Announces open enrollment of highest dose cohort after safety review

LOS ALTOS, CA, February 19, 2016 – Retrotope announced today the successful completion of the first dose cohort and the opening of patient enrollment for the highest dose cohort in its ongoing 28-day study of orally dosed RT001 in Friedreich’s ataxia (FA) patients. RT001 was well tolerated and no serious adverse events or dose limiting toxicities were observed.

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