PDE6A Gene Therapy for Retinitis Pigmentosa

"PIGMENT - Subretinal PDE6A gene therapy for retinitis pigmentosa" is an open mono-center, phase I/IIa trial with fellow-eye comparison.

The study begins with a detailed preliminary examination (Screening), comprises a total of 13 visits and ends after one year. In between, after the gene therapy injection (injection of the vector under the retina with one of four doses), regular controls are carried out at the Center for Ophthalmology Tübingen. Monitoring will be contimued after the first year, once a year two, three, four and five years after the injection. The study will take place exclusively at the Center for Ophthalmology in Tübingen and involves nine patients.

All patients participating in this study receive treatment, i.e. there is no placebo or sham treatment group. A 30-day safety distance is maintained between each patient and each group. An independent committee will decide, after each injection of three patients, which dose the following three patients will receive.

Patients can benefit from the treatment by slowing or stopping the loss of the rods and allowing them to function to a certain extent. Therefore, a possible benefit for patients may be that the vision problems will be improved by gene therapy. Such improvements could improve the overall quality of life and well-being. However, as no experience with gene therapy for retinitis pigmentosa in humans has yet been gained, we cannot promise any improvement. Within the scope of this study, patients will be given particularly intensive care and psychological support will also be offered in order to do everything for the patient's well-being and health during the study.

Time Schedule: Start of trial Q3/2019 (FPFV), end of recruitment Q3/2020, end of trial Q4/2025 (LPLV), duration of trial per patient: one year with four years of follow-up. The final study report will be prepared after completion of the four year follow-up period (5 years after treatment).

Inclusion criteria

• clinical diagnosis of retinitis pigmentosa
• confirmed mutation in PDE6A gene
• ≥ 18 years of age
• visual acuity ≥ 20/400
• no infection with Human Immundeficiency Virus (HIV)
• negative pregnancy test in women with childbearing potential (a woman who is two years post-menopausal or surgically sterile is not considered to be of childbearing potential)
• Male patients must agree to use condoms during the first 6 months post treatment.
• Female patients of childbearing potential must agree to use an effective method of birth control during the first 6 months post treatment.
• ability to understand and willingness to consent to study protocol

Exclusion criteria

Ocular (study eye & fellow eye)

• additional interfering ocular conditions with impact on study results (e.g. ocular opacity and advanced cataract, uveitis, amblyopia)
• recent (6 months) ocular surgery, intravitreal or subretinal implantation of a medical device
• disease causing mutations in another known retinitis pigmentosa gene
• ocular infection with herpes simplex virus in medical history
• history of ocular malignancies
• disorders of the internal retina (e.g. retinal detachment in the patients history)
• glaucoma defined as damage of the optic nerve
• vascular retinal occlusion
• diabetic patients suffering from retinopathy and/or macula edema
• any other retinopathy due to other diseases e.g. (but not limited to) arterial hypertension, trauma or acquired inflammatory diseases (uveitis serology), contraindication to pharmacological mydriasis (e.g. history of angle block glaucoma)
• absence of visual function on the contralateral eye Systemic
• systemic conditions (e.g. coronary heart disease, autoimmune disorders) which may affect study participation or outcome measures
• History of poorly controlled Diabetes Mellitus type 1 or type 2
• systemic illness or medically relevant abnormal laboratory values in blood analysis including renal and hepatic functions at inclusion
• patients treated with oral corticoids within 14 days prior inclusion
• current or recent participation in other study/or administration of biologic agent within the last three months
• known sensitivity to any compound used in the study
• contraindications to systemic immunosuppression
• contraindications in view of the planned surgery (e.g. but not limited to anaemia Hb<10g/dl, coagulopathy with PT/PTT >1,5 fold upper limit, hypertension with values above 180 mmHg systolic and 110 mmHg diastolic) including intolerance and contraindications to general anaesthesia
• intolerance to contrast agents used for diagnostic methods like angiography with fluoresceine or indocyanine green (e.g. but not limited to hyperthyroidism, hepatic insufficiency)
• subject/partner of childbearing potential unwilling to use adequate contraception for four months
• nursing or pregnant women
• any other cause that, in the investigator's opinion, renders potential subjects not suitable for the study