PORTRAY: Study to Evaluate Sub-retinal Transplantation of Retinal Pigmented Epithelial Cells in Patients With Dry AMD
Study Details
Study Description
Brief Summary
To evaluate the safety of 3 regimens of short-term, low-dose systemic IMT as rejection prophylaxis prior to and/or following transplant of MA09-hRPE cells.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
This study will be a Phase 2, double-masked, randomized, parallel group, sham surgery/placebo control, multi-center trial. Subjects will be randomized in a 3:1 ratio to either the treatment or control group respectively. Subjects randomized to the treatment group will receive transplantation with 200,000 MA09-hRPE (human embryonic stem cell derived retinal pigmented epithelial)cells in one eye. Subjects randomized to the control group will have a sham surgery without transplantation of MA09-hRPE cells. The study eye must meet all eligibility criteria. If both eyes meet all eligibility criteria, then the study eye will be the eye with the worst Best Corrected Visual Acuity (BCVA) score at screening. If both eyes have identical BCVA scores, then the study eye will be chosen by the Investigator and the subject. There will be 3 cohorts, each with a different regimen of low-dose IMT [tacrolimus and mycophenolate mofetil (MMF)]. Subjects will be randomized to treatment or control within cohorts, defined by severity of BCVA in the study eye at Screening. Enrollment in Cohort 1 and 2 will be concurrent. Enrollment into Cohort 3 will begin once Cohort 2 is fully enrolled.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Sham Comparator: Control group Sham surgery and placebo immunosuppressive therapy (IMT) |
Drug: Placebo tacrolimus and mycophenolate mofetil
placebo
Procedure: Sham Surgery
Sham surgery
|
| Active Comparator: Active Group Sub-retinal transplantation of MA09-hRPE cells and IMT |
Biological: Sub-retinal transplantation of MA09-hRPE cells
transplantation
Drug: tacrolimus and mycophenolate mofetil
Immunosuppressive Agents
|
Outcome Measures
Primary Outcome Measures
- Number of subjects with evidence of graft failure or rejection. [18 months]
Secondary Outcome Measures
- Change in area of geographic atrophy by Optical coherence tomography [18 months]
Change from baseline to Week 78
- Change in area of geographic atrophy by Autofluorescence [18 months]
Change from baseline to Week 78
- Change in average Best Corrected Visual Acuity (BCVA) [18 months]
Change from baseline to Week 78
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Geographic atrophy (GA) secondary to AMD with no evidence of prior to active choroidal neovascularization (CNV) in the study eye.
-
BCVA in the study eye must be between 4 and 58 Early Treatment of Diabetic Retinopathy Study (EDTRS) letters (20/800 to 20/80; 0.025-0.25)
-
Subjects must be willing to take IMT and willing to discontinue any medication that has a known strong interaction with tacrolimus or mycophenolate mofetil (MMF)
Exclusion Criteria:
-
Macular atrophy due to causes other than AMD
-
Other sight-threatening ocular disease
-
Current or prior history of optic neuropathy, retinal dystrophy, retinitis pigmentosa, chorioretinitis, vasoocclusive disease, retinal vascular disease or retinal degenerative disease OTHER than AMD
-
History of uveitis
-
History of allergic reaction to sulfa drugs
-
Solid organ or bone marrow transplant recipient
-
History of malignancy within the previous 5 years (except for BCC (basal cell carcinoma), SCC (squamous cell carcinoma) or in-situ cervical)
-
History of myocardial infarction with past 12 months
-
History of clinically significant cardiac dysrhythmia
-
History of diabetes mellitus, bowel disease, tuberculosis
-
Prior treatment for non-exudative AMD
-
Intraocular, refractive or cataract surgery in the last 12 weeks
-
Prior retinal surgery, vitrectomy, macular laser photocoagulation, external beam radiation therapy, transpupillary thermotherapy, glaucoma filtration surgery or corneal surgery (except cataract surgery)
-
Receipt of gene transfer of cell transplant therapy in a prior clinical trial
-
Participation in any other interventional clinical trial within the last 12 weeks
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Wills Eye Institute | Philadelphia | Pennsylvania | United States | 19107 |
Sponsors and Collaborators
- Astellas Institute for Regenerative Medicine
Investigators
- Study Director: Medical Director, Astellas Institute for Regenerative Medicine
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 7317-CL-0002
- MA09-hRPE AMD 02 PORTRAY