CorMedix Inc. to Present at 2016 Rodman & Renshaw 18th Annual Global Investment Conference
BEDMINSTER, NJ / ACCESSWIRE / September 6, 2016 / CorMedix Inc. (NYSE MKT: CRMD), a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory diseases, announced today that chief executive officer Randy Milby will present at the 2016 Rodman & Renshaw 18th Annual Global Investment Conference, to be held September 11-13, 2016, at the Lotte New York Palace Hotel in New York City.
Milby will provide an overview of the company's business during a live presentation, and will be available to participate in one-on-one meetings with investors who are registered to attend the conference.
CorMedix's presentation is scheduled for 9:10 a.m. Eastern Time on Monday, September 12, 2016. A live webcast of the presentation will be available on CorMedix's Investors web page: http://www.cormedix.com/#!investors/cldq
About CorMedix Inc.
CorMedix Inc. is a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory disease. The Company is focused on developing its lead product Neutrolin®, a novel, non-antibiotic antimicrobial solution designed to prevent costly and dangerous bloodstream infections associated with the use of central venous catheters. Such infections cost the U.S. healthcare system approximately $6 billion annually and contribute significantly to increased morbidity and mortality. Neutrolin is currently in a Phase 3 clinical study in patients undergoing chronic hemodialysis via a central venous catheter. The company is planning to conduct its second Phase 3 study in patients with cancer receiving IV parenteral nutrition, chemotherapy and hydration via a chronic central venous catheter, subject to sufficient resources. If successful, the two pivotal studies may be submitted to the FDA for potential approval for both patient populations. Neutrolin has FDA Fast Track status and is designated as a Qualified Infectious Disease Product, contributing to potentially accelerated FDA review and up to 10 years of market exclusivity upon potential U.S. approval. It is already a CE Marked product in Europe and other territories. CorMedix is also seeking to unlock additional value for its taurolidine-based technology by establishing collaborative partnerships in oncology and medical device applications. For more information visit: www.cormedix.com.
For Investors & Media:
Tiberend Strategic Advisors, Inc.
Joshua Drumm, Ph.D.: jdrumm@tiberend.com; (212) 375-2664
Janine McCargo: jmccargo@tiberend.com; (646) 604-5150
SOURCE: CorMedix Inc.
