Report

Outlook: Cough cold portfolio gathers momentum

The Tuzistra XR FDA filing is an important step towards Vernalis’s goal of profitable sustainability. Potential approval (assuming NDA acceptance in mid-September) and launch within the next 12 months, into the 2015/16 winter cough cold season, suggest first US cough cold revenues are possible in H215. The four other US cough cold prescription-only extended release products should also achieve development and regulatory milestones in the intervening period. These milestones will be the focus of investors given they will confirm the de-risking of this portfolio, triggering potential upgrades to our current £240m (54p/share) rNPV-based valuation.
Underlying
Vernalis PLC

Vernalis is a holding company. Through its subsidiaries, Co. is a commercial stage pharmaceutical company focused on drug development. Co. has three marketed products: Tuzistra® XR, in the U.S. prescription cough cold market; Moxatag®, the only once-daily amoxicillin approved in the U.S. for tonsillitis and pharyngitis; and frovatriptan, an acute treatment for migraine. In addition, Co.'s nine programs in its new chemical entity development pipeline are: V158866 for central nervous system indications; CP1-444 and V2006 for immuno-oncology indications; AUY922, Tosedostat, Bcl-2, Mcl-1, and V158411 for cancer indications; and RPL554 for chronic obstructive pulmonary disease indications.

Provider
Edison Investment Research
Edison Investment Research

Edison is an investment research and advisory company, with offices in North America, Europe, the Middle East and AsiaPac. The heart of Edison is our world renowned equity research platform and deep multi-sector expertise. At Edison Investment Research, our research is widely read by international investors, advisors and stakeholders. Edison Advisors leverages our core research platform to provide differentiated services including investor relations and strategic consulting.

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