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Safety and Tolerability of Sub-retinal Transplantation of hESC Derived RPE (MA09-hRPE) Cells in Patients with Advanced Dry Age Related Macular Degeneration

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT01344993

Astellas Study ID

The unique identification code given by the study sponsor.

7316-CL-0002

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

N/A

Follow Trial

Condition

Age-related Vision Loss

Phase

These clinical trials are usually the first time an experimental treatment is studied in a small group of people.

Phase 1

Age

55 years - N/A

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Jun 2011 - Aug 2015

Masking

None (Open Label)

Enrollment number

13

A Phase I/II, Open-Label, Multi-Center, Prospective Study to Determine the Safety and Tolerability of Sub-retinal Transplantation of Human Embryonic Stem Cell Derived Retinal Pigmented Epithelial (MA09-hRPE) Cells in Patients with Advanced Dry AMD

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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Locations

Mass Eye and Ear

Boston, United States

Jules Stein Eye Institute, UCLA School of Medicine

Los Angeles, United States, 90095

Wills Eye Institute-Mid Atlantic Retina

Philadelphia, United States, 19107

Bascom Palmer Eye Institute

Miami, United States

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