MARLBOROUGH, Mass.--(BUSINESS WIRE)--  
    Advanced Cell Technology, Inc. (ACT; OTCBB: ACTC), a leader    in the field of regenerative medicine, today announced    treatment of the fourth patient, the first in the second    patient cohort, in the companys Phase I/II clinical trial for    dry age-related macular degeneration (dry AMD) using retinal    pigment epithelial (RPE) cells derived from human embryonic    stem cells (hESCs). The surgery was performed on Wednesday,    Aug. 1 atWills    Eye Institutein Philadelphia, by a surgical team lead    by     Carl D. Regillo, M.D., Chief of the Wills Eye Institute    Retina Service, and professor of ophthalmology at Thomas    Jefferson University. The patient was injected with 100,000    hESC-derived RPE cells and is recovering uneventfully.  
    We are very pleased to have the second dose cohort in both of    our U.S. clinical trials underway, commented Gary Rabin,    chairman and CEO of ACT. We are encouraged by our ongoing    progress in all three of our clinical trials using our    hESC-derived RPE cells to treat forms of macular degeneration.    We have not observed any complications or side effects from the    stem cell-derived RPE cells, and we will continue to monitor    the patients for safety, tolerability and efficacy of this    therapy.  
    The dry AMD trial is one of three clinical trials being carried    out by the company in the U.S. and in Europe. Each trial will    enroll 12 patients, with cohorts of three patients in an    ascending dosage format. These trials are prospective,    open-label studies, designed to determine the safety and    tolerability of hESC-derived RPE cells following sub-retinal    transplantation into patients with dry AMD or Stargardt's    macular dystrophy (SMD) at 12 months, the studys primary    endpoint. Preliminary results from the two U.S. trials were        reported in     The Lancet earlier this year.  
    Doubling the cell dosage in both our U.S. trials is an    important step forward in our clinical programs, said Robert    Lanza, M.D., ACTs chief scientific officer. We anticipate    continued progress and safety findings in both our U.S. trials    as well as our concurrent European trial.  
    Dry AMD is the most common cause of vision loss in patients    over 50 years and affects around 30 million people worldwide,    said Dr. Regillo. Dry AMD is a form of macular degeneration    with no approved drug treatment available to date. ACTs    hESC-derived RPE cells could address the unmet medical need of    combating dry AMD and other macular degenerations such as    Stargardts disease. We are looking forward to analyzing the    safety and efficacy data.  
    Further information about patient eligibility for ACTs dry AMD    study and the concurrent studies in the U.S. and the E.U. for    SMD is available atwww.clinicaltrials.gov,with    the following Identifiers: NCT01344993 (dry AMD), NCT01345006    (U.S. SMD), and NCT01469832 (E.U. SMD).  
    About dry AMD  
    Degenerative diseases of the retina are among the most common    causes of untreatable blindness in the world. Age-related    macular degeneration (AMD) is the leading cause of blindness in    people over age 60 in the United States, and the vast majority    of cases of AMD are of the dry form, which is currently    untreatable.  
    About Advanced Cell Technology, Inc.  
Excerpt from:
ACT Announces First Dry AMD Patient Treated with Higher Dosage of Embryonic Stem Cell-Derived RPE Cells