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
調査の概要
詳細な説明
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).
研究の種類
入学 (推定)
段階
- 初期フェーズ 1
連絡先と場所
研究連絡先
- 名前:Xiaokai Li
- 電話番号:+8618686610731
- メール:xiaokai.li@correctsequence.com
研究場所
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Anhui
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Hefei、Anhui、中国
- The First Affiliated Hospital of Anhui Medical University
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コンタクト:
- Huan Zhou
- 電話番号:+8613665527160
- メール:zhouhuanbest@vip.163.com
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:非ランダム化
- 介入モデル:順次割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的: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-121は、肝細胞におけるAPOC3遺伝子の標的編集のために脂質ナノ粒子に製剤化されたin vivo塩基編集療法です。
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実験的: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-121は、肝細胞におけるAPOC3遺伝子の標的編集のために脂質ナノ粒子に製剤化されたin vivo塩基編集療法です。
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実験的: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-121は、肝細胞におけるAPOC3遺伝子の標的編集のために脂質ナノ粒子に製剤化されたin vivo塩基編集療法です。
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実験的: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-121は、肝細胞におけるAPOC3遺伝子の標的編集のために脂質ナノ粒子に製剤化されたin vivo塩基編集療法です。
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実験的: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-121は、肝細胞におけるAPOC3遺伝子の標的編集のために脂質ナノ粒子に製剤化されたin vivo塩基編集療法です。
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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Treatment-Emergent Adverse Events (TEAEs)
時間枠: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)
時間枠:Within 14 days after CS-121 infusion
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Within 14 days after CS-121 infusion
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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CS-121の有効成分(sgRNAおよびmRNA)の濃度
時間枠:最終投与後1ヵ月までのベースラインから
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最終投与後1ヵ月までのベースラインから
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Change from Baseline in Fasting Serum Triglycerides (TG)
時間枠: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
時間枠:From baseline to 12 months post last dosing
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From baseline to 12 months post last dosing
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協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- CS-121-06
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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