- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07594977
Food-Effect, Single and Multiple Dose Pharmacokinetics, Safety and Tolerability Study of 4-MUST, 128 mg, Tablets in Healthy Volunteers
10 de junho de 2026 atualizado por: Valenta Pharm JSC
An Open-Label Study to Evaluate the Effect of Food on the Bioavailability of 4-MUST, 128 mg, Tablets and to Assess the Pharmacokinetics, Safety, and Tolerability Following Single and Multiple Dose Administration in Healthy Volunteers
This open-label study will evaluate the effect of food on the bioavailability of a single dose of 4-MUST, tablets, 128 mg.
Additionally, the study will assess the pharmacokinetics, safety, and tolerability of 4-MUST, tablets, 128 mg following both single and multiple oral dose administration.
Visão geral do estudo
Status
Recrutamento
Condições
Intervenção / Tratamento
Tipo de estudo
Intervencional
Inscrição (Estimado)
45
Estágio
- Fase 1
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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-
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Moscow, Rússia, 119991
- Recrutamento
- I.M. Sechenov First Moscow State Medical University
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Contato:
- Elena A Smolyarchuk, MD, PhD
- Número de telefone: +7 499 248 38 34
- E-mail: smolyarchuk@mail.ru
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Sim
Descrição
Inclusion Criteria:
- Voluntary, personally signed ICF obtained prior to any study procedures;
- Males and females aged 18 to 45 years (inclusive) of Caucasian race;
- Confirmed healthy status based on the absence of clinically significant abnormalities in clinical, laboratory, and diagnostic assessments specified in the protocol;
- Blood pressure (BP): systolic blood pressure (SBP) from 99 to 129 mmHg (inclusive), diastolic blood pressure (DBP) from 70 to 89 mmHg (inclusive);
- Heart rate (HR) from 60 to 89 beats/min (inclusive);
- Respiratory rate (RR) from 12 to 20 per 1 minute (inclusive);
- Body temperature from 36.0°C to 36.9°C (inclusive);
- Body mass index (BMI) of 18.5 kg/m2 ≤ BMI ≤ 30 kg/m2, with body weight ≥ 55 kg for males and ≥ 45 kg for females;
- Commitment to adhere to highly effective contraceptive methods during the study participation period and for 30 days thereafter; documentation of negative urine pregnancy test for women of childbearing potential.
Noninclusion Criteria:
- History of clinically significant allergic reactions;
- Hypersensitivity to hymecromone and trimebutine and/or excipients included in the study drug in anamnesis;
- Drug intolerance to hymecromone and trimebutine and/or excipients included in the study drug in the anamnesis;
- Hereditary galactose intolerance, lactase deficiency or glucose-galactose malabsorption in the anamnesis;
- Chronic diseases of the kidney, liver, gastrointestinal tract (GIT), cardiovascular, lymphatic, respiratory, nervous, endocrine, musculoskeletal, genitourinary and immune systems, as well as skin, hematopoietic and visual organs;
- History of GI surgery (except for appendectomy at least 1 year prior to screening);
- Diseases/conditions that, in the opinion of the investigator, may affect the absorption, distribution, metabolism, or excretion of the study drug;
- Acute infectious diseases less than 4 weeks prior to screening;
- Intake of drugs that have a significant effect on hemodynamics and drugs that affect liver function (barbiturates, omeprazole, cimetidine, etc.) less than 2 months before screening;
- Regular intake of a medicine less than 2 weeks prior to screening and single intake of a medicine less than 7 days prior to screening (including over-the-counter medicines, vitamins, supplements, herbs);
- Blood or plasma donation less than 3 months prior to screening;
- Use of hormonal contraceptives (in women) less than 2 months prior to screening;
- Use of depot injections of any medicine less than 3 months prior to screening;
- Pregnancy or lactation period; positive pregnancy test for women of childbearing potential;
- Women of childbearing potential who have had unprotected sexual intercourse with a non-sterilized male partner within 30 days prior to administration of the study drug;
- Participation in another clinical trial less than 3 months prior to screening or concurrent with the present study;
- Consumption of more than 10 units of alcohol per week during the month prior to study enrollment (1 unit of alcohol is equivalent to 500 mL of beer, 200 mL of wine, or 50 mL of spirits), or a history of alcoholism, drug dependence, or abuse of medicinal products;
- Smoking more than 10 cigarettes per day currently, or a history of smoking the indicated number of cigarettes in the 6 months preceding screening; failure to agree to abstain from smoking for the duration of the hospital stay;
- Consumption of alcohol, caffeine, and xanthine-containing products in the 7 days prior to taking the study drug;
- Consumption of citrus fruits, cranberries, rose hips and products containing them, preparations or products containing St. John's wort - 7 days before taking the study drug;
- Dehydration due to diarrhea, vomiting, or other cause within the last 24 hours prior to taking the study drug;
- Positive blood test result for antibodies to human immunodeficiency virus (HIV) 1 and 2, antibodies to Treponema pallidum antigens, hepatitis B surface antigen (HBsAg), antibodies to hepatitis C virus antigens at screening;
- Clinically significant abnormalities on electrocardiogram (ECG) in the medical history and/or at screening;
- Positive urinalysis for narcotics and potent drugs at screening;
- Positive breath alcohol vapor test at screening;
- Scheduling a hospital stay during the study period, for any reason other than hospitalization required by this protocol;
- Failure or inability to comply with protocol requirements, follow protocol procedures, diet and activity regimen.
- Belonging to a vulnerable population, including: students enrolled in medical, pharmaceutical, or dental educational institutions, clinical and laboratory assistants, pharmaceutical company employees, military personnel and prisoners, persons residing in residential care facilities, low-income and unemployed, minorities, homeless, vagrants, refugees, persons in foster care, persons unable to consent, and law enforcement officers;
- Any other condition that, in the judgement of the Investigator, would preclude the volunteer's enrollment in the study or could lead to premature withdrawal from the study, including adherence to fasting regimens or special diets (e.g., vegetarian, vegan, or sodium-restricted diets) or lifestyle factors (e.g., night-shift work or extreme physical exertion)
Exclusion criteria:
- Voluntary withdrawal of the subject from the study;
- Failure to comply with protocol requirements by the volunteer (e.g., missing scheduled study procedures, unauthorized use of prohibited medications, or violation of dietary or lifestyle restrictions);
- Occurrence of any event or condition during the study that, in the investigator's judgement, may compromise the volunteer's safety (e.g., hypersensitivity reactions);
- Volunteers selected for participation in the study in violation of the inclusion/non-inclusion criteria;
- Development of severe adverse event and/or a serious adverse event in a volunteer during the course of the study;
- Volunteer is receiving or requires treatment that may affect the pharmacokinetic parameters of the study drug;
- Missing collection of 2 or more consecutive blood samples or 3 x or more blood samples during the same Study Period;
- Occurrence of vomiting/diarrhea within 6 h after administration of study drug;
- Positive urine test for narcotics and potent drugs;
- Positive breath alcohol test;
- Positive pregnancy test in women;
- Occurrence of any other circumstance that precludes conduct of the study in accordance with the protocol.
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Outro
- Alocação: Randomizado
- Modelo Intervencional: Atribuição sequencial
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
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Experimental: AB sequence
Cohort 1, Group 1 (sequence AB) will receive 3 tablets (384 mg) of the study drug under fasting conditions in Period I and under fed conditions in Period II.
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128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Outros nomes:
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Experimental: BA sequence
Cohort 1, Group 2 (sequence AB)will receive 3 tablets (384 mg) of the study drug under fed conditions in Period I and under fasting conditions in Period II.
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128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Outros nomes:
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Experimental: Multiple dosing
Cohort 2, Multiple dose: 3 tablets (384 mg) three times daily, 30 minutes before meals, for 3 consecutive days (with the last dose taken in the morning of Day 4).
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128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Farmacocinética - relação AUC
Prazo: De 0 a 48 horas (dias 1-3 e 8-10)
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A razão entre a área sob a curva concentração-tempo durante o tempo de observação e a área calculada sob a curva concentração-tempo de zero ao infinito
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De 0 a 48 horas (dias 1-3 e 8-10)
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Farmacocinética – Cmax/AUC0-t
Prazo: De 0 a 48 horas (dias 1-3 e 8-10)
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A razão entre a concentração máxima e a área sob a curva concentração-tempo durante o período de observação
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De 0 a 48 horas (dias 1-3 e 8-10)
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Farmacocinética - f'
Prazo: De 0 a 48 horas (dias 1-3 e 8-10)
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f' - biodisponibilidade relativa (AUC(0-t)(alimentado)/AUC(0- t)(jejum))
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De 0 a 48 horas (dias 1-3 e 8-10)
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Farmacocinética - f''
Prazo: De 0 a 48 horas (dias 1-3 e 8-10)
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f'' é a taxa de absorção relativa (Cmax(alimentado)/Cmax(jejum))
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De 0 a 48 horas (dias 1-3 e 8-10)
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Pharmacokinetics - Cmax
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Maximum plasma concentration (Cmax) of 4-MUST metabolites: trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics - tmax
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Time to reach Cmax (tmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics - AUC0-t
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Area under the plasma concentration-time curve from time 0 to t (AUC0-t) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics - AUC0-inf
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Area under the plasma concentration-time curve from time 0 to infinity (AUC0-inf) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics - t1/2
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Elimination half-life (t1/2) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics - kel
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Elimination constant (kel) of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics - MRT
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Mean residence time (MRT) of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics - Vd
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Volume of distribution of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 48 hours (days 1-3 and 8-10)
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Bioavailability - ratio of Cmax
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Ratio of geometric mean Cmax for trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide under fasted and fed conditions (with 90% confidence intervals)
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From 0 to 48 hours (days 1-3 and 8-10)
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Bioavailability - ratio of AUC0-t
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Ratio of geometric mean AUC0-t for of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide under fasted and fed conditions (with 90% confidence intervals)
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From 0 to 48 hours (days 1-3 and 8-10)
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Bioavailability - ratio of AUC0-inf
Prazo: From 0 to 48 hours (days 1-3 and 8-10)
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Ratio of geometric mean AUC0-inf for of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide under fasted and fed conditions (with 90% confidence intervals)
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From 0 to 48 hours (days 1-3 and 8-10)
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Pharmacokinetics (multiple dosing) - number of terminal timepoints
Prazo: From 72 to 120 hours
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number of points in the terminal logarithmic phase used to estimate the terminal elimination rate constant of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - Cmax
Prazo: From 72 to 120 hours
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Maximum plasma concentration (Cmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - tmax
Prazo: From 72 to 120 hours
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Time to reach Cmax (tmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - AUC0-t
Prazo: From 72 to 120 hours
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Area under the plasma concentration-time curve from time 0 to t (AUC0-t) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - AUC0-inf
Prazo: From 72 to 120 hours
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Area under the plasma concentration-time curve from time 0 to infinity (AUC0-inf) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - AUCextr
Prazo: From 72 to 120 hours
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Extrapolated AUC of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - t1/2
Prazo: From 72 to 120 hours
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Elimination half-life (t1/2) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - kel
Prazo: From 72 to 120 hours
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Elimination constant (kel) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - MRT
Prazo: From 72 to 120 hours
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Mean residence time (MRT) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - Vd
Prazo: From 72 to 120 hours
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Volume of distribution of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - CL
Prazo: From 72 to 120 hours
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Clearance (CL) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 72 to 120 hours
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Pharmacokinetics (multiple dosing) - Cmax,ss
Prazo: From 0 to 72 hours
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Maximum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 72 hours
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Pharmacokinetics (multiple dosing) - tmax,ss
Prazo: From 0 to 72 hours
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Time to reach maximum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 72 hours
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Pharmacokinetics (multiple dosing) - tmin,ss
Prazo: From 0 to 72 hours
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Time to reach minimum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 72 hours
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Pharmacokinetics (multiple dosing) - Cmin,ss
Prazo: From 0 to 72 hours
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Minimum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 72 hours
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Pharmacokinetics (multiple dosing) - Cavg,ss
Prazo: From 0 to 72 hours
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Average plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 72 hours
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Pharmacokinetics (multiple dosing) - CL,ss
Prazo: From 0 to 72 hours
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Clearance at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
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From 0 to 72 hours
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Tipo de evento adverso
Prazo: Do dia -14 - dia -1 (triagem) ao dia 16 ± 1 (final do estudo)
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Os eventos adversos serão avaliados por meio de queixas, resultados de exame físico, resultados de avaliação de frequência cardíaca e pressão arterial, resultados de avaliação de frequência respiratória, temperatura corporal, monitoramento laboratorial (hemograma clínico, hemograma bioquímico, urinálise), eletrocardiografia; os eventos adversos serão classificados de acordo com MedDRA.
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Do dia -14 - dia -1 (triagem) ao dia 16 ± 1 (final do estudo)
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Frequência de eventos adversos
Prazo: Do dia -14 - dia -1 (triagem) ao dia 16 ± 1 (final do estudo)
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Número e frequência de eventos adversos registrados durante o estudo
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Do dia -14 - dia -1 (triagem) ao dia 16 ± 1 (final do estudo)
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Desistências associadas a eventos adversos
Prazo: Do dia -14 - dia -1 (triagem) ao dia 16 ± 1 (final do estudo)
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O número de casos de encerramento antecipado da participação no estudo devido ao desenvolvimento de eventos adversos e/ou eventos adversos graves associados ao medicamento em estudo
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Do dia -14 - dia -1 (triagem) ao dia 16 ± 1 (final do estudo)
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Physical examination results - cardiovascular system
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the cardiovascular system on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - respiratory system
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the respiratory system on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - digestive tract
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the digestive tract on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - endocrine system
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the endocrine system on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - musculoskeletal system
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the musculoskeletal system on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - nervous system
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the nervous system on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - sensory systems
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the sensory systems on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - skin/visible mucous membranes
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the skin/visible mucous membranes on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Physical examination results - genitourinary system
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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An assessment of the condition of the genitourinary system on physical examination (normal condition or list of abnormal conditions, if any)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Safety and Tolerability: vital signs - systolic blood pressure
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Systolic blood pressure (SBP, mmHg)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Safety and Tolerability: vital signs - diastolic blood pressure
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Diastolic blood pressure (DBP, mmHg)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Safety and Tolerability: vital signs - heart rate
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Heart rate (HR, bpm)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Safety and Tolerability: vital signs - respiratory rate
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Respiratory rate (breaths per minute)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Safety and Tolerability: vital signs - body temperature (Celsius temperature scale)
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Body temperature (Celsius temperature scale)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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Safety and Tolerability: 12-lead electrocardiogram (ECG) - heart rate
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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12-lead ECG (I, II, III, aVR-enhanced unipolar abduction from the right arm , aVL-enhanced unipolar abduction from the left arm, aVF - enhanced unipolar abduction from the left leg, V1-V6): heart rate (beats per minute)
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From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
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|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - PQ interval
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
12-lead ECG (I, II, III, aVR-enhanced unipolar abduction from the right arm , aVL-enhanced unipolar abduction from the left arm, aVF - enhanced unipolar abduction from the left leg, V1-V6): PQ interval (is the period, measured in milliseconds, that extends from the beginning of the P wave (the onset of atrial depolarization) until the beginning of the QRS complex)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - QRS complex
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
12-lead ECG (I, II, III, aVR-enhanced unipolar abduction from the right arm , aVL-enhanced unipolar abduction from the left arm, aVF - enhanced unipolar abduction from the left leg, V1-V6) taken while lying down: QRS complex (the QRS complex is the combination of three of the graphical deflections seen on a typical electrocardiogram)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - QT interval
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
12-lead ECG (I, II, III, aVR-enhanced unipolar abduction from the right arm , aVL-enhanced unipolar abduction from the left arm, aVF - enhanced unipolar abduction from the left leg, V1-V6) taken while lying down: QT interval (distance from the beginning of the QRS complex to the end of the T wave)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - hemoglobin
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Hemoglobin (g/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - hematocrit
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Hematocrit (%)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - red blood cell count
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Red blood cell count (cells/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - platelet count
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Platelet count (cells/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - leukocyte count
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte count (cells/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - erythrocyte sedimentation rate
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Erythrocyte sedimentation rate (mm/h)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - myelocytes
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte formula (myelocytes, %)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - band neutrophils
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte formula (band neutrophils, %)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - segmented neutrophils
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte formula (segmented neutrophils, %)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - eosinophils
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte formula (eosinophils, %)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - basophils
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte formula (basophils, %)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - monocytes
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte formula (monocytes, %)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: clinical blood test - lymphocytes
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Leukocyte formula (lymphocytes, %)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - glucose
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Glucose concentration (mmol/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - cholesterol
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Total cholesterol concentration (mmol/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - total protein
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Total protein in blood serum (g/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - bilirubin
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Total bilirubin concentration (micromol/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - creatinine
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Creatinine concentration (micromol/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - alkaline phosphatase
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Alkaline phosphatase activity (U/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - alanine transaminase
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Alanine transaminase activity (U/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: blood chemistry - aspartate transaminase
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Aspartate transaminase activity (U/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - specific gravity
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Specific gravity of the urine
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - color
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Color of the urine
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - transparency
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Transparency of the urine
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - pH
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
pH of the urine
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - protein
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Protein concentration (g/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - glucose
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Glucose concentration (mmol/L)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - red blood cells
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Red blood cell content (number in sight)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - white blood cells
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
White blood cell content (number in sight)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - casts
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Presence of casts (Yes/No)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - mucus
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Presence of mucus (Yes/No)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: urinalysis - bacteria
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Presence of bacteria (Yes/No)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Adverse event severety
Prazo: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Severity of adverse events registered during the study, assessed using the Common Terminology Criteria for Adverse Events (CTCAE)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
26 de janeiro de 2026
Conclusão Primária (Estimado)
30 de junho de 2027
Conclusão do estudo (Estimado)
30 de junho de 2027
Datas de inscrição no estudo
Enviado pela primeira vez
12 de maio de 2026
Enviado pela primeira vez que atendeu aos critérios de CQ
12 de maio de 2026
Primeira postagem (Real)
19 de maio de 2026
Atualizações de registro de estudo
Última Atualização Postada (Real)
15 de junho de 2026
Última atualização enviada que atendeu aos critérios de controle de qualidade
10 de junho de 2026
Última verificação
1 de junho de 2026
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- GIB-01-05-2025
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Não
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Não
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .