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Clinical study to evaluate the safety and tolerability of SPVN06 (novel gene therapy) in a subset of patients with rod cone dystrophy (RCD).

Phase 1
Recruiting
Conditions
Inherited retinal dystrophies
MedDRA version: 20.0Level: PTClassification code: 10019899Term: Hereditary retinal dystrophy Class: 100000004850
Therapeutic area: Diseases [C] - Eye Diseases [C11]
Registration Number
CTIS2022-501250-12-01
Lead Sponsor
Sparingvision
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
33
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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