- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07594977
Food-Effect, Single and Multiple Dose Pharmacokinetics, Safety and Tolerability Study of 4-MUST, 128 mg, Tablets in Healthy Volunteers
10. Juni 2026 aktualisiert von: 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.
Studienübersicht
Status
Rekrutierung
Bedingungen
Intervention / Behandlung
Studientyp
Interventionell
Einschreibung (Geschätzt)
45
Phase
- Phase 1
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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-
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Moscow, Russland, 119991
- Rekrutierung
- I.M. Sechenov First Moscow State Medical University
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Kontakt:
- Elena A Smolyarchuk, MD, PhD
- Telefonnummer: +7 499 248 38 34
- E-Mail: smolyarchuk@mail.ru
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Ja
Beschreibung
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.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Sonstiges
- Zuteilung: Zufällig
- Interventionsmodell: Sequenzielle Zuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: AB sequence
Cohort 1, Group 1 (sequence AB) will receive 3 tablets (384 mg) of the study drug under fasting conditions in Period I and under fed conditions in Period II.
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128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Andere Namen:
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Experimental: BA sequence
Cohort 1, Group 2 (sequence AB)will receive 3 tablets (384 mg) of the study drug under fed conditions in Period I and under fasting conditions in Period II.
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128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Andere Namen:
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Experimental: Multiple dosing
Cohort 2, Multiple dose: 3 tablets (384 mg) three times daily, 30 minutes before meals, for 3 consecutive days (with the last dose taken in the morning of Day 4).
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128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Pharmakokinetik – AUC-Verhältnis
Zeitfenster: Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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Das Verhältnis der Fläche unter der Konzentrations-Zeit-Kurve über die Beobachtungszeit zur berechneten Fläche unter der Konzentrations-Zeit-Kurve von Null bis Unendlich
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Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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Pharmakokinetik – Cmax/AUC0-t
Zeitfenster: Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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Das Verhältnis der maximalen Konzentration zur Fläche unter der Konzentrations-Zeit-Kurve während des Beobachtungszeitraums
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Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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Pharmakokinetik - f'
Zeitfenster: Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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f' – relative Bioverfügbarkeit (AUC(0-t)(füttert)/AUC(0-t)(nüchtern))
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Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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Pharmakokinetik - f''
Zeitfenster: Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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f'' ist die relative Absorptionsrate (Cmax(nüchtern)/Cmax(nüchtern))
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Von 0 bis 48 Stunden (Tage 1-3 und 8-10)
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Pharmacokinetics - Cmax
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Art des unerwünschten Ereignisses
Zeitfenster: Von Tag -14 - Tag -1 (Screening) bis Tag 16 ± 1 (Ende der Studie)
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Unerwünschte Ereignisse werden anhand von Beschwerden, Ergebnissen der körperlichen Untersuchung, Ergebnissen der Herzfrequenz- und Blutdruckbeurteilung, Ergebnissen der Atemfrequenzbeurteilung, Körpertemperatur, Laborüberwachung (klinisches Blutbild, biochemisches Blutbild, Urinanalyse), Elektrokardiographie; Unerwünschte Ereignisse werden gemäß MedDRA klassifiziert.
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Von Tag -14 - Tag -1 (Screening) bis Tag 16 ± 1 (Ende der Studie)
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Häufigkeit unerwünschter Ereignisse
Zeitfenster: Von Tag -14 - Tag -1 (Screening) bis Tag 16 ± 1 (Ende der Studie)
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Anzahl und Häufigkeit der während der Studie registrierten unerwünschten Ereignisse
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Von Tag -14 - Tag -1 (Screening) bis Tag 16 ± 1 (Ende der Studie)
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Schulabbrecher im Zusammenhang mit unerwünschten Ereignissen
Zeitfenster: Von Tag -14 - Tag -1 (Screening) bis Tag 16 ± 1 (Ende der Studie)
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Die Anzahl der Fälle eines vorzeitigen Abbruchs der Teilnahme an der Studie aufgrund der Entwicklung unerwünschter Ereignisse und/oder schwerwiegender unerwünschter Ereignisse im Zusammenhang mit dem Studienmedikament
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Von Tag -14 - Tag -1 (Screening) bis Tag 16 ± 1 (Ende der Studie)
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Physical examination results - cardiovascular system
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - heart rate
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
|
Mitarbeiter und Ermittler
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Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
26. Januar 2026
Primärer Abschluss (Geschätzt)
30. Juni 2027
Studienabschluss (Geschätzt)
30. Juni 2027
Studienanmeldedaten
Zuerst eingereicht
12. Mai 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
12. Mai 2026
Zuerst gepostet (Tatsächlich)
19. Mai 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
15. Juni 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
10. Juni 2026
Zuletzt verifiziert
1. Juni 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- GIB-01-05-2025
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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