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Vernalis awaits FDA decision

Vernalis has changed its financial year-end as it waits for US regulators to approve a new product
February 10, 2015

Vernalis (VER) chief executive Ian Garland warned last summer that the Aim-traded biotech outfit's financial results would be "lumpy" until the launch of Tuzistra, a new slow-release cold and cough product, in mid-2015. And so it has turned out: in 2014 royalty income from migraine treatment Frovatriptan dipped to £1.7m (from £4.1m in the second half of 2013), while income from research collaborations jumped to £3.8m (from £2.3m in the second half of 2013). Overall, group sales fell 16 per cent.

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The US Food and Drug Administration (FDA) should give Tuzistra the go-ahead in April, but Vernalis is also working on four other cough and cold programmes in the meantime. Mr Garland said investors could receive "up to 10 updates" on these new drugs over the next 12 to 18 months.

Vernalis has changed its financial year to better coincide with the US cough and cold season. Mr Garland says the season runs roughly between October and March, so a December year-end split the key trading period in two. Analysts at broker N+1 Singer expect losses of £16.4m for the 18 months to 30 June - the new financial year-end - giving losses per share of 3.2p.

VERNALIS (VER)
ORD PRICE:50pMARKET VALUE:£221m
TOUCH:49-51p12-MONTH HIGH:53pLOW: 29p
DIVIDEND YIELD:nilPE RATIO:na
NET ASSET VALUE:18pNET CASH:£71m

Year to 31 DecemberTurnover (£m)Pre-tax profit (£m)Earnings per share (p)Dividend per share (p)
201014.2-22.1-21.1nil
201112.2-10.6-8.9nil
201214.6-6.8-1.4nil
201314.1-6.3-0.9nil
201411.9-5.2-0.7nil
% change-16---

Ex-div: na

Payment: na