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Safety and Efficacy of Subretinal Transplantation of Clinical Human Embryonic Stem Cell Derived Retinal Pigment Epitheliums in Treatment of Retinitis Pigmentosa

Primary Purpose

Retinitis Pigmentosa

Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
Retinal pigment epitheliums transplantation
Sponsored by
Qi Zhou
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Retinitis Pigmentosa

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age above 18 and under 80 years of age, both gender, in good health.
  • Clinical diagnosis of retinitis pigmentosa, the results of eye electrophysiological examination accord with retinitis pigmentosa.
  • The BCVA of target eye will not be better than 20/400.
  • The BCVA of contralateral eye is not worse than 20/400.
  • Diopter is smaller than 8.00 D, axial 28 mm or less.
  • Voluntary as test subjects, signed informed consent, regular follow-up will be effected according to the specified time.

Exclusion Criteria:

  • Subject with other additional retinal diseases, like diabetic or hypertensive retinopathy vascular diseases.
  • Target eye ever have had a eye surgery;
  • Subject with active serious diseases of the digestive system, liver kidney impairment (ALT/AST) > 1.5 or any known liver disease, creatine > 1.3 mg/dL) and/serious temic diseases, such as cardiovascular tem, respiratory tem, nervous tem, endocrine tem urogenital tem diseases, etc.), the history of malignancy;
  • Have been ready for pregnancy during test, are lactating women;
  • Ready to birth of men during the test;
  • Subject with any immunodeficiency;
  • Subject in the immunosuppressive therapy in the current;
  • Subject with the tacrolimus or other large ring lactone class drug allergies;
  • Participate in any clinical subjects in nearly six months;
  • Has a history of alcohol or illicit drug abuse;
  • Poor adherence to complete studies;
  • Researchers believe that there may be an increased risk subjects or interfere with the clinical trials of any situation (such as when a patient is prone to mental tension, depression, mental illness, cognitive dysfunction, etc.).

Sites / Locations

  • Beijing Tongren Hospitol,Capital Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

retinal pigment epitheliums transplantation

Arm Description

Transplant clinical-grade hESC derived retinal pigment epitheliums into subretinal of patients with retinitis pigmentosa.The dosage is 150000.

Outcomes

Primary Outcome Measures

Adverse events and serious adverse events occurred within 1 year after transplantation
The occurrence of adverse events (AE), severe adverse events (SAE), treatment-related adverse events (TEAE), and clinically significant vital signs during the study period.

Secondary Outcome Measures

Improvement of visual function
The changes of BCVA and EDTRS were observed one year after surgery.

Full Information

First Posted
December 27, 2018
Last Updated
March 25, 2020
Sponsor
Qi Zhou
Collaborators
Beijing Tongren Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03944239
Brief Title
Safety and Efficacy of Subretinal Transplantation of Clinical Human Embryonic Stem Cell Derived Retinal Pigment Epitheliums in Treatment of Retinitis Pigmentosa
Official Title
Safety and Efficacy of Subretinal Transplantation of Clinical Human Embryonic Stem Cell Derived Retinal Pigment Epitheliums in Treatment of Retinitis Pigmentosa
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 2020 (Anticipated)
Primary Completion Date
October 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Qi Zhou
Collaborators
Beijing Tongren Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This project intends to transplant a clinical level human embryonic stem cells derived retinal pigment epithelium into subretinal space to treat eetinitis pigmentosa(RP) diseases. Through the statistical analysis EDTRS, BCVA, OCT, ERG, Fluorescein angiography, Ophthalmic AB ultrasound changes between before and after the treatment to assess the efficacy and safety 0f RPE transplants to treat RP disease.
Detailed Description
This project intends to transplant a clinical level human embryonic stem cells derived retinal pigment epithelium into subretinal space to treat eetinitis pigmentosa(RP) diseases. Through the statistical analysis EDTRS, BCVA, OCT, ERG, Fluorescein angiography, Ophthalmic AB ultrasound changes between before and after the treatment to assess the efficacy and safety 0f RPE transplants to treat RP disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinitis Pigmentosa

7. Study Design

Primary Purpose
Other
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
retinal pigment epitheliums transplantation
Arm Type
Experimental
Arm Description
Transplant clinical-grade hESC derived retinal pigment epitheliums into subretinal of patients with retinitis pigmentosa.The dosage is 150000.
Intervention Type
Biological
Intervention Name(s)
Retinal pigment epitheliums transplantation
Intervention Description
Subretinal transplantation of clinical human embryonic stem cell derived retinal pigment epitheliums.
Primary Outcome Measure Information:
Title
Adverse events and serious adverse events occurred within 1 year after transplantation
Description
The occurrence of adverse events (AE), severe adverse events (SAE), treatment-related adverse events (TEAE), and clinically significant vital signs during the study period.
Time Frame
one year
Secondary Outcome Measure Information:
Title
Improvement of visual function
Description
The changes of BCVA and EDTRS were observed one year after surgery.
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age above 18 and under 80 years of age, both gender, in good health. Clinical diagnosis of retinitis pigmentosa, the results of eye electrophysiological examination accord with retinitis pigmentosa. The BCVA of target eye will not be better than 20/400. The BCVA of contralateral eye is not worse than 20/400. Diopter is smaller than 8.00 D, axial 28 mm or less. Voluntary as test subjects, signed informed consent, regular follow-up will be effected according to the specified time. Exclusion Criteria: Subject with other additional retinal diseases, like diabetic or hypertensive retinopathy vascular diseases. Target eye ever have had a eye surgery; Subject with active serious diseases of the digestive system, liver kidney impairment (ALT/AST) > 1.5 or any known liver disease, creatine > 1.3 mg/dL) and/serious temic diseases, such as cardiovascular tem, respiratory tem, nervous tem, endocrine tem urogenital tem diseases, etc.), the history of malignancy; Have been ready for pregnancy during test, are lactating women; Ready to birth of men during the test; Subject with any immunodeficiency; Subject in the immunosuppressive therapy in the current; Subject with the tacrolimus or other large ring lactone class drug allergies; Participate in any clinical subjects in nearly six months; Has a history of alcohol or illicit drug abuse; Poor adherence to complete studies; Researchers believe that there may be an increased risk subjects or interfere with the clinical trials of any situation (such as when a patient is prone to mental tension, depression, mental illness, cognitive dysfunction, etc.).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wang Liu, Doctor
Phone
+86-01064807858
Email
wangliu@ioz.ac.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Hao Jie, Doctor
Phone
+86-01062558737
Email
haojie@ioz.ac.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhou Qi, Doctor
Organizational Affiliation
Institute of zoology, Chinese Academy of Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Tongren Hospitol,Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wei wen bin, Doctor
Phone
+86-01058265736
Email
weiwenbintr@163.com
First Name & Middle Initial & Last Name & Degree
Shen chang, Doctor
Phone
+86-010-58269804
Email
shenc_0526@163.com

12. IPD Sharing Statement

Learn more about this trial

Safety and Efficacy of Subretinal Transplantation of Clinical Human Embryonic Stem Cell Derived Retinal Pigment Epitheliums in Treatment of Retinitis Pigmentosa

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