rAAV.hCNGA3: Single subretinal injection of rAAV.hCNGA3
Study summary
The purpose of this study is to proof the safety and efficacy of a single bilateral subretinal injection of rAAV.hCNGA3 in adult and minor patients with CNGA3-linked achromatopsia.
Eligibility
Sex
ALL
Min age
6 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria (Both Eyes)
* clinical diagnosis of achromatopsia
* 6-12 years of age
* ≥ 18 years of age
* confirmed mutation in CNGA3
* BCVA ≥ 20/400
* a minimal outer nuclear layer thickness of 10µm at 3° eccentricity (normal = 38±6µm)
* ability to understand and willingness to consent to study protocol
* no infection with Human Immundeficiency Virus (HIV)
* 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.
* 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)
Exclusion Criteria
* any other retinopathy due to other diseases e.g. (but not limited to) arterial hypertension, trauma or acquired inflammatory diseases (uveitis serology) , retinopathy of the premature
* systemic conditions (e.g. coronary heart disease, congenital/genetic conditions, autoimmune disorders) which may affect study participation or outcome measures
* current or recent participation in other study or administration of biologic agent within the last three months
* recent (6 months) ocular surgery, intravitreal or subretinal implantation of a medical device
* known sensitivity to any compound used in the study
* contraindications to systemic immunosuppression
* subject/partner of childbearing potential unwilling to use adequate contraception for six months after dosing
* nursing or pregnant female subject women
* any other cause that, in the investigator's opinion, renders potential subjects not suitable for the study
* mutations in another achromatopsia gene
* contraindications in view of the planned surgery (e.g. anaemia Hb\<8g/dl, severe coagulopathy, severe blood pressure fluctuations) including intolerance and contraindications to general anaesthesia
* ocular opacity and mature cataract
* 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
* history of poorly controlled (HbA1c \> 7%) Diabetes Mellitus type 1 or type 2
* patients treated with systemic corticoids within 14 days prior inclusion
* systemic illness or medically significant abnormal laboratory values \>3 UNL in blood analysis including renal and hepatic functions at inclusion
* absence of vision on the other contralateral eye
* contraindication to pharmacological mydriasis (e.g. history of angle block glaucoma)
Primary outcome measure(s)
Safety (AE). Number of Participants With Abnormal Laboratory Values and/or Adverse Events That Are Related to Treatment — Day 0 - Day 365 Safety as the primary endpoint will be assessed by clinical examination of ocular inflammation (slit lamp, fundus biomicroscopy, fundus photography. Systemic safety will be assessed by vital signs, routine clinical chemistry testing (including CRP, ESR) and full/differential blood counts. Immunopathology essays will include specific enzyme-linked immunosorbent assays for humoral antibodies against rAAV8 capsid protein. Biodistribution will be monitored by polymerase chain reaction studies on rAAV8 genome in blood, urine, saliva and tear fluid.
Trial sites (1)
Facility
City
Region
Status
University Hospital Tuebingen, Center for Ophthalmology
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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