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CS-121 APOC3 Base Editing in Severe Hypertriglyceridemia

15. juni 2026 oppdatert av: 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).

Studieoversikt

Status

Har ikke rekruttert ennå

Intervensjon / Behandling

Detaljert 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).

Studietype

Intervensjonell

Registrering (Antatt)

15

Fase

  • Tidlig fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Anhui
      • Hefei, Anhui, Kina
        • The First Affiliated Hospital of Anhui Medical University
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Sekvensiell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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-redigeringsbehandling formulert i lipidnanopartikler for målrettet redigering av APOC3-genet i hepatocytter.
Eksperimentell: 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-redigeringsbehandling formulert i lipidnanopartikler for målrettet redigering av APOC3-genet i hepatocytter.
Eksperimentell: 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-redigeringsbehandling formulert i lipidnanopartikler for målrettet redigering av APOC3-genet i hepatocytter.
Eksperimentell: 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-redigeringsbehandling formulert i lipidnanopartikler for målrettet redigering av APOC3-genet i hepatocytter.
Eksperimentell: 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-redigeringsbehandling formulert i lipidnanopartikler for målrettet redigering av APOC3-genet i hepatocytter.

Hva måler studien?

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
Konsentrasjoner av de aktive komponentene i CS-121 (sgRNA og mRNA)
Tidsramme: Fra baseline til 1 måned etter siste dosering
Fra baseline til 1 måned etter siste 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

15. juni 2026

Primær fullføring (Antatt)

15. mars 2028

Studiet fullført (Antatt)

31. juli 2028

Datoer for studieregistrering

Først innsendt

15. juni 2026

Først innsendt som oppfylte QC-kriteriene

15. juni 2026

Først lagt ut (Faktiske)

18. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

18. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

15. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

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UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

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Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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