- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07657780
CS-121 APOC3 Base Editing in Severe Hypertriglyceridemia
A Clinical Study to the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of CS-121, an In Vivo Base Editing Therapy Delivered by Lipid Nanoparticles Targeting APOC3 for the Treatment of Severe Hypertriglyceridemia in Adults
연구 개요
상세 설명
CS-121 is an investigational, in vivo base editing therapy delivered by lipid nanoparticles (LNPs) targeting the APOC3 gene in the liver. By introducing precise base edits at specific APOC3 loci, CS-121 is intended to mimic naturally occurring protective mutations that reduce ApoC3 expression, thereby restoring triglyceride clearance pathways and lowering pancreatitis risk. Preclinical studies in transgenic mouse and non-human primate models demonstrated dose-dependent APOC3 editing, reductions in serum ApoC3 protein and triglyceride levels, and acceptable safety profiles, supporting advancement into human evaluation.
This open-label, single-arm, dose-escalation early exploratory trial designed to evaluate the safety, tolerability, PK/PD characteristics and preliminary efficacy of CS-121 in patients with sHTG. Based on the properties of gene editing therapy, the primary focus of the study is to identify the optimal biological dose (OBD) rather than the traditional maximum tolerated dose (MTD).
연구 유형
등록 (추정된)
단계
- 초기 1단계
연락처 및 위치
연구 연락처
- 이름: Xiaokai Li
- 전화번호: +8618686610731
- 이메일: xiaokai.li@correctsequence.com
연구 장소
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Anhui
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Hefei, Anhui, 중국
- The First Affiliated Hospital of Anhui Medical University
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연락하다:
- Huan Zhou
- 전화번호: +8613665527160
- 이메일: zhouhuanbest@vip.163.com
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Male or female participants aged 18 years ≤ age < 65 years.
- The serum triglyceride levels of the participants failed to be effectively controlled under the standard treatment regimen (or the medication that is available and tolerable as recommended by clinical practice) and were defined as having at least 3 records of different fasting triglyceride levels ≥ 5.65 mmol/L (500 mg/dL) within 2 years..
- The screening period should include at least two different days with a TG level of ≥ 5.65 mmol/L (500 mg/dL), with an interval of at least 7 days.
- Able to sign informed consent and comply with the requirements and restrictions specified in the informed consent form and the protocol.
- Female participants must meet one of the following: be not of childbearing potential (e.g., documented hysterectomy, bilateral salpingectomy/sterilization, or ≥1 year postmenopausal); or, if of childbearing potential, have a negative pregnancy test at screening and be willing to use strict and effective contraception (e.g., abstinence, pharmacologic, or barrier methods) during the study. Male participants with reproductive potential must agree to use strict and effective contraception (e.g., abstinence, pharmacologic, or barrier methods) throughout the entire post-dose observation period; males without reproductive potential must provide supporting medical history (e.g., post-vasectomy).
Exclusion Criteria:
- Currently participating in other interventional clinical studies, or having an insufficient washout period of less than 5 half-lives or 30 days (whichever is longer) since the last administration of other investigational drugs.
- Used antisense oligonucleotide (ASO)-based or small interfering RNA (siRNA)-based lipid-lowering drugs targeting APOC3 within 3 months prior to study drug administration.
- Requires long-term use of systemic corticosteroids and steroid drugs and cannot discontinue the medication.
- Patients who experienced acute pancreatitis within 4 weeks prior dosing.
- History of acute coronary syndrome (ACS) within 6 months before dosing, such as myocardial infarction or unstable angina, or prior coronary revascularization (such as coronary artery bypass grafting), angioplasty or stent implantation.
- In the investigator's judgment to be unsuitable for the study drug due to receipt of major surgery within 3 months before dosing.
- Any of the following laboratory abnormalities at screening:.
- ALT or AST ≥2 × ULN;
- Total bilirubin ≥2 × ULN;
- eGFR <30 mL/min/1.73 m²
- HbA1c ≥9%;
- Absolute neutrophil count < 1.0 × 109/L
- Hemoglobin (female)< 100 g/L, Hemoglobin (male) < 110 g/L
- Platelet count < 100 × 109/L
- Coagulation function abnormalities judged by the investigator as unsuitable for CS-121 administration.
- Positive results for HBsAg, dual positivity for HCV antibody and RNA, positive for HIV, or positive for Treponema pallidum infection.
- Known major organ diseases, mental disorders, Cushing's syndrome, hypothyroidism, history of lymphoproliferative disorders, or malignant tumors in any organ system, which are judged by the investigator as unsuitable for study participation due to potential intolerance to adverse events such as cytokine-Release-Storm.
- Concomitant medications/treatments judged by the investigator to affect lipid metabolism, liver and kidney function, coagulation function, or interfere with the efficacy evaluation of the study drug.
- Patients of childbearing potential who are planning pregnancy, breastfeeding, or have fertility plans.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 순차적 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: Single Low Dose CS-121
Participants in this arm will receive a single low dose (0.5mg/kg) of CS-121.
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CS-121은 간세포에서 APOC3 유전자를 표적으로 하는 지질 나노입자로 제형화된 생체 내(in vivo) 베이스 편집 치료제입니다.
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실험적: Single Middle Dose CS-121
Participants in this arm will receive a single middle dose (0.7mg/kg) of CS-121.
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CS-121은 간세포에서 APOC3 유전자를 표적으로 하는 지질 나노입자로 제형화된 생체 내(in vivo) 베이스 편집 치료제입니다.
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실험적: Single High Dose CS-121
Participants in this arm will receive a single high dose (1.0mg/kg) of CS-121
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CS-121은 간세포에서 APOC3 유전자를 표적으로 하는 지질 나노입자로 제형화된 생체 내(in vivo) 베이스 편집 치료제입니다.
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실험적: Single selected Lower Dose 1 of CS-121
Participants in this arm will receive a single selected lower dose 1 of CS-121.
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CS-121은 간세포에서 APOC3 유전자를 표적으로 하는 지질 나노입자로 제형화된 생체 내(in vivo) 베이스 편집 치료제입니다.
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실험적: Single selected Lower Dose 2 of CS-121
Participants in this arm will receive a single selected lower dose 2 of CS-121
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CS-121은 간세포에서 APOC3 유전자를 표적으로 하는 지질 나노입자로 제형화된 생체 내(in vivo) 베이스 편집 치료제입니다.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Treatment-Emergent Adverse Events (TEAEs)
기간: From screening to 12 months post last dosing
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From screening to 12 months post last dosing
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Dose-Limiting Toxicities (DLTs)
기간: Within 14 days after CS-121 infusion
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Within 14 days after CS-121 infusion
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2차 결과 측정
결과 측정 |
기간 |
|---|---|
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CS-121의 활성 성분(sgRNA 및 mRNA)의 농도
기간: 기저선에서 마지막 투약 후 1개월까지
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기저선에서 마지막 투약 후 1개월까지
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Change from Baseline in Fasting Serum Triglycerides (TG)
기간: Baseline through approximately 12 months post dosing
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Baseline through approximately 12 months post dosing
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Change from Baseline in Serum ApoC3 Protein Levels
기간: From baseline to 12 months post last dosing
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From baseline to 12 months post last dosing
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- CS-121-06
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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