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CS-121 APOC3 Base Editing in Severe Hypertriglyceridemia

15. juni 2026 opdateret af: CorrectSequence Therapeutics Co., Ltd

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

This is an open-label, single-arm, dose-escalation IIT clinical trial to evaluate the safety, tolerability, pharmacodynamics (PD), and pharmacokinetics (PK) of CS-121, an in vivo base editing therapy delivered by lipid nanoparticles targeting APOC3, in adult participants (18-65 years) with Severe Hypertriglyceridemia(sHTG).

Studieoversigt

Status

Ikke rekrutterer endnu

Intervention / Behandling

Detaljeret beskrivelse

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).

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

15

Fase

  • Tidlig fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

    • Anhui
      • Hefei, Anhui, Kina
        • The First Affiliated Hospital of Anhui Medical University
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Single Low Dose CS-121
Participants in this arm will receive a single low dose (0.5mg/kg) of CS-121.
CS-121 er en in vivo base-editeringsterapi formuleret i lipide nanopartikler til målrettet editering af APOC3-genet i hepatocytter.
Eksperimentel: Single Middle Dose CS-121
Participants in this arm will receive a single middle dose (0.7mg/kg) of CS-121.
CS-121 er en in vivo base-editeringsterapi formuleret i lipide nanopartikler til målrettet editering af APOC3-genet i hepatocytter.
Eksperimentel: Single High Dose CS-121
Participants in this arm will receive a single high dose (1.0mg/kg) of CS-121
CS-121 er en in vivo base-editeringsterapi formuleret i lipide nanopartikler til målrettet editering af APOC3-genet i hepatocytter.
Eksperimentel: Single selected Lower Dose 1 of CS-121
Participants in this arm will receive a single selected lower dose 1 of CS-121.
CS-121 er en in vivo base-editeringsterapi formuleret i lipide nanopartikler til målrettet editering af APOC3-genet i hepatocytter.
Eksperimentel: Single selected Lower Dose 2 of CS-121
Participants in this arm will receive a single selected lower dose 2 of CS-121
CS-121 er en in vivo base-editeringsterapi formuleret i lipide nanopartikler til målrettet editering af APOC3-genet i hepatocytter.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Treatment-Emergent Adverse Events (TEAEs)
Tidsramme: From screening to 12 months post last dosing
From screening to 12 months post last dosing
Dose-Limiting Toxicities (DLTs)
Tidsramme: Within 14 days after CS-121 infusion
Within 14 days after CS-121 infusion

Sekundære resultatmål

Resultatmål
Tidsramme
Koncentrationer af de aktive komponenter i CS-121 (sgRNA og mRNA)
Tidsramme: Fra baseline til 1 måned efter sidste dosering
Fra baseline til 1 måned efter sidste dosering
Change from Baseline in Fasting Serum Triglycerides (TG)
Tidsramme: Baseline through approximately 12 months post dosing
Baseline through approximately 12 months post dosing
Change from Baseline in Serum ApoC3 Protein Levels
Tidsramme: From baseline to 12 months post last dosing
From baseline to 12 months post last dosing

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

15. juni 2026

Primær færdiggørelse (Anslået)

15. marts 2028

Studieafslutning (Anslået)

31. juli 2028

Datoer for studieregistrering

Først indsendt

15. juni 2026

Først indsendt, der opfyldte QC-kriterier

15. juni 2026

Først opslået (Faktiske)

18. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

18. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

15. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

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Kliniske forsøg med Alvorlig hypertriglyceridæmi (sHTG)

Kliniske forsøg med CS-121

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