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CPCB-RPE1 for Macular Degeneration
Study Summary
This trial is designed to assess the feasibility of delivery and safety of Human Embryonic Stem Cell-Derived RPE Cells on a parylene membrane in patients with advanced, dry age-related macular degeneration.
- Macular Degeneration
- Age-Related Macular Degeneration
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
Frequently Asked Questions
Are there any available openings for participants in this clinical trial?
"Unfortunately, the information on clinicaltrials.gov appears to show that this particular trial is not actively seeking participants at this time; it was first posted in February of 2016 and last updated May 27th 2020. Nevertheless, there are currently 319 other studies available for enrollment."
In what geographic areas is this research endeavor taking place?
"Currently, this research initiative is accepting patients from 6 medical sites. These are located in Santa Barbara, Beverly Hills and Palm Desert among other areas. To minimize travelling demands associated with joining the trial, pick a study location that is closest to you."
Does this study allow for the enrolment of adults?
"The requirements for this medical trial are that patients must be between 55 and 85 years of age. For those under 18, there are 51 trials available; whereas 266 studies accept participants above the senior citizen threshold."
Could I meet the criteria for enrollment in this experiment?
"This clinical trial is admitting 16 participants, aged 55 to 85, who have dry macular degeneration. To be eligible for the study, these individuals must also meet many other criteria including: having physical evidence of at least 1.25 square millimeters of geographic atrophy in their eye; not being employees of any related medical sites; possessing enough good health so as to reasonably expect survival over five years post-treatment; having a best-corrected visual acuity (BCVA) score equal or worse than 20/200 and between 20/80 and 20/400 in the second half of patients respectively; medically suitable for surgical implant procedures"
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