- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07741461
ACT201 Injection in Healthy Participants and Participants With Chronic Hepatitis B (CHB)
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
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 1
Kontakter og lokationer
Studiekontakt
- Navn: Jing Zhang, Ph.D.
- Telefonnummer: 021-52887926
- E-mail: Zhangj_fudan@163.com
Undersøgelse Kontakt Backup
- Navn: Wenhong Zhang, Ph.D.
- Telefonnummer: 18121186602
- E-mail: zhangwenhong@fudan.edu.cn
Studiesteder
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina
- Rekruttering
- Huashan Hospital, Fudan University
-
Kontakt:
- Jing Zhang, Ph.D.
- Telefonnummer: 021-52887926
- E-mail: Zhangj_fudan@163.com
-
Kontakt:
- Wenhong Zhang, Ph.D.
- Telefonnummer: 18121186602
- E-mail: zhangwenhong@fudan.edu.cn
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Sekventiel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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. |
|
Placebo komparator: 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. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Safety: number of participants with adverse event (AE), serious adverse events (SAE) and clinically significant examination results.
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Plasma drug concentrations in healthy participants and participants withCHB
Tidsramme: 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)
Tidsramme: 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-∞)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: throughout the full study period,an average of 4 months
|
throughout the full study period,an average of 4 months
|
|
Mean Residence Time(MRT)
Tidsramme: throughout the full study period,an average of 4 months
|
throughout the full study period,an average of 4 months
|
|
Apparent Clearance(CL/F)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: throughout the full study period,an average of 4 months
|
throughout the full study period,an average of 4 months
|
|
Degree of Fluctuation (DF)
Tidsramme: throughout the full study period,an average of 4 months
|
throughout the full study period,an average of 4 months
|
|
Accumulation Factor (Rac)
Tidsramme: throughout the full study period,an average of 4 months
|
throughout the full study period,an average of 4 months
|
|
Urinary Concentration
Tidsramme: 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
Tidsramme: 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
Tidsramme: throughout the full study period,an average of 4 months
|
throughout the full study period,an average of 4 months
|
|
Renal Clearance(CL)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: throughout the full study period,an average of 4 months
|
throughout the full study period,an average of 4 months
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Jing Zhang, Ph.D., Huashan Hospital
- Ledende efterforsker: Wenhong Zhang, Ph.D., Huashan Hospital
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- ACT201-4-1-001
Plan for individuelle deltagerdata (IPD)
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