Capnia Joins the Consortium for Universal Rh Disease Elimination (CURhE) as Founding Member

Mar 7, 2016

Coalition seeks to eradicate Rh Disease/HDFN globally

Inaugural meeting to be held today at Stanford University

REDWOOD CITY, Calif., March 07, 2016 (GLOBE NEWSWIRE) -- Capnia, Inc. (NASDAQ:CAPN), a diversified healthcare company that develops and commercializes innovative diagnostics, devices and therapeutics addressing unmet medical needs, today announced that it has joined the Consortium for Universal Rh Disease Elimination (CURhE) as a Founding Member. CURhE is a global consortium that has been established to eradicate Hemolytic Disease of the Fetus and Newborn (HDFN), a potentially fatal disease that is caused by an incompatibility between a mother’s and her baby’s blood due to differing blood proteins called Rh Factors. CURhE estimates that HDFN affects over 300,000 newborns globally every year.

“Rh Disease has been largely eradicated from many parts of the world, and we believe the same is possible in those regions where it continues to pose a threat,” said Anish Bhatnagar, MD, Chief Executive Officer of Capnia. “We are eager to join forces with these leading institutions and apply our expertise in neonatology to help raise awareness and funding to combat a disease that is easily preventable. Detecting hemolysis is an important part of the CURhE strategy to eliminate Rh Disease. Our ETCO monitor, as the only point of care device available to do so in neonates, can play an important role in the identification of hemolysis in babies and therefore lead to earlier treatment based on AAP Guidelines.”   

At CURhE’s inaugural planning meeting, which is being held today at Stanford University, the founding members of the Consortium are gathering to formulate a global strategic plan, outline tactics and develop fund-raising activities. Pediatricians and neonatologists from 16 countries around the world will be joining the meeting together with International Federation of Obstetric and Gynecologists and the International Pediatric Association.

Among CURhE’s other founding members are the Stanford University School of Medicine, the Hospital for Sick Children in Toronto, Canada, Siena University in Siena, Italy, and two other companies in the medical field: Kedrion Biopharma, based in Lucca, Italy, which produces the most widely known preventative treatment for HDFN, and Eldon Biologicals, a Danish company that produces a quick and simple method to determine Rh blood group.

About HDFN/Rh Disease
HDFN or Rh disease is the result of a mismatch between a pregnant woman’s blood and that of her developing fetus. One characteristic of a person’s blood is whether it has a protein called an Rh Factor. If you have this protein – and most people do – your blood is called “Rh Positive.” People whose blood does not have this protein are said to be “Rh Negative.” For the most part people with Rh Negative blood suffer no ill consequences – many people never know their Rh type. But if a woman who is Rh Negative is pregnant with an Rh Positive fetus (as a result of having an Rh Positive father), the baby - and especially subsequent pregnancies – could be in great danger because the mother’s blood type is not compatible with the baby’s blood type.  Due to this incompatibility, the mother’s immune system attacks and destroys the fetus’ or baby’s red blood cells.  As a result, the fetus may die in the womb or the newborn may die or have brain damage. A severe form of brain damage called kernicterus may occur due to bilirubin build up in the baby’s body and deposition in the brain.  The manifestations are varied, and may include cerebral palsy, hearing, visual impairment, digestive, sleeping and dental problems. 

About Capnia
Capnia, Inc. is a diversified healthcare company that develops and commercializes innovative diagnostics, devices and therapeutics addressing unmet medical needs. Capnia's lead commercial product, CoSense®, is based on the Sensalyze™ Technology Platform. It is a portable, non-invasive device that rapidly and accurately measures carbon monoxide (CO) in exhaled breath. CoSense has 510(k) clearance for sale in the U.S. and has received CE Mark certification for sale in the European Union. CoSense is used for the monitoring of CO from internal sources (such as hemolysis, a dangerous condition in which red blood cells degrade rapidly), as well as external sources (such as CO poisoning and smoke inhalation). The initial target market is newborns with jaundice that are at risk for hemolysis, comprising approximately three million births in the U.S. and European Union. CoSense may play an important role in detecting the rate of hemolysis that occurs in newborns with Rh disease.  The Company's commercial, neonatology-focused product line also includes innovative pulmonary resuscitation solutions, including the NeoPIP™ Infant T-Piece Resuscitator and Universal T-Piece Circuit consumables. Capnia's proprietary therapeutic technology uses nasal, non-inhaled CO2 and is being evaluated to treat the symptoms of allergies, as well as the trigeminally-mediated pain conditions such as cluster headache, trigeminal neuralgia and migraine.

Forward-Looking Statements
This press release contains forward-looking statements that are subject to many risks and uncertainties. Forward-looking statements include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things, our ongoing and planned product development, renewed focus on our therapeutic business and our ability to report data from our TN Pilot clinical trial in 2016.

We may use terms such as "believes," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should," "approximately" or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. Although we believe that we have a reasonable basis for each forward-looking statement contained herein, we caution you that forward-looking statements are not guarantees of future performance and that our actual results of operations, financial condition and liquidity, and the development of the industry in which we operate may differ materially from the forward-looking statements contained in this presentation. As a result of these factors, we cannot assure you that the forward-looking statements in this presentation will prove to be accurate. Additional factors that could materially affect actual results can be found in Capnia's Form 10-Q filed with the Securities and Exchange Commission on November 12, 2015, including under the caption titled "Risk Factors." Capnia expressly disclaims any intent or obligation to update these forward looking statements, except as required by law.

Investor Relations Contact:
Michelle Carroll/Susie KimArgot Partners
(212) 600-1902
michelle@argotpartners.com
susan@argotpartners.com

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