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Clinical Trial of Autologous Intravitreal Bone-marrow CD34+ Stem Cells for Retinopathy

University of California (UC) Davis logo

University of California (UC) Davis

Status and phase

Active, not recruiting
Phase 1

Conditions

Retina Vein Occlusion
Non-exudative Age-related Macular Degeneration
Retinitis Pigmentosa
Hereditary Macular Degeneration
Diabetic Retinopathy

Treatments

Drug: CD34+ bone marrow stem cells intravitreal

Study type

Interventional

Funder types

Other

Identifiers

NCT01736059
BMSCRetPilot (Other Identifier)
906595

Details and patient eligibility

About

This pilot study is to determine whether it would be safe and feasible to inject CD34+ stem cells from bone marrow into the eye as treatment for patients who are irreversibly blind from various retinal conditions.

Full description

In this pilot clinical trial, eyes with irreversible vision loss from retinal degenerative conditions (macular degeneration or retinitis pigmentosa) or retinal vascular disease (diabetic retinopathy or retinal vein occlusion) will be treated with intravitreal injection of autologous CD34+ stem cells isolated from bone marrow aspirate under Good Manufacturing Practice conditions. This study will determine whether there are any major safety and feasibility concerns using this therapy. Patients will be followed for 6 months after treatment by serial comprehensive eye examination supplemented with various retinal imaging and diagnostic tests.

Enrollment

15 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age >18 years of age
  • visual acuity 20/100 to CF
  • duration of vision loss > 3 months
  • vision loss from macular degeneration, retinitis pigmentosa, retinal vein occlusion or diabetic retinopathy
  • the study eye has the worse visual acuity
  • no active eye or systemic disease
  • no history of macular edema or retinal/choroidal neovascularization requiring treatment within 6 months
  • no significant media opacity
  • no coagulopathy or other hematologic abnormality
  • no concurrent immunosuppressive therapy
  • able to keep follow-up for 6 months

Exclusion criteria

  • allergy to fluorescein dye
  • other concurrent retinal or optic nerve disease affecting vision

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Stem cell treated
Experimental group
Treatment:
Drug: CD34+ bone marrow stem cells intravitreal

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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