- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07614308
A Phase Ⅰ b Clinical Study of ART101 Injection
A Phase Ib Clinical Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of a Single Subcutaneous Injection of ART101 Injection in Patients With Hypertension
This is an open-label, single dose Phase Ib clinical study designed to evaluate the safety, tolerability, efficacy, pharmacokinetics (PK), and pharmacodynamics (PD) of a single subcutaneous injection of ART101 in patients with hypertension.
The study plans to include 2 dose groups: ART101 600 mg and 800 mg. It is planned to enroll 8 subjects per group, for a total of 16 subjects.
For dose escalation, a Safety Review Committee (SRC) will be established. If a dose group meets the dose escalation termination criteria, or if significant safety events occur during the dose escalation observation period (within 30 days), the SRC will discuss with the sponsor to decide whether to continue the dose escalation.
The screening period for this study is ≤6 weeks. After fasting for at least 8 hours, subjects will receive a single subcutaneous injection of ART101 on Day 1 (D1). The treatment observation period is 24 weeks. At the end of the 24-week treatment observation period, if the subject's angiotensinogen level has not recovered to more than 50% of the baseline level, the follow-up period will be extended. Subjects will continue to receive visits every 12 weeks until the angiotensinogen level recovers to more than 50% of the baseline level, or until 48 weeks after administration of the investigational drug, whichever occurs first.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
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Jiangsu
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Suzhou, Jiangsu, Kina
- Suzhou Arnatar Therapeutics Co., Ltd
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Aged 18 to 65 years (inclusive) at the time of signing the informed consent form (ICF), male or female.
- Patients diagnosed with essential hypertension.
Previously untreated for hypertension, or previously treated with ≤2 types of antihypertensive medications and have undergone at least a 2-week washout period prior to Visit 2 (for long-acting antihypertensive drugs, a 4-week washout period is required, e.g., chlorthalidone, amlodipine, etc.), and meet the following blood pressure measurement criteria:
① During the screening period and at baseline, seated systolic blood pressure (SBP) measured by OBPM is ≥140 mmHg and <160 mmHg;
② During the screening period, without the use of antihypertensive medications, 24-hour ABPM shows mean SBP ≥130 mmHg and <160 mmHg.
- Male subjects with body weight ≥50.0 kg, female subjects with body weight ≥45.0 kg, and Body Mass Index (BMI) between 18.0 and 35.0 kg/m² (inclusive).
- Maintained a normal diet and salt intake for at least 4 weeks prior to the administration of the investigational product, and has no plans to significantly change diet or body weight during the study.
- Subjects of childbearing potential, or male subjects with partners of childbearing potential, must agree to use effective contraception from the signing of the ICF until 24 weeks after the administration of the investigational product, and must refrain from donating sperm or eggs.
Voluntarily signed a written informed consent form, understands the study procedures and content, is able to communicate effectively with the investigator, and is willing to comply with study-related regulations.
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Exclusion Criteria:
1. Secondary hypertension, including but not limited to renovascular hypertension (unilateral or bilateral renal artery stenosis), coarctation of the aorta, primary aldosteronism, Cushing's syndrome, pheochromocytoma, polycystic kidney disease, or drug-induced hypertension.
2. During the screening period and at baseline, seated diastolic blood pressure (DBP) measured by OBPM is ≥120 mmHg or <75 mmHg.
3. History or current presence of hypotension, orthostatic hypotension, or postural orthostatic tachycardia syndrome (POTS).
4. Occurrence of cardiovascular or cerebrovascular events within 6 months prior to screening, including but not limited to stroke, transient ischemic attack (TIA), myocardial infarction, unstable angina, coronary artery bypass graft (CABG) surgery, percutaneous coronary intervention (PCI), or hospitalization due to heart failure.
5. Presence of congestive heart failure (New York Heart Association [NYHA] functional class III-IV), or clinically significant valvular heart disease or arrhythmia (e.g., persistent atrial fibrillation) as determined by the investigator.
6. Diagnosis of congenital long QT syndrome, family history of congenital long QT syndrome, or presence of an implanted pacemaker or automatic implantable cardioverter-defibrillator (AICD).
7. Presence of clinically significant electrocardiogram (ECG) abnormalities as judged by the investigator at screening.
8. Comorbid type 1 diabetes at screening, or poorly controlled type 2 diabetes (Glycated Hemoglobin [HbA1c] >9.0%).
9. Comorbid chronic liver disease, including but not limited to liver fibrosis and cirrhosis.
10. Diagnosis of malignancy, or a history of malignancy within 5 years prior to signing the ICF (except for cured non-melanoma skin cancer and cervical intraepithelial neoplasia with no signs of recurrence).
11. Accompanied by other severe, progressive, or uncontrolled diseases, including but not limited to diseases of the endocrine, hematological, urinary, hepatobiliary, respiratory, neurological, cardiovascular, gastrointestinal systems, or infectious diseases, wherein the investigator assesses that participation in the study would increase the risk to the subject.
12. Positive for Hepatitis B surface antigen (HBsAg), Hepatitis C antibody (HCV-Ab), Treponema pallidum antibody (TP-Ab), or Human Immunodeficiency Virus antibody (HIV-Ab) at screening.
13. Laboratory abnormalities during the screening period as follows:
- Platelet count <100×10⁹/L;
- Hemoglobin <90 g/L;
- eGFR <60 mL/min/1.73 m² (calculated by CKD-EPI 2021 equation);
- Alanine aminotransferase (ALT) or Aspartate aminotransferase (AST) >1.5×ULN;
- Total Bilirubin (TBIL) >2×ULN (for subjects with Gilbert's syndrome, TBIL >3×ULN);
Serum potassium >1.0×ULN. 14. Known allergy to oligonucleotides, drugs containing N-acetylgalactosamine (GalNAc), the investigational product used in this trial and its components, or drugs of the same class.
15. Presence of tattoos, scars, or birthmarks on the abdomen, upper arm, or thigh that may affect the assessment of injection site reactions.
16. Undergone major surgery within 3 months prior to the administration of the investigational product, or planning to undergo elective surgery during the study period.
17. Donated blood or experienced significant blood loss (≥400 mL) within 3 months prior to the administration of the investigational product (excluding menstrual bleeding in females), or received a blood transfusion within 12 months prior to the administration of the investigational product.
18. Received a live vaccine within 4 weeks prior to the administration of the investigational product, or planning to receive a live vaccine during the study period.
19. Use of any antisense oligonucleotide (ASO) or small interfering RNA (siRNA) drugs within 12 months prior to the administration of the investigational product.
20. History of drug or substance abuse, or positive urine drug abuse screening during the screening period.
21. Smoking history of ≥5 cigarettes per day within 3 months prior to screening, or plan to smoke ≥5 cigarettes per day during the study period after signing the ICF.
22. Alcohol intake of ≥14 units/week within 4 weeks prior to screening (1 unit = 10 g of alcohol, ≈360 mL of beer / 150 mL of wine / 45 mL of 40% spirits), or unwillingness to comply with alcohol restriction requirements during the study period after signing the ICF (alcohol consumption <14 units/week, abstinence from alcohol for 24 hours prior to each visit), or positive alcohol breath test during screening.
23. Consumed caffeine-containing beverages (e.g., coffee, tea, caffeinated soda, and cola) within 2 days prior to the administration of the investigational product, or unwillingness to comply with requirements regarding caffeine beverage intake during the study period after signing the ICF (<5 cups of coffee/day).
24. Participation in other clinical trials within 3 months prior to the administration of the investigational product, or currently participating in other clinical trials (subjects may be enrolled in this study if they withdrew from the previous study before treatment, i.e., were not randomized or did not receive treatment).
25. Pregnant or lactating women. 26. Individuals whose job nature requires night shifts, early shifts, or rotating shifts, which may lead to blood pressure fluctuations or affect circadian blood pressure rhythms.
27. Use or planned use of other antihypertensive drugs (e.g., beta-blockers, phosphodiesterase-5 inhibitors) from the signing of the ICF until 24 weeks after receiving the investigational product, except for protocol-permitted antihypertensive treatments and the investigational product.
28. Any other condition judged by the investigator to make the subject unsuitable for participation in this clinical trial.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Ikke-randomiseret
- Interventionel model: Sekventiel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: 600mg
8 subjects in this cohort will receive the investigational drug ART101 with a dose of 600 mg.
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All participants will receive single subcutaneously of ART101 injection on day 1 .
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Eksperimentel: 800mg
8 subjects in this cohort will receive the investigational drug ART101 with a dose of 800 mg.
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All participants will receive single subcutaneously of ART101 injection on day 1 .
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Vurdér sikkerheden af ART101 ved forekomsten af bivirkninger, bivirkninger af særlig interesse og SAEs
Tidsramme: Op til dag 169 efter første dosisadministration
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Op til dag 169 efter første dosisadministration
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Antal deltagere med unormale laboratorieværdier og/eller bivirkninger, der er relateret til behandlingen
Tidsramme: Op til dag 169 efter første dosering
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Faste serumkemier, faste hematologiske undersøgelser, faste koagulationsanalyser, faste leverfunktionstests, faste lipidpanel, faste glykæmiske vurderinger og urinanalyse vil blive undersøgt.
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Op til dag 169 efter første dosering
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Change in Systolic Blood Pressure (SBP) and Diastolic Blood Pressure(DBP ) measured by 24-hour ambulatory blood pressure monitoring (ABPM) from baseline after single-dose administration;
Tidsramme: 1 time during Screening Period pre dosing , day 22,day 29, Day 43, day 85 and Day 169 post dosing.
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1 time during Screening Period pre dosing , day 22,day 29, Day 43, day 85 and Day 169 post dosing.
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Change in Systolic Blood Pressure (SBP) and Diastolic Blood Pressure(DBP )measured by electronic sphygmomanometer from baseline after single-dose administration;
Tidsramme: Day -1 pre dosing, day 1, day 2, day 3,day 8, day 15, day 22, day 29, day 43, day 57, day 85, day 127, day 169.
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Day -1 pre dosing, day 1, day 2, day 3,day 8, day 15, day 22, day 29, day 43, day 57, day 85, day 127, day 169.
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serum PK Parameters:Maximum Concentration (Cmax)
Tidsramme: Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing.
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Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing.
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Concentration change in pharmacodynamics of ART101 by noting change from baseline of serum angiotensinogen.
Tidsramme: Day -1 pre dosing, day 1, day 3, Day 8, Day 15, Day 22, Day 29, Day 43, Day 57, Day 85 (~3 Months), Day 127, Day 169 (6 Months), post first dose administration.
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Day -1 pre dosing, day 1, day 3, Day 8, Day 15, Day 22, Day 29, Day 43, Day 57, Day 85 (~3 Months), Day 127, Day 169 (6 Months), post first dose administration.
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PK Parameters: Time for maximum concentration (Tmax)
Tidsramme: Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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PK Parameters: Area under the curve (AUC)
Tidsramme: Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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PK Parameters- Elimination half-life (t½)
Tidsramme: Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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PK parameters: Apparent terminal elimination rate (λz )
Tidsramme: Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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PK parameters: Volume of distribution (Vz/F)
Tidsramme: Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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Samples will be collected at 9 timepoints on day 1 including 1 timepoint pre dosing, 1 timepoints on day 2 and 1 timepoint on day 3 post dosing
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Ruihua Dong, Beijing Friendship 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
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- ART101-CN-02
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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