SAN RAMON, Calif., May 26, 2017 (GLOBE NEWSWIRE) -- SteadyMed Ltd. (Nasdaq:STDY), a specialty pharmaceutical company focused on the development of drug product candidates to treat orphan and high-value diseases with unmet parenteral delivery needs, today announced that one of its largest institutional shareholders has exercised warrants to purchase additional ordinary shares of the Company received in conjunction with the first tranche of SteadyMed’s third quarter 2016 private placement. As a result of the exercise, SteadyMed has received additional proceeds totaling approximately $5 million.
SteadyMed remains on track to submit a New Drug Application (NDA), for Trevyent®, which is in development for the treatment of Pulmonary Arterial Hypertension (PAH), in the second quarter of 2017.
“This additional capital, which follows the successful completion of a $30 million private placement in April, provides us with greater financial resources as we increase our pre-commercial and manufacturing initiatives to support an impactful launch of Trevyent, subject to FDA approval, in mid-2018,” said Jonathan Rigby, President & CEO of SteadyMed. “These are exciting times for SteadyMed, and the exercise of these warrants represents an important vote of confidence from one of our largest healthcare-focused institutional investors. We are confident that Trevyent, if approved, will take a meaningful share of the PAH market and our growing body of high quality, diligent investors who support our vision, is a testament to that.”
About SteadyMed
SteadyMed Ltd. is a specialty pharmaceutical company focused on the development of drug products to treat orphan and high value diseases with unmet parenteral delivery needs. The company's lead drug product candidate is Trevyent, a development stage drug product that combines SteadyMed's pre-filled, sterile, single use, disposable, PatchPump® infusion system, with treprostinil, a vasodilatory prostacyclin analogue to treat pulmonary arterial hypertension (PAH). SteadyMed intends to commercialize Trevyent in the U.S. and has signed an exclusive license and supply agreement with Cardiome Pharma Corp. for the commercialization of Trevyent in Europe, Canada and the Middle East. SteadyMed has offices in San Ramon, California and Rehovot, Israel. For additional information about SteadyMed please visit www.steadymed.com.
Forward Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include, among others, statements about the company's ability to advance its development-stage product candidates, including Trevyent. Forward-looking statements reflect the company's current views with respect to certain current and future events and are subject to various risks, uncertainties and assumptions that could cause actual results to differ materially. Risks and uncertainties include, but are not limited to, the risk that Trevyent does not demonstrate clinical superiority to existing parenteral treprostinil products, that Trevyent is not approved for commercialization by the FDA or approval is delayed by patent litigation, that Trevyent is not granted orphan drug exclusivity, the risk that drug development involves a lengthy and expensive process with uncertain outcome, that the company will not satisfy the milestone and other closing conditions to call the second tranche of its July 2016 private placement, that the company will continue to need additional funding, and that the company may be unable to raise capital when needed, which would force the company to delay, reduce or eliminate its product candidate development programs and potentially cease operations. There can be no assurance that the company will be able to complete the offering on the terms described herein or in a timely manner, if at all. The risks, uncertainties and assumptions referred to above are discussed in detail in our reports filed with the Securities and Exchange Commission, including our Quarterly Report on Form 10-Q filed on May 12, 2017. The company does not undertake to publicly update or revise any forward-looking statements to reflect events or circumstances that may arise after the date hereof except as may be required by law.