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Clinical study of transplanting human retinal pigment epithelial cells for treatment of macular degeneration

Clinical study of transplanting human retinal pigment epithelial cells for treatment of macular degeneration

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-17010536
Enrollment
Unknown
Registered
2017-02-01
Start date
2017-02-15
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Macular degeneration

Interventions

Sponsors

EyeCure Therapeutics, Inc.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 50~80 years; 2. Diagnosed as atrophic macular degeneration (>250 microns of geographic atrophy involving central fovea); 3. BCVA of study eye equal to or worse than 20/200, BCVA of control eye equal to or better than 20/200; 4. Good health condition: Normal vital signs, electrocardiogram, routine blood and urine tests; 5. Understand and be able to sign the informed consent. 5. To be able to understand and willing to sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Hemoglobin1.5; creatinine level>1.3mg/dL; 3. Presence of glaucomatous optic neuropathy in the study eye; 4. Progressive Cataract causing difficulty of retina examination; 5. Any eye surgery other than cataract surgery within previous 3 months; 6. History of retina detachment repair in the study eye; 7. Uveitis or other intraocular inflammatory disease in the study eye; 8. Any other sight-threatening ocular disease; 9. Participation in any clinical trial of a drug by ocular or systemic administration within the past 6 months; 10. History of malignancy (except excised basal cell or squamous cell of skin); 11. History of myocardial infarction; 12. History of diabetes mellitus; 13. History of Parkinson's disease or Alzheimer's disease; 14. Any current immunosuppressive therapy other than intermittent or low dose corticosteroids; 15. Any other medical condition that affects patient compliance, patient safety, or the outcome of this clinical study.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity;

Secondary

MeasureTime frame
Optical coherent tomography (OCT);mERG;fundus photography;

Countries

China

Contacts

Public ContactLv Zhi-gang

EyeCure Therapeutics, Inc.

Gordon.Lv@eye-cure.com+86 13915312531

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026