A innovator in the field of regenerative medicine.

These trials are prospective, open-label studies, made to determine the security and tolerability of hESC-derived RPE cells following sub-retinal transplantation into patients with dry-AMD or Stargardt’s macular dystrophy at 12 months, the study’s primary endpoint. Preliminary results relating to both early protection and biological function for the first two individuals in america, one SMD patient and one dried out AMD patient, were recently reported in The Lancet. On January 20, 2012, the first SMD patient to be enrolled in the business’s U.K. Clinical trial was treated at Moorfields Eye Hospital in London. The ultimate patient of the initial cohort in the company’s SMD trial in the U.S.This all-share contract demonstrates our confidence in AAA's long term strategy and we are delighted to really have the opportunity to be considered a right part of this.’Â Â.

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