Emmaus Life Sciences Receives U.A.E. Marketing Authorization for Endari®
On March 23, 2022, Emmaus Life Sciences announced the U.A.E. Ministry of Health approved its marketing application for Endari®, a treatment for sickle cell disease. After a five-month review, Endari was previously available only on an early access basis. Emmaus estimates about 600 sickle cell patients reside in the U.A.E. and approximately 225,000 in the MENA region could benefit from the drug. The company aims to secure further approvals across Gulf Cooperation Council states, highlighting the significance of this market due to the higher prevalence of sickle cell disease compared to the U.S.
- U.A.E. Ministry of Health approved marketing authorization for Endari, expanding its market presence.
- Estimated 600 patients in U.A.E. and 225,000 in MENA could benefit from Endari treatment.
- None.
TORRANCE, Calif., March 23, 2022 /PRNewswire/ -- Emmaus Life Sciences, Inc. (OTCQX: EMMA) a commercial-stage biopharmaceutical company and leader in the treatment of sickle cell disease, today announced the approval of its application for marketing authorization of Endari® from the United Arab Emirates (U.A.E.) Ministry of Health after a five-month review of the company's marketing authorization application. During the review period, Endari was available in the U.A.E. on a named patient, or early access, basis only.
Emmaus estimates that as many as 600 sickle cell disease patients live or work in the U.A.E. and that there are approximately 225,000 sickle cell disease patients throughout the Middle East North Africa (MENA) region who could potentially be treated with Endari.
"We are grateful to have received the Ministry of Health's approval of Endari for the treatment of sickle cell disease patients in the U.A.E. and will move as quickly as possible to reach this population," stated Yutaka Niihara, M.D., M.P.H., Chairman and Chief Executive Officer of Emmaus. "This is the first of several full marketing approvals we hope to obtain in Gulf Cooperation Council states, which represent a very important market, given that there are more than double the number of sickle cell disease patients within these areas than there are in the United States."
George Sekulich, Senior Vice President of Global Commercialization of Emmaus added, "After the extensive review by the Ministry of Health, the approval to market Endari is an important step forward for Emmaus in the MENA region. We look forward to working with our distribution partner to make Endari available to sickle cell disease sufferers in the U.A.E."
About Emmaus Life Sciences
Emmaus Life Sciences, Inc. is a commercial-stage biopharmaceutical company and leader in the treatment of sickle cell disease. The company currently markets U.S. Food and Drug Administration approved Endari® (L-glutamine oral powder) indicated to reduce the acute complications of sickle cell disease in adults and children 5 years and older. The company is also engaged in the discovery and development of innovative treatments and therapies for certain rare and orphan diseases as well as those affecting larger populations, such as diverticulosis. For more information, please visit www.emmausmedical.com.
About Endari® (prescription grade L-glutamine oral powder)
Endari®, Emmaus' prescription grade L-glutamine oral powder, was approved by the FDA in July 2017 for treating sickle cell disease in adult and pediatric patients five years of age and older. Sales of Endari® began in the United States in 2018.
Indication
Endari® is indicated to reduce the acute complications of sickle cell disease in adult and pediatric patients five years of age and older.
Important Safety Information
The most common adverse reactions (incidence >10 percent) in clinical studies were constipation, nausea, headache, abdominal pain, cough, pain in extremities, back pain, and chest pain.
Adverse reactions leading to treatment discontinuation included one case each of hypersplenism, abdominal pain, dyspepsia, burning sensation, and hot flash.
The safety and efficacy of Endari in pediatric patients with sickle cell disease younger than five years of age has not been established.
For more information, please see full Prescribing Information of Endari at: www.ENDARIrx.co/PI.
About Sickle Cell Disease
There are approximately 100,000 people living with sickle cell disease (SCD) in the United States and millions more globally. The sickle gene is found in every ethnic group, not just among those of African descent; and in the United States an estimated 1-in-365 African Americans and 1-in-16,300 Hispanic Americans are born with SCD.1 The genetic mutation responsible for SCD causes an individual's red blood cells to distort into a "C" or a sickle shape, reducing their ability to transport oxygen throughout the body. These sickled red blood cells break down rapidly, become very sticky, and develop a propensity to clump together, which causes them to become stuck and cause damage within blood vessels. The result is reduced blood flow to distal organs, which leads to physical symptoms of incapacitating pain, tissue and organ damage, and early death.2
1Source: Data & Statistics on Sickle Cell Disease – National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, December 2020. |
Forward-looking Statements
This press release contains forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended, including statements regarding potential increased sales of Endari following full marketing authorization for Endari in the U.A.E. and other countries in the Middle East North Africa region. These forward-looking statements are subject to numerous assumptions, risks and uncertainties which change over time, including risks inherent in the regulatory approval process and other factors set forth in the company's Annual Report on Form 10-K/A filed with the Securities and Exchange Commission (SEC) on August 10, 2021, and other SEC reports, and actual results may differ materially. Such forward-looking statements speak only as of the date they are made, and Emmaus assumes no duty to update them, except as may be required by law.
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SOURCE Emmaus Life Sciences, Inc.
FAQ
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