Study Details

Long Term Follow Up of Sub-retinal Transplantation of hESC Derived RPE Cells in Patients with AMD

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.
NCT02463344

Astellas Study ID

The unique identification code given by the study sponsor.

7316-CL-0005

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

Condition

Age-related Vision Loss

Phase

N/A

Age

55 years - N/A

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are identified as belonging to study groups and are assessed for biomedical or health outcomes. Participants may receive diagnostic, therapeutic, or other types of interventions, but the investigator does not assign participants to a specific interventions/treatment.

Observational

Trial Dates

Feb 2013 - Aug 2019

Masking

Not Available

Enrollment number

11

Long term follow up to 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

Bascom Palmer Eye Institute

Miami, United States, 33136

Wills Eye Institute-Mid Atlantic Retina

Philadelphia, United States, 19107

Mass Eye and Ear

Boston, United States, 02114-3002

Jules Stein Eye Institute, UCLA School of Medicine

Los Angeles, United States, 90095