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ACT201 Injection in Healthy Participants and Participants With Chronic Hepatitis B (CHB)

14 agosto 2026 aggiornato da: Xiamen Amoytop Biotech Co., Ltd.

A Single-Center, Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Phase I Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, Preliminary Efficacy, Drug Concentration-QTc Relationship, and Immunogenicity Profiles of Single and Multiple Doses of ACT201 Injection in Healthy Participants and Participants With Chronic Hepatitis B

This is a single-center, randomized, double-blind, placebo-controlled Phase I clinical trial consisting of two parts. Part 1 includes single ascending dose (SAD) and multiple ascending dose (MAD) cohorts conducted in healthy participants. Part 2 is a multiple ascending dose (MAD) trial enrolling HBeAg-negative chronic hepatitis B (CHB) participants with suppressed HBV DNA under stable nucleos(t)ide analog (NA) therapy.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

72

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Cina
        • Reclutamento
        • Huashan Hospital, Fudan University
        • Contatto:
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria:

Part 1:

  • Participants fully understand the purpose, nature and methods of the trial as well as potential adverse events, voluntarily participate in this trial and provide written informed consent;
  • Aged between 18 and 55 years old (inclusive) at the time of informed consent, male or female;
  • Body mass index meets specified criteria;
  • Physical examination, vital signs, laboratory tests, electrocardiogram and imaging examinations at screening are normal or abnormalities are considered clinically insignificant;
  • Participants (including their partners) are willing to use effective contraceptive measures from screening through 6 months after the last administration of investigational product, with no plans for pregnancy, sperm donation or oocyte donation.

Part 2:

  • Participants fully understand the purpose, nature and methods of the trial as well as potential adverse events, voluntarily participate in this trial and provide written informed consent;
  • Aged between 18 and 65 years old (inclusive) at the time of informed consent, male or female;
  • Body mass index meets specified criteria;
  • HBsAg-positive or HBV DNA-positive for at least 6 months, or previous liver biopsy confirming chronic HBV infection;
  • Receiving stable nucleos(t)ide analogue (NA) therapy at screening, with no planned changes to NA regimen during the trial;
  • Serum ALT ≤ 2 × ULN at screening; HBeAg, HBV DNA and HBsAg levels meet protocol-specified criteria;
  • Participants (including their partners) are willing to use effective contraceptive measures from screening through 6 months after the last administration of investigational product, with no plans for pregnancy, sperm donation or oocyte donation.

Exclusion Criteria:

Part 1:

  • Known or suspected hypersensitivity to ACT201 or its excipients; or participants with allergic diathesis (multiple drug and food allergies judged clinically significant by the Investigator).
  • History of clinically significant diseases involving cardiovascular, hematologic and lymphatic, urinary, endocrine, immune, psychiatric, or nervous systems (e.g., epilepsy).
  • Vital signs or laboratory examinations at screening meet the exclusion cut-off values specified in the protocol.
  • Use of any prescription drugs, over-the-counter medications, vitamin products or herbal medicines within 2 weeks prior to the first dose (topical medications with local effects are excluded).
  • Positive HBsAg, hepatitis B core antibody, hepatitis C antibody, human immunodeficiency virus antibody, or Treponema pallidum antibody at screening.
  • QTcF interval (QT corrected by Fridericia's formula) > 450 ms at screening.
  • Daily cigarette consumption exceeding 5 cigarettes within 3 months before screening.
  • History of drug abuse or illicit drug use within 1 year before screening, or positive urine drug screen at screening.
  • History of alcohol abuse within 6 months before screening (14 alcohol units per week: 1 unit = 285 mL beer with ~3.5% alcohol, or 25 mL spirits with ~40% alcohol, or 100 mL wine with ~10% alcohol), or positive breath alcohol test at screening.
  • Vaccination administered within 1 month before screening, or planned vaccination during the trial period.
  • Blood loss or blood donation ≥ 400 mL within 3 months before screening (menstrual bleeding in female participants excluded), or planned blood donation during the trial period.
  • Female participants who are breastfeeding or have a positive serum pregnancy test at screening.
  • Participation in any clinical trial with an investigational medicinal product/investigational device within 3 months before screening or within 5 half-lives (whichever is longer).
  • Any other condition deemed unsuitable for trial participation by the Investigator.

Part 2:

  • Major trauma or major surgery within 3 months before screening; or planned surgery during the trial period that may impair trial compliance or safety assessment as assessed by the Investigator.
  • Uncontrolled and clinically significant abnormalities other than chronic HBV infection, such as acute cerebrovascular disease, severe or unstable cardiac disease, uncontrolled diabetes, uncontrolled hypertension, uncontrolled dyslipidemia, etc.
  • History of other clinically significant liver diseases.
  • History of liver cirrhosis or progressive liver fibrosis; or liver stiffness measurement (LSM) ≥ 8.5 kPa at screening.
  • Alpha-fetoprotein > 50 ng/mL, or imaging suggestive of possible malignant hepatic lesions.
  • Past or current manifestations of hepatic decompensation.
  • History of extrahepatic diseases potentially related to HBV immune status.
  • History of vasculitis; or signs/symptoms suggestive of underlying vasculitis; or past/current other diseases potentially associated with vasculitic disorders.
  • Active infection requiring systemic antiviral or antibacterial treatment at screening, excluding HBV infection.
  • History of malignant tumors within 5 years before screening, except for specific curable cancers resected surgically.
  • Prior solid organ or bone marrow transplantation.
  • Use of systemic immunosuppressants within 3 months before the first dose of investigational product [short-term (≤7 days) glucocorticoids for prophylaxis or treatment of non-autoimmune diseases excluded]; use of immunomodulators or cytotoxic agents within 6 months before the first dose of investigational product.
  • Receipt of any oligonucleotide or small interfering RNA (siRNA) therapy within 12 months before the first dose of investigational product.
  • Coexisting indication for anticoagulant therapy or anticipated requirement for anticoagulation during the trial.
  • Any of the following laboratory results at screening, or other clinically significant abnormalities rendering the participant unsuitable for trial participation:

Platelet count < 125 × 10^9/L Absolute neutrophil count < 1.5 × 10^9/L Hemoglobin < 100 g/L Total bilirubin > 1.25 × ULN Serum albumin < 35 g/L Estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m^2 (calculated using the CKD-EPI formula) Prothrombin time international normalized ratio (INR) > 1.25 Positive hepatitis C antibody, human immunodeficiency virus antibody, or Treponema pallidum antibody

  • QTcF interval (QT corrected by Fridericia's formula) > 450 ms at screening, or other clinically significant electrocardiogram abnormalities identified at screening.
  • Known or suspected hypersensitivity to ACT201 or its excipients; or participants with allergic diathesis (multiple drug and food allergies judged clinically significant by the Investigator).
  • Daily cigarette consumption exceeding 5 cigarettes within 3 months before screening.
  • History of drug abuse or illicit drug use within 1 year before screening, or positive urine drug screen at screening.
  • History of alcohol abuse within 6 months before screening, or positive breath alcohol test at screening.
  • Vaccination administered within 1 month before screening, or planned vaccination during the trial period.
  • Blood loss or blood donation ≥ 400 mL within 3 months before screening (menstrual bleeding in female participants excluded), or planned blood donation during the trial period.
  • Female participants who are breastfeeding or have a positive serum pregnancy test at screening.
  • Participation in any clinical trial with an investigational medicinal product/investigational device within 3 months before screening or within 5 half-lives (whichever is longer).
  • Any other condition deemed unsuitable for trial participation by the Investigator.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: ACT201 Injection group

Part 1 SAD (Single Ascending Dose): Single-dose subcutaneous injection per assigned dose group.

Part 1 MAD (Multiple Ascending Dose) and Part 2: Subcutaneous injection per assigned dose group; treatment duration shall follow the study protocol.

Comparatore placebo: ACT201 Injection Placebo

Part 1 SAD (Single Ascending Dose): Single-dose subcutaneous injection administered per assigned dose group.

Part 1 MAD (Multiple Ascending Dose) and Part 2: Subcutaneous injection administered per assigned dose group; the treatment duration shall comply with the study protocol.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Safety: number of participants with adverse event (AE), serious adverse events (SAE) and clinically significant examination results.
Lasso di tempo: throughout the full study period,an average of 4 months
Assessments include vital signs, physical examinations, laboratory tests, and 12-lead electrocardiograms (ECGs).
throughout the full study period,an average of 4 months

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Plasma drug concentrations in healthy participants and participants withCHB
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Area Under the Concentration-Time Curve from time zero to the last measurable concentration(AUC₀-ₜ)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Area Under the Concentration-Time Curve from time zero to infinity(AUC₀-∞)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Apparent Volume of Distribution(Vd/F)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
First-order Elimination Rate Constant(Kel)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Elimination Half-life(t₁/₂)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Mean Residence Time(MRT)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Apparent Clearance(CL/F)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Minimum Plasma Concentration at Steady State(Cₘᵢₙ,ₛₛ)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Maximum Plasma Concentration at Steady State(Cₘₐₓ,ₛₛ)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Average Plasma Concentration at Steady State(Cₐᵥ,ₛₛ)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Area Under the Concentration-Time Curve over one dosing interval at steady state(AUC₀-τ)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Degree of Fluctuation (DF)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Accumulation Factor (Rac)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Urinary Concentration
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Cumulative Amount Excreted in Urine
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Cumulative Percentage of Dose Excreted in Urine
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Renal Clearance(CL)
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
HBsAg and HBsAb levels and changes from baseline among participants with CHB
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
HBsAg seroclearance rate among participants with CHB
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
HBsAg seroconversion rate among participants with CHB
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Placebo-corrected baseline-adjusted ΔQTc (ΔΔQTc) among healthy participants
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Anti-drug antibody (ADA) positive rate among healthy participants and participants with CHB
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months
Antibody titers among healthy participants and participants with CHB
Lasso di tempo: throughout the full study period,an average of 4 months
throughout the full study period,an average of 4 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Investigatori

  • Investigatore principale: Jing Zhang, Ph.D., Huashan Hospital
  • Investigatore principale: Wenhong Zhang, Ph.D., Huashan Hospital

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

6 agosto 2026

Completamento primario (Stimato)

1 marzo 2027

Completamento dello studio (Stimato)

1 aprile 2027

Date di iscrizione allo studio

Primo inviato

20 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

29 luglio 2026

Primo Inserito (Effettivo)

3 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

17 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • ACT201-4-1-001

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .