News that two-year follow-up data from a small Phase I study
showed improvements in limb function with no worrying safety
issues lifted shares in ReNeuron 10 percent by 0830 EDT.
The clinical results were presented at the European Stroke
Organisation Conference in Glasgow.
The company said there had been no cell-related or immunological
adverse events in any of the 11 patients treated. The only
problems seen were related only to the implantation procedure or
the patient's underlying medical condition.
Improvements in neurological status and limb function were
observed within three months of treatment and maintained
throughout long-term follow-up.
The procedure involves injecting ReNeuron's neural stem cells
into patients' brains to repair areas damaged by stroke, thereby
improving both mental and physical function.
The Phase I trial is designed primarily to test whether the
experimental treatment is safe.
(Reporting by Ben Hirschler; editing by Jason Neely)
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