A Clinical Study for the Safety and Efficacy of Intravenous Infusion of NGGT006 in Treatment of Refractory Hypercholesterolemia
Overview
- Phase
- Early Phase 1
- Intervention
- NGGT006
- Conditions
- Refractory Hypercholesterolemia
- Sponsor
- Suzhou Municipal Hospital
- Enrollment
- 9
- Primary Endpoint
- Absolute change and percent change in LDL-C
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
This is an early phase 1, open-label, single-center, dose-escalation pilot trial to evaluate the safety and efficacy of an intravenous infusion of NGGT006 in patients with refractory Hypercholesterolemia diagnosed by gene testing for familial hypercholesterolemia. NGGT006 uses adeno-associated virus (AAV) as a vector, carrying a liver specific promoter and codon optimized human LDLR gene, driving the expression of LDLR protein with normal function and promoting the clearance of low-density lipoprotein cholesterol (LDL-C).
Detailed Description
Familial Hypercholesterolemia caused by common genetic mutations can be divided into heterozygous hypercholesterolemia (HeFH, Heterozygous Familial Hypercholesterolemia) and homozygous hypercholesterolemia (HoFH, Homozygous Familial Hypercholesterolemia). Refractory hypercholesterolemia was defined as an LDL-C level of 70 mg/dL or greater, or 100 mg/dL or greater, for patients with or without clinical ASCVD, respectively. A large proportion of patients with familial hypercholesterolemia belong to refractory hypercholesterolemia. This is an early phase 1, open-label, single-center, dose-escalation pilot trial to evaluate the safety and efficacy of a single intravenous infusion of NGGT006 in patients with refractory Hypercholesterolemia diagnosed by gene testing for familial hypercholesterolemia. 3-9 subjects will be enrolled and divided into 3 groups according to the principle of dose escalation, respectively administered intravenous infusion of NGGT006 at low dose (7.5e12vg/kg), medium dose (1.5e13vg/kg) and high dose (3e13vg/kg). All subjects will undergo 52 weeks of treatment observation and further 260 weeks of long-term follow-up.
Investigators
Yan Chen
President of Suzhou Municipal Hospital
Suzhou Municipal Hospital
Eligibility Criteria
Inclusion Criteria
- •18 ≤ age ≤ 55 years old;
- •A patient with a clear diagnosis of refractory hypercholesterolemia and confirmed by genetic testing to be familial hypercholesterolemia;
- •AAV binding antibody titer ≤1:80 and AAV neutralizing antibody ≤1:5;
- •18≤BMI (body mass index)≤35;
- •During the screening period, the subjects have received stable maximum tolerated dose of lipid-lowering drug treatment, but LDL-C was still ≥70mg/dL with clinical atherosclerotic cardiovascular disease; or LDL-C level was ≥ 100 mg/dL without clinical atherosclerotic cardiovascular disease: the highest tolerated dose refers to (the following must be met at the same time):
- •① Moderate to high doses of statins for ≥4 weeks, whether used alone or in combination with other lipid-lowering drugs; exceptions: subjects cannot tolerate statins; or subjects cannot receive statin treatment due to other reasons, such as low BMI, etc.;
- •② Ezetimibe ≥ 4 weeks;
- •③ Alirocumab 150mg Q2W or 300mg Q4W; evolocumab 140mg Q2W or 420mg Q4W; ≥8 weeks; And during the clinical trial process, any adjustment involving the type and dosage of lipid-lowering drugs must be approved by the researcher;
- •Stable healthy diet for ≥12 weeks, and can adhere to a healthy diet throughout the entire clinical trial;
- •Voluntarily sign the informed consent form and be willing to comply with the trial visit plan;
Exclusion Criteria
- •Secondary hyperlipidemia;
- •Use of other drugs or nutritional products that may affect blood lipids (such as fibrates) within 6 weeks;
- •Have received low-density lipoprotein apheresis (LDL apheresis) within the past 2 months;
- •Large weight fluctuations (≥5kg) in the past 2 months;
- •Positive for hepatitis B surface antigen, hepatitis C, human immunodeficiency virus (HIV)，syphilis test or other infections (such as Epstein-Barr virus, Mycoplasma pneumoniae, tuberculosis virus, HPV, Chlamydia pneumoniae, respiratory syncytial virus, Adenovirus and coxsackievirus group B, etc.);
- •Clinically significant abnormalities in liver function test: alanine aminotransferase (ALT) \>2 × upper limit of normal (ULN) and/or aspartate aminotransferase (AST) \>2 × ULN;
- •RR at the baseline \>160/100mmHg (one repeated measurement is allowed);
- •Uncontrollable myocardial infarction or heart failure, and those planning surgery within one year; or new acute coronary syndrome in the past six months;
- •Diabetes diagnosed within 3 months or with poor control (HbA1c \>9%);
- •Abnormal thyroid function, or those using thyroid hormone replacement therapy but poorly controlled (TSH within the normal range for \<12 weeks);
Arms & Interventions
NGGT006
3 doses of NGGT006 will be administered according to the principle of dose escalation
Intervention: NGGT006
Outcomes
Primary Outcomes
Absolute change and percent change in LDL-C
Time Frame: 52 weeks
Change in LDL-C concentration from baseline to week 52
Incidence of treatment-related adverse events (AE) and serious adverse events (SAE)
Time Frame: 52 weeks
Incidence of AE and SAE, as assessed by physical examinations, clinical laboratory parameters and adverse event reporting
Secondary Outcomes
- Absolute change and percent change in non-high density lipoprotein cholesterol(52 weeks)
- Absolute change and percent change in apolipoprotein B(52 weeks)
- Absolute change and percent change in total cholesterol(52 weeks)
- Absolute change and percent change in HDL-C(52 weeks)
- Absolute change and percent change in triglycerides(52 weeks)
- Absolute change and percent change in very low-density lipoprotein cholesterol(52 weeks)
- Absolute change and percent change in lipoprotein(a)(52 weeks)
- Absolute change and percent change in apolipoprotein A-I(52 weeks)