- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07594977
Food-Effect, Single and Multiple Dose Pharmacokinetics, Safety and Tolerability Study of 4-MUST, 128 mg, Tablets in Healthy Volunteers
10 juni 2026 uppdaterad av: 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.
Studieöversikt
Status
Rekrytering
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
45
Fas
- Fas 1
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
-
Moscow, Ryssland, 119991
- Rekrytering
- I.M. Sechenov First Moscow State Medical University
-
Kontakt:
- Elena A Smolyarchuk, MD, PhD
- Telefonnummer: +7 499 248 38 34
- E-post: smolyarchuk@mail.ru
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
Tar emot friska volontärer
Ja
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Övrig
- Tilldelning: Randomiserad
- Interventionsmodell: Sekventiell tilldelning
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: 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)
Andra namn:
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Experimentell: 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)
Andra namn:
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Experimentell: 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)
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Farmakokinetik - AUC-förhållande
Tidsram: Från 0 till 48 timmar (dag 1-3 och 8-10)
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Förhållandet mellan arean under koncentration-tid-kurvan över observationstiden och den beräknade arean under koncentration-tid-kurvan från noll till oändlighet
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Från 0 till 48 timmar (dag 1-3 och 8-10)
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Farmakokinetik - Cmax/AUC0-t
Tidsram: Från 0 till 48 timmar (dag 1-3 och 8-10)
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Förhållandet mellan den maximala koncentrationen och området under koncentration-tid-kurvan under observationsperioden
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Från 0 till 48 timmar (dag 1-3 och 8-10)
|
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Farmakokinetik - f'
Tidsram: Från 0 till 48 timmar (dag 1-3 och 8-10)
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f' - relativ biotillgänglighet (AUC(0-t)(matad)/AUC(0-t)(fastande))
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Från 0 till 48 timmar (dag 1-3 och 8-10)
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Farmakokinetik - f''
Tidsram: Från 0 till 48 timmar (dag 1-3 och 8-10)
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f'' är den relativa absorptionshastigheten (Cmax(matad)/Cmax(fastande))
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Från 0 till 48 timmar (dag 1-3 och 8-10)
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Pharmacokinetics - Cmax
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
|
|
Pharmacokinetics (multiple dosing) - CL,ss
Tidsram: 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
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From 0 to 72 hours
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Typ av biverkning
Tidsram: Från dag -14 - dag -1 (screening) till dag 16 ± 1 (slutet av studien)
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Biverkningar kommer att bedömas genom klagomål, resultat av fysisk undersökning, resultat av hjärtfrekvens och blodtrycksbedömning, resultat av andningsfrekvensbedömning, kroppstemperatur, laboratorieövervakning (kliniskt blodvärde, biokemiskt blodvärde, urinanalys), elektrokardiografi; biverkningar kommer att klassificeras i enlighet med MedDRA.
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Från dag -14 - dag -1 (screening) till dag 16 ± 1 (slutet av studien)
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Biverkningsfrekvens
Tidsram: Från dag -14 - dag -1 (screening) till dag 16 ± 1 (slutet av studien)
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Antal och frekvens av biverkningar som registrerats under studien
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Från dag -14 - dag -1 (screening) till dag 16 ± 1 (slutet av studien)
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Avhopp i samband med biverkningar
Tidsram: Från dag -14 - dag -1 (screening) till dag 16 ± 1 (slutet av studien)
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Antalet fall av tidigt avbrutet deltagande i studien på grund av utvecklingen av biverkningar och/eller allvarliga biverkningar associerade med studieläkemedlet
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Från dag -14 - dag -1 (screening) till dag 16 ± 1 (slutet av studien)
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Physical examination results - cardiovascular system
Tidsram: 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
Tidsram: 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
Tidsram: 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)
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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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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)
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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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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)
Tidsram: 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
Tidsram: 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)
|
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - PQ interval
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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)
|
Samarbetspartners och utredare
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Sponsor
Studieavstämningsdatum
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Studera stora datum
Studiestart (Faktisk)
26 januari 2026
Primärt slutförande (Beräknad)
30 juni 2027
Avslutad studie (Beräknad)
30 juni 2027
Studieregistreringsdatum
Först inskickad
12 maj 2026
Först inskickad som uppfyllde QC-kriterierna
12 maj 2026
Första postat (Faktisk)
19 maj 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
15 juni 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
10 juni 2026
Senast verifierad
1 juni 2026
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- GIB-01-05-2025
Läkemedels- och apparatinformation, studiedokument
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Nej
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