Lund, Sweden, January 3, 2017 - NeuroVive Pharmaceutical AB (Nasdaq Stockholm: NVP, OTCQX: NEVPF), the mitochondrial medicine company, today announces that the company is scheduled to present the 9th Annual Biotech Showcase Conference held January 9-11, 2017 in San Francisco, US. During the presentation, an update regarding NeuroVive’s research and development programs will be provided.
The presentation will include the company’s two orphan drug projects, NeuroSTAT® in clinical phase II for the treatment of traumatic brain injury (TBI), and the discovery project NVP015 targeting genetic mitochondrial diseases. Also, the preclinical out-licensing projects related to the large NASH indication, NV556 and NVP022, will be presented.
The presentation will take place on January 10, at 5:00 p.m. PST /Jan 11 2:00 a.m. CET. The audio and slide presentation will be webcasted live and can be accessed via the NeuroVive web site. To access the live and replay presentations please go to http://www.neurovive.com/en/investor/company-presentations/ .
About NeuroVive
NeuroVive Pharmaceutical AB is a leader in mitochondrial medicine. The company is committed to the discovery and development of medicines that preserve mitochondrial integrity and function in areas of unmet medical need. The company’s strategy is to take drugs for rare diseases through clinical development and into the market. The strategy for projects within larger indications outside the core focus area is out-licensing in the preclinical phase. NeuroVive enhances the value of its projects in an organization that includes strong international partnerships and a network of mitochondrial research institutions, as well as having expertise in drug development and production.
NeuroVive has a project in early clinical phase II development for the prevention of moderate to severe traumatic brain injury (NeuroSTAT®). NeuroSTAT has orphan drug designation in Europe and in the US. The R&D portfolio consists of several late stage research programs in areas ranging from genetic mitochondrial disorders to neurological and metabolic diseases such as NASH.
