- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07594977
Food-Effect, Single and Multiple Dose Pharmacokinetics, Safety and Tolerability Study of 4-MUST, 128 mg, Tablets in Healthy Volunteers
10. juni 2026 opdateret af: 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.
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
45
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
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Moscow, Rusland, 119991
- Rekruttering
- I.M. Sechenov First Moscow State Medical University
-
Kontakt:
- Elena A Smolyarchuk, MD, PhD
- Telefonnummer: +7 499 248 38 34
- E-mail: smolyarchuk@mail.ru
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ja
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Sekventiel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: 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)
Andre navne:
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Eksperimentel: 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)
Andre navne:
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Eksperimentel: 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)
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Farmakokinetik - AUC-forhold
Tidsramme: Fra 0 til 48 timer (dage 1-3 og 8-10)
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Forholdet mellem arealet under koncentration-tid-kurven over observationstiden og det beregnede areal under koncentration-tid-kurven fra nul til uendelig
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Fra 0 til 48 timer (dage 1-3 og 8-10)
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Farmakokinetik - Cmax/AUC0-t
Tidsramme: Fra 0 til 48 timer (dage 1-3 og 8-10)
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Forholdet mellem den maksimale koncentration og området under koncentration-tid-kurven i observationsperioden
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Fra 0 til 48 timer (dage 1-3 og 8-10)
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Farmakokinetik - f'
Tidsramme: Fra 0 til 48 timer (dage 1-3 og 8-10)
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f' - relativ biotilgængelighed (AUC(0-t)(fodret)/AUC(0-t)(fastende))
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Fra 0 til 48 timer (dage 1-3 og 8-10)
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Farmakokinetik - f''
Tidsramme: Fra 0 til 48 timer (dage 1-3 og 8-10)
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f'' er den relative absorptionshastighed (Cmax(mad)/Cmax(fastende))
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Fra 0 til 48 timer (dage 1-3 og 8-10)
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Pharmacokinetics - Cmax
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Bivirkningstype
Tidsramme: Fra dag -14 - dag -1 (screening) til dag 16 ± 1 (slut af undersøgelsen)
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Bivirkninger vil blive vurderet ved klager, resultater af fysisk undersøgelse, resultater af puls- og blodtryksvurdering, resultater af respirationsfrekvensvurdering, kropstemperatur, laboratorieovervågning (klinisk blodtælling, biokemisk blodtælling, urinanalyse), elektrokardiografi; bivirkninger vil blive klassificeret i overensstemmelse med MedDRA.
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Fra dag -14 - dag -1 (screening) til dag 16 ± 1 (slut af undersøgelsen)
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Hyppighed af uønskede hændelser
Tidsramme: Fra dag -14 - dag -1 (screening) til dag 16 ± 1 (slut af undersøgelsen)
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Antal og hyppighed af uønskede hændelser registreret under undersøgelsen
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Fra dag -14 - dag -1 (screening) til dag 16 ± 1 (slut af undersøgelsen)
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Frafald i forbindelse med uønskede hændelser
Tidsramme: Fra dag -14 - dag -1 (screening) til dag 16 ± 1 (slut af undersøgelsen)
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Antallet af tilfælde af tidlig ophør af deltagelse i undersøgelsen på grund af udviklingen af uønskede hændelser og/eller alvorlige bivirkninger forbundet med undersøgelseslægemidlet
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Fra dag -14 - dag -1 (screening) til dag 16 ± 1 (slut af undersøgelsen)
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Physical examination results - cardiovascular system
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
26. januar 2026
Primær færdiggørelse (Anslået)
30. juni 2027
Studieafslutning (Anslået)
30. juni 2027
Datoer for studieregistrering
Først indsendt
12. maj 2026
Først indsendt, der opfyldte QC-kriterier
12. maj 2026
Først opslået (Faktiske)
19. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
15. juni 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
10. juni 2026
Sidst verificeret
1. juni 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- GIB-01-05-2025
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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