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NCT05991986Not yet recruiting

Preparation of Patient Autologous Induced Pluripotent Stem Cell-derived Retinal Cells for AMD

Production of Patient Autologous Induced Pluripotent Stem Cell-derived Retinal Cells for Age-related Macular Degeneration

Source: ClinicalTrials.gov · Last updated 28 Jan 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This project intends to collect participant somatic cells to prepare autologous induced pluripotent stem cell-derived retinal cells for future cell therapy of age-related macular degeneration patient.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
10 (estimated)
First submitted
26 Jul 2023
Start date
1 Aug 2025
Primary completion date
31 Jul 2026
Lead sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
NCT number
NCT05991986

What you commit to

  • Study type: Observational
  • Planned participants: 10
  • From 1 Aug 2025 to the primary completion date, 31 Jul 2026
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Other intraocular surgery histories besides cataract surgery;
  • Use glucocorticoids, immunosuppressive drugs, or antipsychotic drugs in the previous 3 months;
  • Use antipsychotic drugs in the previous 3 months, such as antidepressants drugs, antimanic drugs, etc.
  • Be participating in other intervention clinical trials or receiving other study medications;

Other illness

  • Macular atrophy caused by other diseases in addition to AMD;
  • Malignant tumor and history of malignancy;
  • Combined with severe systemic diseases, such as heart failure, liver disease, COPD, etc.
  • Combined with severe infectious diseases, such as HIV, HBV, HCV, syphilis, etc.
  • HCV-RNA positive, HBV-DNA \>103 IU/ml, or TB, etc., during the infectious period;
  • Allergy to tacrolimus or other macrolides;
  • A history of addiction to alcoholism or prohibited drugs;
  • Some other situations which might increase the risks of the subjects or interfere with clinical trials, such as mental disorders, cognitive dysfunction, etc.

Lab values

  • Severe heart failure or the left ventricular ejection fraction \<35% in the previous 6 months;
  • Dialysis or eGFR \<20ml/min/1.73m2;
  • Urine protein/urine creatinine ratio ≥1g/g;
  • Creatinine or albumin/urine creatinine ratio ≥600mg/g;
  • Chronic liver disease with ALT three times over the upper limit of normal value;
  • Use anticoagulant, or the platelet function is still not restored to normal after stopping antiplatelet drugs for 10 days;
  • Abnormal blood coagulation function or other laboratory tests;

Other

  • Any immune deficiency;
  • Lens opacities (affecting the central vision), glaucoma, uveitis, retinal detachment, inherited retinal dystrophy, optic neuropathy, and other ocular histories;
  • Informed refusal;

Who the study is looking for

  • Aged 55-80 years;
  • Clinical diagnosis is consistent with the definition of advanced age-related macular degeneration;
  • The BCVA of the target eye will be lower than 20/200;
  • -8.00 D \< refraction \< +8.00 D, 21 mm \< anteroposterior axis≤ 28 mm;
  • Voluntary as test subjects, informed consent, regular follow-up on time;
  • Voluntary as test subjects to join the associated clinical research on autologous iPSC-derived retinal cell therapy for AMD (ethical approval and informed consent documents will be applied and signed separately);

Age in the registry: 55 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.