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Food-Effect, Single and Multiple Dose Pharmacokinetics, Safety and Tolerability Study of 4-MUST, 128 mg, Tablets in Healthy Volunteers

10 juin 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Recrutement

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Estimé)

45

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Moscow, Russie, 119991
        • Recrutement
        • I.M. Sechenov First Moscow State Medical University
        • Contact:
          • Elena A Smolyarchuk, MD, PhD
          • Numéro de téléphone: +7 499 248 38 34
          • E-mail: smolyarchuk@mail.ru

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation séquentielle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.
128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Autres noms:
  • trimebutine 4-méthylumbellifate de sulfate
Expérimental: 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.
128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Autres noms:
  • trimebutine 4-méthylumbellifate de sulfate
Expérimental: 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).
128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Autres noms:
  • trimebutine 4-méthylumbellifate de sulfate

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Pharmacocinétique - rapport AUC
Délai: De 0 à 48 heures (jours 1-3 et 8-10)
Le rapport de l'aire sous la courbe concentration-temps sur la durée d'observation à l'aire calculée sous la courbe concentration-temps de zéro à l'infini.
De 0 à 48 heures (jours 1-3 et 8-10)
Pharmacocinétique - Cmax/ASC0-t
Délai: De 0 à 48 heures (jours 1-3 et 8-10)
Le rapport entre la concentration maximale et l'aire sous la courbe concentration-temps pendant la période d'observation
De 0 à 48 heures (jours 1-3 et 8-10)
Pharmacocinétique - f'
Délai: De 0 à 48 heures (jours 1-3 et 8-10)
f' - biodisponibilité relative (AUC(0-t)(nourri)/AUC(0-t)(à jeun))
De 0 à 48 heures (jours 1-3 et 8-10)
Pharmacocinétique - f''
Délai: De 0 à 48 heures (jours 1-3 et 8-10)
f'' est le taux d'absorption relatif (Cmax(nourri)/Cmax(à jeun))
De 0 à 48 heures (jours 1-3 et 8-10)
Pharmacokinetics - Cmax
Délai: From 0 to 48 hours (days 1-3 and 8-10)
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
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - tmax
Délai: From 0 to 48 hours (days 1-3 and 8-10)
Time to reach Cmax (tmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - AUC0-t
Délai: From 0 to 48 hours (days 1-3 and 8-10)
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
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - AUC0-inf
Délai: From 0 to 48 hours (days 1-3 and 8-10)
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
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - t1/2
Délai: From 0 to 48 hours (days 1-3 and 8-10)
Elimination half-life (t1/2) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - kel
Délai: From 0 to 48 hours (days 1-3 and 8-10)
Elimination constant (kel) of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - MRT
Délai: From 0 to 48 hours (days 1-3 and 8-10)
Mean residence time (MRT) of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - Vd
Délai: From 0 to 48 hours (days 1-3 and 8-10)
Volume of distribution of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Bioavailability - ratio of Cmax
Délai: From 0 to 48 hours (days 1-3 and 8-10)
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)
From 0 to 48 hours (days 1-3 and 8-10)
Bioavailability - ratio of AUC0-t
Délai: From 0 to 48 hours (days 1-3 and 8-10)
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)
From 0 to 48 hours (days 1-3 and 8-10)
Bioavailability - ratio of AUC0-inf
Délai: From 0 to 48 hours (days 1-3 and 8-10)
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)
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics (multiple dosing) - number of terminal timepoints
Délai: From 72 to 120 hours
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
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - Cmax
Délai: From 72 to 120 hours
Maximum plasma concentration (Cmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - tmax
Délai: From 72 to 120 hours
Time to reach Cmax (tmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - AUC0-t
Délai: From 72 to 120 hours
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
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - AUC0-inf
Délai: From 72 to 120 hours
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
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - AUCextr
Délai: From 72 to 120 hours
Extrapolated AUC of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - t1/2
Délai: From 72 to 120 hours
Elimination half-life (t1/2) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - kel
Délai: From 72 to 120 hours
Elimination constant (kel) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - MRT
Délai: From 72 to 120 hours
Mean residence time (MRT) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - Vd
Délai: From 72 to 120 hours
Volume of distribution of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - CL
Délai: From 72 to 120 hours
Clearance (CL) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - Cmax,ss
Délai: From 0 to 72 hours
Maximum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - tmax,ss
Délai: From 0 to 72 hours
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
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - tmin,ss
Délai: From 0 to 72 hours
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
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - Cmin,ss
Délai: From 0 to 72 hours
Minimum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - Cavg,ss
Délai: From 0 to 72 hours
Average plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - CL,ss
Délai: From 0 to 72 hours
Clearance at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Type d'événement indésirable
Délai: Du jour -14 - jour -1 (dépistage) au jour 16 ± 1 (fin de l'étude)
Les événements indésirables seront évalués par les plaintes, les résultats de l'examen physique, les résultats de l'évaluation de la fréquence cardiaque et de la pression artérielle, les résultats de l'évaluation de la fréquence respiratoire, la température corporelle, la surveillance en laboratoire (formule sanguine clinique, formule sanguine biochimique, analyse d'urine), électrocardiographie ; les événements indésirables seront classés conformément à MedDRA.
Du jour -14 - jour -1 (dépistage) au jour 16 ± 1 (fin de l'étude)
Fréquence des événements indésirables
Délai: Du jour -14 - jour -1 (dépistage) au jour 16 ± 1 (fin de l'étude)
Nombre et fréquence des événements indésirables enregistrés au cours de l'étude
Du jour -14 - jour -1 (dépistage) au jour 16 ± 1 (fin de l'étude)
Abandons associés à des événements indésirables
Délai: Du jour -14 - jour -1 (dépistage) au jour 16 ± 1 (fin de l'étude)
Le nombre de cas d'arrêt anticipé de la participation à l'étude en raison du développement d'événements indésirables et/ou d'événements indésirables graves associés au médicament à l'étude
Du jour -14 - jour -1 (dépistage) au jour 16 ± 1 (fin de l'étude)
Physical examination results - cardiovascular system
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the cardiovascular system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - respiratory system
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the respiratory system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - digestive tract
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the digestive tract on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - endocrine system
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the endocrine system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - musculoskeletal system
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the musculoskeletal system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - nervous system
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the nervous system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - sensory systems
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the sensory systems on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - skin/visible mucous membranes
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the skin/visible mucous membranes on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - genitourinary system
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the genitourinary system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - systolic blood pressure
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Systolic blood pressure (SBP, mmHg)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - diastolic blood pressure
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Diastolic blood pressure (DBP, mmHg)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - heart rate
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Heart rate (HR, bpm)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - respiratory rate
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Respiratory rate (breaths per minute)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - body temperature (Celsius temperature scale)
Délai: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Body temperature (Celsius temperature scale)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: 12-lead electrocardiogram (ECG) - heart rate
Délai: 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): heart rate (beats per minute)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: 12-lead electrocardiogram (ECG) - PQ interval
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

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Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

26 janvier 2026

Achèvement primaire (Estimé)

30 juin 2027

Achèvement de l'étude (Estimé)

30 juin 2027

Dates d'inscription aux études

Première soumission

12 mai 2026

Première soumission répondant aux critères de contrôle qualité

12 mai 2026

Première publication (Réel)

19 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

15 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

10 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • GIB-01-05-2025

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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