To my knowledge all patients ACT has treated to date for SMD/AMD trials are on the immunosuppression regimen. ACT has no trial for hemangioblast at this time so I am not sure what that has to do with current trials underway?
Here is a clip from the Lancet Publication on ACT's first two patients..
" The immunosuppression regimen included low-dose tacrolimus (target blood concentrations 3–7 ng/mL) and mycophenolate mofetil (ranging from 0·25 to 2·00 g orally per day) a week before the surgical procedure and continued for 6 weeks. At week 6, the regimen calls for discontinuation of tacrolimus and a continuation of mycophenolate mofetil for an additional 6 weeks." http://download.thelancet.com/flatcontentassets/pdfs/S0140673612600282.pdf
A recent article on the UK patient, Marcus Hilton,
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