-content/gallery/sab/headshot.jpg" alt="Karen Hsiao Ashe" width="69" height="104" /></a><strong>Karen Hsiao Ashe, MD, PhD </strong>received an A.B. in chemistry and physics from Harvard University, a Ph.D. in brain and cognitive sciences from the Massachusetts Institute of Technology, and an M.D. from Harvard Medical School. After completing a medical internship and neurology residency at the University of California, San Francisco, she conducted postdoctoral research on prions under the guidance of Dr. Stanley Prusiner. She holds joint appointments in the Neurology Department at the University of Minnesota and the Minneapolis VA Medical Center’s Geriatric Research Education and Clinical Center. Occupying the Edmund Wallace and Anne Marie Tulloch Chairs in Neurology and Neuroscience, she directs the N. Bud Grossman Center for Memory Research and Care at the University of Minnesota. Using transgenic mouse models of Alzheimer’s disease, Dr. Ashe’s research focuses on the mechanisms by which the tau and Aß proteins disrupt brain function.  Dr. Ashe’s recent discoveries include the memory-impairing Aß*56 protein assembly and proof that neurofibrillary tangles are not a cause of memory loss in mice. She has received numerous honors for her contributions, including the MetLife Foundation Award for Medical Research in 2005, the Potamkin Prize from the American Academy of Neurology in 2006, and induction into the Institute of Medicine of the National Academies of the United States of America in 2009.</p>
<p><a href="http://www.cleartherapeutics.com/wp-content/gallery/sab/john-c-chabala.jpg"><img class="alignleft" style="margin-left: 5px; margin-right: 5px;" title="John Chabala" src="http://www.cleartherapeutics.com/wp-content/gallery/sab/john-c-chabala.jpg" alt="Jack Chabala" width="69" height="86" /></a><strong>John C. Chabala</strong>, <strong>PhD</strong> earned a B.S. degree in chemistry at Bucknell University in 1970 and a Ph.D. in organic chemistry at the Massachusetts Institute of Technology in 1975.  He joined Merck Sharp &amp; Dohme Research laboratories in 1974 and rose to the position of Executive Director of Basic Chemistry where he supervised the research of three departments of medicinal chemistry, as well as natural products chemistry and biophysical chemistry.  He is the co-inventor of ivermectin, a highly successful parasiticide, for which he was awarded the Thomas Alva Edison Patent Award in 1987 and the New Jersey Institute of Chemistry Award in 1992.  In 1991 he joined Bristol-Myers Squibb where he was Senior Vice President and worldwide head of medicinal chemistry.  In 1993 he was a co-founder of Pharmacopeia, Inc., a pioneer in combinatorial chemistry and its application to the discovery and optimization of novel drugs.  At Pharmacopeia he was President, Chief Scientific Officer, and a member of the Board of Directors, and oversaw the growth of the company from a privately held concern to a publicly traded company.  Since 1997 Dr. Chabala has served as member of the Scientific Advisory Board of 15 biotechnology companies and as an independent consultant for 17 biotechnology companies, the Cystic Fibrosis Foundation, the Hereditary Disease Foundation and three venture capital groups.</p>
<p><strong><a href="http://www.cleartherapeutics.com/wp-content/gallery/sab/chesselet-pic-matisse-t.jpg"><img style="float: left; margin-left: 5px; margin-right: 5px; border: 0px initial initial;" title="Marie-Françoise Chesselet" src="http://www.cleartherapeutics.com/wp-content/gallery/sab/chesselet-pic-matisse-t.jpg" alt="Marie-Françoise Chesselet" width="69" height="68" /></a>Marie-Françoise Chesselet, MD, PhD</strong> is the Charles H. Markham Professor of Neurology and the Chair of the Department of Neurobiology in the David Geffen School of Medicine at UCLA. She received her MD and PhD degrees from the University of Paris VI, France, where she completed her PhD thesis in the laboratory of Jacques Glowinski and became a Charge de Recherches at the CNRS, the National French Research Agency. She was a Visiting Scientist in the laboratories of Ann Graybiel at MIT and of Michael Bronstein at the NIH before joining the Faculty of the Medical College of Pennsylvania and then the University of Pennsylvania. In 1996, she moved to UCLA were she directs the APDA Advanced Center for Parkinson’s Disease Research, the NINDS-funded UCLA Morris K. Udall Center of Excellence for Parkinson’s Disease Research and the NIEHS-funded Center for Gene Environment in Parkinson’s Disease. Her laboratory conducts research on the molecular mechanisms of disorders of the basal ganglia and new treatments for Parkinson’s disease and Huntington’s disease.</p>
<p><strong><a href="http://www.cleartherapeutics.com/wp-content/gallery/sab/cummings-photo.jpg"><img class="alignleft" style="margin-left: 5px; margin-right: 5px;" title="Jeffrey Cummings" src="../wp-content/gallery/sab/cummings-photo.jpg" alt="Jeffrey L. Cummings" width="69" height="104" /></a></strong><strong>Jeffrey L. Cummings, MD</strong> is the director of the Mary S. Easton Center for Alzheimer’s Disease Research at UCLA. The Center has an active drug discovery, drug development and clinical trials program and fosters imaging, genetics, clinical and neuroscience research.  Dr. Cummings also directs the Deane F. Johnson Center for Neurotherapeutics (JCNT) at UCLA.  This unique enterprise supports clinical trials across CNS diseases and provides education and training programs for academicians and pharmaceutical personnel.  Dr. Cummings’ research and leadership contributions in the field of Alzheimer’s disease have been recognized through the Henderson Award of the American Geriatrics Society (2006), the Research Award of the John Douglas French Alzheimer’s Research Foundation (2008), and the Ronald and Nancy Reagan Research Award of the national Alzheimer’s Association (2008). In 2010, he received the Legacy Award from the Ticki Wilkerson-Kassel Movement Therapy Foundation and was honored by the American Association of Geriatric Psychiatry with their Distinguished Scientist Award.</p>
<p><a href="http://www.cleartherapeutics.com/wp-content/gallery/sab/090811-ace-dhobbs-002s.jpg"><img class="alignleft" style="margin-left: 5px; margin-right: 5px;" title="Douglas Hobbs" src="../wp-content/gallery/sab/090811-ace-dhobbs-002s.jpg" alt="Doug Hobbs" width="69" height="103.5" /></a><strong>Doug W. Hobbs, PhD</strong> received his Bachelors degree from the University of California in Santa Cruz in 1984, followed by his Ph.D. from Columbia University in 1989.  After working at Merck Research Laboratories for five years on the development of peptidomimetics for use as hormone antagonists, he joined Pharmacopeia Inc., where as Executive Director of Chemistry he focused on emerging technologies, such as combinatorial chemistry and ultra high-throughput screening, and the integration of those approaches with lead optimization programs.  His efforts contributed to the introduction of several compounds to the clinic, in diverse therapeutic areas including oncology, metabolic disease, cognitive disorders, immunology, and infectious diseases.  After leaving Pharmacopeia in 2006, he directed his efforts at consulting, and teaching at various universities, including the Washington University School of Medicine, where he was a research faculty member in the department of Biochemistry and Molecular Biophysics.</p>
<p><strong><a href="http://www.cleartherapeutics.com/wp-content/gallery/sab/elizabeth-06-e.jpg"><img class="alignleft" style="margin-left: 5px; margin-right: 5px; border: 0px initial initial;" title="Elizabeth Vadas" src="../wp-content/gallery/sab/elizabeth-06-e.jpg" alt="Elizabeth Vadas" width="69" height="86" /></a></strong><strong>Elizabeth B. Vadas, PhD <span style="font-weight: normal;">received her Ph.D. in Physical Chemistry from McGill University in Montreal. She obtained her undergraduate degree in colloid and surface chemistry in Budapest, Hungary. She joined Merck Frosst, the Canadian subsidiary of Merck &amp; Co. in 1980 as a senior research scientist in the department of Pharmaceutical Research and Development.  From 1991 to 2002 Dr. Vadas was head of Pharmaceutical Research and Development at Merck Frosst The department, under her leadership, was responsible from early compound characterization to formulation and process development of new chemical entities including the supply of clinical trial materials from phase I through phase III as well as technical transfer from research to manufacturing.  Notable accomplishments of her department were several products developed in the leukotriene and Cox-2 programs for worldwide introduction. One of the most important of these products from the leukotriene program, leading to worldwide regulatory approval, was SINGULAIR®, Merck’s once a day oral asthma therapy for both adult and pediatric patients.</span></strong></p>
<p><strong><span style="font-weight: normal;"><a href="http://www.cleartherapeutics.com/wp-content/gallery/sab/janet-pic.jpg"><img class="alignleft" style="margin-left: 5px; margin-right: 5px;" title="Janet Wolfe" src="../wp-content/gallery/sab/janet-pic.jpg" alt="Janet Wolfe" width="69" height="104" /></a><strong>Janet Wolfe, PhD</strong> is President and Founder of Wolfe Laboratories (WLI), a biopharmaceutical development services company located in Watertown, Massachusetts.  Dr. Wolfe’s scientific and business career has focused on the intersection of the critical path activities in CMC, DMPK, preclinical and clinical development.  Hundreds of pharmaceutical and biotechnology companies seek the expertise of WLI’s scientific team to facilitate the translation of their compounds from late-stage discovery into the clinic.  Dr. Wolfe has designed and directed early stage development programs for small molecules and biologics across therapeutic areas such as CNS, cardiovascular, metabolic diseases, immunology, and oncology.  WLI has contributed to the advancement of molecules through all stages of development and commercialization. Prior to starting Wolfe Laboratories in 1999, Dr. Wolfe was on the faculty of the Department of Pharmaceutical Sciences at the University of Tennessee, Memphis, which followed her postdoctoral fellowship in the Warren G. Magnuson Clinical Center Pharmacy at the National Institutes of Health.  Dr. Wolfe has over fifteen years experience in pharmaceutical research and development and is the author of numerous articles and presentations.  She has mentored undergraduate and graduate students and postdoctoral fellows over the course of her career.  Dr. Wolfe received her bachelor of science from the University of Sciences in Philadelphia and doctorate in pharmaceutical chemistry from the University of Kansas.</span></strong></p>
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		<title>Clear Therapeutics, Inc. Founding Team</title>
		<link>http://www.cleartherapeutics.com/clear-therapeutics-inc-founding-team</link>
		<comments>http://www.cleartherapeutics.com/clear-therapeutics-inc-founding-team#comments</comments>
		<pubDate>Mon, 29 Mar 2010 18:34:49 +0000</pubDate>
		<dc:creator>Clear</dc:creator>
				<category><![CDATA[Founding Team]]></category>

		<guid isPermaLink="false">http://www.cleartherapeutics.com/?p=62</guid>
		<description><![CDATA[Nolan Sigal, MD PhD — Founder, President. Dr. Sigal, a serial entrepreneur, has spent over 25 years in the academic, pharmaceutical and biotechnology communities. His biotechnology experience includes President of Trellis Bioscience, Inc., Executive Vice President, Research and Development, and CSO at Cytokinetics, Inc. (CYTK) and Senior Vice President, Drug Discovery for Pharmacopeia, Inc. (PCOP), [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://www.cleartherapeutics.com/wp-content/gallery/founders/nolansigal2.jpg"><img class="size-full wp-image-66 alignleft" style="margin-left: 5px; margin-right: 5px;" title="Nolan Sigal" src="http://www.cleartherapeutics.com/wp-content/gallery/founders/nolansigal2.jpg" alt="Nolan Sigal" width="69" height="85" /></a>Nolan Sigal, MD PhD — Founder, President.</strong> Dr. Sigal, a serial entrepreneur, has spent over 25 years in the academic, pharmaceutical and biotechnology communities. His biotechnology experience includes President of Trellis Bioscience, Inc., Executive Vice President, Research and Development, and CSO at Cytokinetics, Inc. (CYTK) and Senior Vice President, Drug Discovery for Pharmacopeia, Inc. (PCOP), where he was one of Pharmacopeia’s founders. Prior to joining Pharmacopeia, Dr. Sigal held several management positions during a 10 year period with Merck &amp; Company Inc, including Executive Director of Immunology Research. Following completion of an M.D./Ph.D. program at the University of Pennsylvania and a pediatric residency, Dr. Sigal was on the faculty at the University of Toronto before moving to Merck.</p>
<p><strong><a href="http://www.cleartherapeutics.com/wp-content/gallery/founders/dsc_0179s.jpg"><img class="alignleft" style="margin-left: 5px; margin-right: 5px;" title="photo-placeholder" src="../wp-content/gallery/founders/dsc_0179s.jpg" alt="photo-placeholder" width="69" height="104" /></a></strong><strong><strong>G</strong>al Bitan, PhD — Founder, Acting CSO.</strong> Dr. Bitan did his graduate studies in organic chemistry at the Hebrew University of Jerusalem, Israel, on unnatural amino acids and non-conventional peptide cyclization. His patented inventions provided the core technology of Peptor, Inc. Dr. Bitan did postdoctoral studies on the structural biology of ligand-receptor systems at Beth Israel-Deaconess Medical Center/Harvard Medical School and continued to tackling the problem of protein misfolding and aggregation at Brigham and Women&#8217;s Hospital/Harvard Medical School. Dr. Bitan has made fundamental contributions to the study of early events in the pathologic cascades that cause Alzheimer&#8217;s disease introducing the use of novel photochemical protein cross-linking techniques for investigation of amyloid ß-protein assembly and discovered one of the earliest oligomers in the assembly cascade, the paranucleus. In 2004, Dr. Bitan joined UCLA where he is currently an Associate Professor of Neurology in the David Geffen School of Medicine.</p>
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		<title>Contact Clear Therapeutics, Inc.</title>
		<link>http://www.cleartherapeutics.com/contact-clear-therapeutics-inc</link>
		<comments>http://www.cleartherapeutics.com/contact-clear-therapeutics-inc#comments</comments>
		<pubDate>Wed, 17 Feb 2010 22:42:56 +0000</pubDate>
		<dc:creator>Clear</dc:creator>
				<category><![CDATA[Contact Us]]></category>

		<guid isPermaLink="false">http://cleartherapeutics.com/?p=17</guid>
		<description><![CDATA[For further information about Clear Therapeutics, Inc. please contact:



General Inquiries
info@ClearTherapeutics.com 






Investor and Media Relations
SaritLevi@ClearTherapeutics.com 






Licensing and  Partnerships
NolanSigal@ClearTherapeutics.com 

























]]></description>
			<content:encoded><![CDATA[<p>For further information about Clear Therapeutics, Inc. please contact:</p>
<table border="0" cellspacing="2" cellpadding="0" width="429">
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<td><span><strong>General Inquiries</strong></span></td>
<td><span><a title="mailto:info@ClearTherapeutics.com CTRL + Click to follow link" onmouseover="this.className='navcont_on';" onmouseout="this.className='navcont_off'" href="mailto:info@ClearTherapeutics.com">info@ClearTherapeutics.com </a></span></td>
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<td><span><strong>Investor and Media Relations</strong></span></td>
<td><span><a title="mailto:SaritLevi@ClearTherapeutics.com CTRL + Click to follow link" onmouseover="this.className='navcont_on';" onmouseout="this.className='navcont_off'" href="mailto:SaritLevi@ClearTherapeutics.com">SaritLevi@ClearTherapeutics.com </a></span></td>
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<td><span><strong>Licensing and  Partnerships</strong></span></td>
<td><span><a title="mailto:NolanSigal@starpharma.com CTRL + Click to follow link" onmouseover="this.className='navcont_on';" onmouseout="this.className='navcont_off'" href="mailto:NolanSigal@starpharma.com">NolanSigal@ClearTherapeutics.com </a></span></td>
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		<title>The Clear Approach</title>
		<link>http://www.cleartherapeutics.com/the-clear-approach</link>
		<comments>http://www.cleartherapeutics.com/the-clear-approach#comments</comments>
		<pubDate>Wed, 17 Feb 2010 22:04:08 +0000</pubDate>
		<dc:creator>Clear</dc:creator>
				<category><![CDATA[Our Approach]]></category>

		<guid isPermaLink="false">http://cleartherapeutics.com/?p=10</guid>
		<description><![CDATA[ 
 
 
Current Status of Care
 
Currently, there are five FDA-approved drugs for Alzheimer’s disease (AD),  all of which treat the symptoms, but not the cause of the disease. The  beneficial effects of these drugs are mild and temporary.
 
Parkinson’s disease (PD) patients currently are treated mainly by  dopamine-replacement therapy, which [...]]]></description>
			<content:encoded><![CDATA[<p><strong><span style="font-family: GillSans-Bold; color: #343434;"><span style="font-family: GillSans-Bold; color: #343434;"> </span></span></strong></p>
<p><span style="font-family: TimesNewRomanPSMT; color: #343434;"><span style="font-family: TimesNewRomanPSMT; color: #343434;"><strong><span style="font-family: GillSans-Bold; color: #343434;"><span style="font-family: GillSans-Bold; color: #343434;"> </span></span></strong></span></span></p>
<p><strong> </strong></p>
<div><strong>Current Status of Care</strong></div>
<p><strong> </strong></p>
<div>Currently, there are five FDA-approved drugs for Alzheimer’s disease (AD),  all of which treat the symptoms, but not the cause of the disease. The  beneficial effects of these drugs are mild and temporary.</div>
<p><strong> </strong></p>
<div>Parkinson’s disease (PD) patients currently are treated mainly by  dopamine-replacement therapy, which initially is effective in treating the major  symptoms – tremor and rigidity, but the effects wear off after a while.  Unfortunately, the treatment causes major side effects, such as involuntary  movement, which may become more debilitating than the disease itself. In  addition, because it does not treat the cause of the disease,  dopamine-replacement therapy has no effect on “non-dopaminergic” symptoms of PD,  including falling, freezing, insomnia, chronic constipation, loss of sense of  smell, depression, and dementia, each which afflicts a large percentage of  people with the disease.</div>
<p><strong> </strong></p>
<div><strong>The Problem: A Major Public Health Challenge</strong></div>
<p><strong> </strong></p>
<div>Alzheimer’s and Parkinson’s diseases are the two most prevalent  neurodegenerative diseases, together affecting over 55 millions of people  worldwide. Due to the rapid aging of the population, both diseases threaten to  become epidemics in the 21st century. The life span of patients with AD is 8  years on average and may extend up to 20 years from the onset of symptoms.  During the long years of illness, the patients, families, caretakers, and  society in general suffer grave emotional and financial duress.</div>
<p><strong> </strong></p>
<div><strong>Alzheimer’s statistics:</strong> Current cost estimates of care for patients  with AD in the US are ~$150 billion a year. More than 35 million people  worldwide have AD. This number is projected to nearly double every 20 years, to  66 million in 2030, and 115 million in 2050.</div>
<p><strong> </strong></p>
<div><strong>Parkinson’s statistics:</strong> Current global estimates of PD are 22 million.  Similar to AD, the major risk factor for PD is age. However, unlike AD, which  very rarely afflicts people under age 60, PD strikes people in their 20’s and  30’s who struggle to work and raise families.</div>
<p><strong> </strong></p>
<div><strong>Common pathologic mechanism:</strong> Both AD and PD are caused by abnormal  protein aggregation and both diseases have no cure. In each disease, the natural  control systems of the brain fail to manage a particular protein. The protein  then self-associates into toxic aggregates that disrupt the normal function of  brain cells and eventually and kill them. Treatment and prevention of these  diseases is a major, unmet, public health challenge.</div>
<p><strong> </strong></p>
<div><strong>The Solution: Rational Drug Design</strong></div>
<p><strong> </strong></p>
<div>Our solution is a unique, rational approach to drug design. Using this  approach, Clear Therapeutics has discovered novel compounds that block the  self-association of the proteins that cause AD and PD and rescue the normal  function of brain cells. Initial preclinical experiments show high efficacy in  animal models without signs of negative side effects.</div>
<p><strong> </strong></p>
<div><strong>The unique Clear approach:</strong> Traditional drug discovery is based on  high-throughput screening of thousands-to-millions of compounds. Despite  tremendous efforts, this approach has not been successful for AD and PD because  aggregated proteins are very different from traditional drug targets.</div>
<p><strong> </strong></p>
<div>Clear’s discoveries are the result of a rational design paradigm developed  by Dr. Gal Bitan in the Department of Neurology at UCLA. Since 1999, Dr. Bitan  has been studying a protein called beta-amyloid, which self-associates into  neurotoxic aggregates in the brain and causes AD. Dr. Bitan used his intimate,  detailed knowledge of the molecular interactions that control beta-amyloid  aggregation to discover novel compounds that act through a unique, proprietary  mechanism and do not suffer from the shortcomings and side effects that have  plagued competing approaches.</div>
<p><strong> </strong></p>
<div>The unique mechanism by which the compounds discovered by Dr. Bitan work  enables targeting not only beta-amyloid, but also a variety of proteins that  self-associate into toxic aggregates and cause more than 30 different diseases,  commonly called “amyloidoses,” including Parkinson’s disease, dialysis-related  amyloidosis, type 2 diabetes, systemic amyloidosis, and others.</div>
<div>Clear has licensed the technology from UCLA and is developing novel  therapeutics for Alzheimer’s disease, Parkinson’s disease, and other  amyloidoses.</div>
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