RecruitingPhase 1NCT06237777
A Clinical Study Evaluating the Safety, Tolerability and Initial Efficacy of SKG0106 Intravitreal Injection in Diabetic Macular Edema (DME) Patients
An Open, Dose-escalation Clinical Study Evaluating the Safety, Tolerability and Initial Efficacy of SKG0106 Intravitreal Injection in Diabetic Macular Edema (DME) Patients in China
Sponsor
Wang Min
Enrollment
18 participants
Start Date
May 1, 2024
Study Type
INTERVENTIONAL
Conditions
Summary
This is a clinical study to evaluate the safety, tolerability and initial efficacy of SKG0106 intravitreal injection in diabetic macular edema (DME) patients.
Eligibility
Min Age: 18 Years
Inclusion Criteria6
- Written informed consent must be obtained prior to all assessments.
- Age ≥18 years at screening.
- Type 1 or type 2 diabetes mellitus at screening.
- Study eye criteria:
- Decreased visual acuity attributable primarily to DME.
- DME involves the macular center.
Exclusion Criteria10
- Active proliferative diabetic retinopathy in the study eye.
- Any current or previous ocular disease in the study eye other than DME that could interfere with macular evaluation or affect central vision at screening or baseline.
- Any active intraocular or periocular infection or active intraocular inflammation of the study eye at screening or baseline.
- History of idiopathic or autoimmune uveitis in the study eye at screening or baseline.
- Prior gene therapy in either eye.
- History of vitreoretinal surgery in the study eye.
- Uncontrolled blood pressure at screening or baseline defined as systolic blood pressure (SBP) ≥160 mmHg or diastolic blood pressure (DBP) ≥100 mmHg.
- History of treated or untreated malignancy of any organ system within the past 5 years.
- Pregnant or lactating women.
- Women of reproductive age, defined as all women who are biologically capable of being pregnant, unless they use highly effective contraceptive methods between the time of study drug administration and 3 months after EOS (end of study).
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Interventions
GENETICSKG0106 intravitreal injection dose level 1, 2 or 3
SKG0106 is a recombinant adeno-associated virus (rAAV) vector-based in vivo gene therapeutic product.
Locations(2)
View Full Details on ClinicalTrials.gov
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NCT06237777
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