The day will start with registration from 1:30 p.m. CEST. The program starts at 2:00 p.m. CEST and ends with refreshments and mingle at 5:00 p.m. CEST. The Capital Markets Day will take place at the IVA Conference Center’s Wallenberg Hall at Grev Turegatan 16 in Stockholm.
2:00 p.m Welcome by Moderator Lars Frick and CEO Erik Kinnman.
2:05 p.m Magnus Persson – Associate Professor in physiology, private equity investor and Director of the Board – gives his view of why investments in pharmaceutical development within rare diseases are highly interesting.
2:30 p.m Dr Amel Karaa – Massachusetts General Hospital – international expert in primary mitochondrial diseases, describes the unmet medical need and the research development within the field.
3:00 p.m CEO Erik Kinnman presents NeuroVive’s updated strategy, the portfolio, and describes the background.
3:30 p.m Coffee break: Take the opportunity to ask questions.
4:00 p.m CMO Magnus Hansson and CSO Eskil Elmér give a closer description of the company’s central projects and the external collaborations.
4:30 p.m Matilda Hugerth – Director Clinical & Regulatory Affairs – describes orphan drugs and their regulatory path to market.
5:00 p.m Conclusions followed by mingle and refreshments.
The Capital Markets Day will be moderated by Lars Frick of the equities publication Börsveckan. The written presentations will be in English, and the lectures will mainly be held in Swedish.
The program will be available on NeuroVive’s website after the event. There will also be a live webcast via https://tv.streamfabriken.com/neurovive-cmd-2019.
The information was submitted for publication, through the agency of the contact person set out below, at 08:30 a.m. CEST on 9 October 2019.
For more information please contact:
Catharina Johansson, CFO, IR & Communications
+46 (0)46-275 62 21, firstname.lastname@example.org
NeuroVive Pharmaceutical AB (publ)
Medicon Village, SE-223 81 Lund, Sweden
Tel: +46 (0)46 275 62 20 (switchboard)
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NeuroVive Pharmaceutical AB is a leader in mitochondrial medicine, with one project in clinical phase I (KL1333) for chronic treatment of primary mitochondrial diseases and one project, in preparation for clinical trials (NV354), for treatment of primary mitochondrial diseases with Complex I deficiency. NeuroSTAT for traumatic brain injury is another clinical phase project. The R&D portfolio also consists of projects for mitochondrial myopathy, NASH and cancer. NeuroVive’s ambition is to take drugs for rare diseases through clinical development and all the way to market, with or without partners. For projects for common indications the goal is out-licensing in preclinical phase. A subset of compounds under NeuroVive’s NVP015 program has been licensed to Fortify Therapeutics, a BridgeBio company, for the development of a local treatment of Leber’s Hereditary Optic Neuropathy (LHON). NeuroVive is listed on Nasdaq Stockholm, Sweden (ticker: NVP). The share is also traded on the OTCQX Best Market in the US (OTC: NEVPF).