- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07694843
A Phase I Clinical Trial to Evaluate the Pharmacokinetic and Safety of Ammoxetine Hydrochloride Enteric-Coated Tablets in Participants With Mild Hepatic Impairment, Moderate Hepatic Impairment, and Normal Liver Function
A Phase I Clinical Trial to Evaluate the Pharmacokinetic and Safety of Ammoxetine Hydrochloride Enteric-Coated Tablets in Participants With Mild Hepatic Impairment (Child-Pugh Class A), Moderate Hepatic Impairment (Child-Pugh Class B), and Normal Liver Function
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 1
Kontakter og lokationer
Studiekontakt
- Navn: Clinical Trials Information Group officer
- Telefonnummer: 031169085587
- E-mail: ctr-contact@cspc.cn
Studiesteder
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Jiangsu
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Suzhou, Jiangsu, Kina, 215006
- Rekruttering
- The First Affiliated Hospital Of Soochow University
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Kontakt:
- Miu Liyan, Ph.D
- Telefonnummer: 0512-67972858
- E-mail: miaolysuzhou@163.com
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
Inclusion criteria for participants with abnormal liver function (all 7 criteria must be met):
- Adults aged 18 ~ 75 years (inclusive), regardless of gender
- Body weight ≥ 45.0 kg (female) or ≥ 50.0 kg (male), body mass index (BMI) in the range of 19 ~ 32 kg/m2 (inclusive);
- Participants whose medical history, vital signs, physical examination, laboratory tests (hematology, blood biochemistry, urinalysis, coagulation function, infectious disease screening, and other relevant tests), Chest X-ray, abdominal color Doppler ultrasound, electroencephalogram (EEG), alpha-fetoprotein (AFP), plasma ammonia, abnormal prothrombin, and other examination must be deemed suitable for participation in this study by the investigator;
- Participants and their partners must use effective contraception (e.g., condoms, inert intrauterine devices, etc.) from 2 weeks prior to screening until 6 months after the end of the study, unless they have already undergone permanent sterilization procedures, such as bilateral tubal ligation or vasectomy; furthermore, they must not donate sperm or eggs.
- Participants must have not taken any medications within 2 weeks prior to screening, or must have been on a stable medication regimen for at least 4 weeks for the treatment of liver impairment and/or other comorbidities;
- Participants who have mild or moderate hepatic impairment according to the Child-Pugh classification, resulting from chronic hepatic insufficiency or cirrhosis caused by a history of primary liver disease (e.g., viral hepatitis, alcoholic liver disease, autoimmune hepatitis, etc.), with the investigator determining that the patients liver function would remain stable for ≥1 month based on clinical presentation;
- Participants who voluntarily sign the informed consent form and agree to cooperate in completing the trial according to the protocol.
Inclusion criteria for participants with normal liver function (all 6 criteria must be met):
- Adults aged 18 ~ 75 years (inclusive), regardless of gender(matched for age and gender with the hepatic impairment group);
- Body weight ≥ 45.0 kg (female) or ≥ 50.0 kg (male), body mass index (BMI) in the range of 19 ~ 32 kg/m2 (inclusive);
- Participants whose medical history, vital signs, physical examination, laboratory tests (hematology, blood biochemistry, urinalysis, coagulation function, infectious disease screening, and other relevant tests), Chest X-ray, abdominal color Doppler ultrasound, and other examination must be deemed suitable for participation in this study by the investigator;
- Participants and their partners must use effective contraception (e.g., condoms, inert intrauterine devices, etc.) from 2 weeks prior to screening until 6 months after the end of the study, unless they have already undergone permanent sterilization procedures, such as bilateral tubal ligation or vasectomy; furthermore, they must not donate sperm or eggs.
- Participants must have not taken any medications within 2 weeks prior to screening, or must have been on a stable medication regimen for at least 4 weeks for the treatment of other comorbidities;
- Participants who voluntarily sign the informed consent form and agree to cooperate in completing the trial according to the protocol.
Exclusion Criteria:
Participants meeting any of the following criteria will be excluded from this trial:
- Individuals with a history of allergies (allergic to two or more drugs, foods, or pollens);
- Individuals with major psychiatric disorders, renal disease, neurological disorders, or other systemic diseases that the investigator deems may affect trial results;
- Individuals with orthostatic hypotension (a decrease in systolic blood pressure of 20 mmHg or diastolic blood pressure of 10 mmHg upon standing compared to the supine position);
- Participants with a 12-lead ECG QTcF>470 ms, or those with abnormal ECG findings that the study physician determines may influence the study results, or those with a history of severe arrhythmias, arrhythmia-related syncope, use of a cardiac pacemaker, or other cardiac-related conditions. Conditions include but are not limited to: heart failure; non-sustained or sustained ventricular tachycardia; sick sinus syndrome; or a family history of sudden death;
- Smokers or heavy drinkers within 4 weeks prior to screening (consuming 14 units of alcohol per week: 1 unit = 285 mL of beer, 25 mL of spirits, or 150 mL of wine; smoking ≥5 cigarettes per day) or those with a history of substance or drug abuse within the past year;
- Individuals with a history of dysphagia or any gastrointestinal disease affecting drug absorption;
- Participants with CYP2D6 poor metabolizer;
- Individuals with a positive breathalyzer test for alcohol or a positive urine test for drug abuse during the screening period;
- Individuals who have donated or lost more than 200 mL of blood within 8 weeks prior to screening;
- Participants who have participated in other drug clinical trials within 3 months prior to screening (as determined by the date of administration);
- Individuals who habitually consumed excessive amounts of caffeinated beverages or foods within 4 weeks prior to screening. Examples include coffee, tea, chocolate, cola, and Red Bull (daily caffeine intake should not exceed 6 units).1 caffeine unit = 1 cup of coffee (177.4 mL) = 2 cans of cola (354.9 mL) = 1 cup of tea (354.9 mL) = 1/2 cup of energy drink = 85 g of chocolate;
- Participants who used strong or moderate inhibitors of liver enzymes (CYP2D6) within 4 weeks prior to screening;
- Individuals who have consumed dragon fruit, mango, pomelo, grapefruit, lime, star fruit, pomegranate, or foods or beverages prepared from these fruits within 7 days prior to screening;
- Pregnant or breastfeeding women, or female participants who test positive for pregnancy during the screening period;
- Individuals with estimated glomerular filtration rate (eGFR) < 75 mL/min/1.73 m²calculated using the 2021 CKD-EPI formula based on serum creatinine levels during the screening period;
- Participants with uncontrolled bacterial, viral, parasitic, or fungal infections requiring treatment at screening (excluding hepatitis B), or a history of severe active infection within 1 month prior to screening;
Participants deemed by the investigator to be unsuitable for this clinical trial for other reasons.
Additional exclusion criteria for participants with hepatic impairment (exclusion if any one criterion is met):
- Participants with clinically significant abnormalities in infectious disease screening as determined by the investigator (e.g., patients with active viral hepatitis such as hepatitis B or C) ;
- Participants who have received albumin within 14 days prior to screening;
- Participants with alpha-fetoprotein (AFP) > 40 ng/mL; or hemoglobin (Hb) ≤ 70 g/L; or alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 5 times the upper limit of normal (ULN); or total bilirubin ≥ 5 times the ULN; or platelet count ≤ 30 × 109/L;
- Patients with drug-induced liver injury; within 2 years of liver cancer surgery; history of liver transplantation; acute liver dysfunction due to any cause; patients with diseases affecting bile excretion, such as biliary cirrhosis, biliary obstruction, or cholestatic liver disease; patients with a history of portal-systemic shunt surgery, including transjugular intrahepatic portosystemic shunt (TIPS);
- Patients with a history of any serious disease other than the primary liver disease itself, or a medical history and/or clinically significant abnormal laboratory findings that the investigator believes may affect the trial results, including but not limited to a history of diseases of the circulatory, endocrine, nervous, digestive, or urinary systems, or of hematological, immunological, psychiatric, or metabolic disorders;
Participants with severe complications of cirrhosis who also have any of the following conditions: active bleeding from ruptured esophageal or fundic varices; severe or advanced ascites or pleural effusion requiring paracentesis, drainage, and albumin supplementation; participants with hepatorenal syndrome; overt hepatic encephalopathy; liver failure; or other conditions deemed by the investigator to render the participant unsuitable for the study;
Additional exclusion criteria for participants with normal liver function (exclusion if any one criterion is met):
- Participants with a history of liver dysfunction, or physical examination and laboratory tests at screening indicating the presence or possible presence of liver dysfunction;
- Participants who have a positive result for hepatitis B surface antigen (HBsAg) or any hepatitis C virus antibody test.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Mild hepatic impairment Group
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Oral administration; 20 mg
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Eksperimentel: Moderate hepatic impairment Group
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Oral administration; 20 mg
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Eksperimentel: Normal hepatic function Group
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Oral administration; 20 mg
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Area under the concentration vs. time curve for one dosing interval at steady-state (AUCtau,ss)
Tidsramme: Within 120 hours after the last dose
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Within 120 hours after the last dose
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Maximum concentration observed during dosing interval at steady-state (Cmax,ss)
Tidsramme: Within 120 hours after the last dose
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Within 120 hours after the last dose
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
The incidence of adverse events (AEs)
Tidsramme: Up to 120 hours after the last dose
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Up to 120 hours after the last dose
|
|
Minimum concentration observed during dosing interval at steady-state (Cmin,ss)
Tidsramme: Up to 120 hours after the last dose
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Up to 120 hours after the last dose
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Half-Life (t1/2)
Tidsramme: Up to 120 hours after the last dose
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Up to 120 hours after the last dose
|
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Mean concentration observed during dosing interval at steady-state (Cav,ss)
Tidsramme: Up to 120 hours after the last dose
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Up to 120 hours after the last dose
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Plasma Maximum concentration (Cmax)
Tidsramme: Within 24 hours after the first dose
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Within 24 hours after the first dose
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Area under the concentration-time curve up to the last sampling point(AUClast)
Tidsramme: Within 24 hours after the first dose
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Within 24 hours after the first dose
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Accumulation index of AUC(RAUC)
Tidsramme: Within 24 hours after the first dose
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Within 24 hours after the first dose
|
Samarbejdspartnere og efterforskere
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
Andre undersøgelses-id-numre
- HA1406-012
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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