Daily dose of Aubagio reduces rate of relapse
* Shares down 1.2 pct in line with CAC 40
PARIS, June 1 (Reuters) – Sanofi reported positive results from a late-stage trial of its Aubagio multiple sclerosis drug, bolstering its chances of approval by regulators as it seeks to catch up with a fast-selling oral treatment from rival Novartis.
Sanofi said it found that a daily dose of the treatment, one of two multiple sclerosis drugs it has in late-stage development, reduced the rate of relapse by 36 percent compared with a placebo.
The study assessed the efficiency and safety of Aubagio in 1,169 patients with relapsing forms of multiple sclerosis.
The full data from the study will be presented at an upcoming scientific meeting, Sanofi said.
Cheuvreux analyst Marcel Brand, who has an “outperform” recommendation on Sanofi stock, said the results were positive and consistent with earlier data, “which is reassuring”.
Brand expects Aubagio to generate peak sales of $1.8 billion in 2018, taking around 11 percent of volume market share.
The FDA’s response is due by July 2012, while EMA is expected to give its feedback in the first quarter of 2013.
Compared with older therapies, Aubagio has the advantage of being an oral drug.
But it has produced less impressive results in clinical tests than other oral MS treatments and has failed to show it was better than a commonly used injectable drug for MS, although it did have milder side effects.
Analysts expect the drug could find a niche among newly diagnosed patients, since around 35 to 40 percent of MS patients prefer to take no medication rather than face unwanted side effects.
MS, which has no cure, affects 2.5 million people worldwide. It is a chronic, often disabling disease that attacks the central nervous system and can lead to numbness, paralysis and loss of vision.
Sanofi shares, which have declined around 3.5 percent since the start of the year, were trading 1.2 percent lower at 54.34 euros at 0935 GMT, matching a fall in the CAC 40 index.