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

10 juni 2026 bijgewerkt door: 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.

Studie Overzicht

Toestand

Werving

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Geschat)

45

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Moscow, Rusland, 119991
        • Werving
        • I.M. Sechenov First Moscow State Medical University
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ander
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Sequentiële toewijzing
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: AB sequence
Cohort 1, Group 1 (sequence AB) will receive 3 tablets (384 mg) of the study drug under fasting conditions in Period I and under fed conditions in Period II.
128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Andere namen:
  • Trimebutine 4-methylumbelliferylsulfaat
Experimenteel: BA sequence
Cohort 1, Group 2 (sequence AB)will receive 3 tablets (384 mg) of the study drug under fed conditions in Period I and under fasting conditions in Period II.
128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Andere namen:
  • Trimebutine 4-methylumbelliferylsulfaat
Experimenteel: Multiple dosing
Cohort 2, Multiple dose: 3 tablets (384 mg) three times daily, 30 minutes before meals, for 3 consecutive days (with the last dose taken in the morning of Day 4).
128 mg tablets containing trimebutine 4-methylumbelliferyl sulfate (4-MUST)
Andere namen:
  • Trimebutine 4-methylumbelliferylsulfaat

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Farmacokinetiek - AUC-ratio
Tijdsspanne: Van 0 tot 48 uur (dag 1-3 en 8-10)
De verhouding van het gebied onder de concentratie-tijdcurve over de observatietijd tot het berekende gebied onder de concentratie-tijdcurve van nul tot oneindig
Van 0 tot 48 uur (dag 1-3 en 8-10)
Farmacokinetiek - Cmax/AUC0-t
Tijdsspanne: Van 0 tot 48 uur (dag 1-3 en 8-10)
De verhouding tussen de maximale concentratie en het gebied onder de concentratie-tijdcurve tijdens de observatieperiode
Van 0 tot 48 uur (dag 1-3 en 8-10)
Farmacokinetiek - f'
Tijdsspanne: Van 0 tot 48 uur (dag 1-3 en 8-10)
f' - relatieve biologische beschikbaarheid (AUC(0-t)(gevoed)/AUC(0-t)(nuchter))
Van 0 tot 48 uur (dag 1-3 en 8-10)
Farmacokinetiek - f''
Tijdsspanne: Van 0 tot 48 uur (dag 1-3 en 8-10)
f'' is de relatieve absorptiesnelheid (Cmax(gevoed)/Cmax(nuchter))
Van 0 tot 48 uur (dag 1-3 en 8-10)
Pharmacokinetics - Cmax
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Maximum plasma concentration (Cmax) of 4-MUST metabolites: trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - tmax
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Time to reach Cmax (tmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - AUC0-t
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Area under the plasma concentration-time curve from time 0 to t (AUC0-t) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - AUC0-inf
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Area under the plasma concentration-time curve from time 0 to infinity (AUC0-inf) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - t1/2
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Elimination half-life (t1/2) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - kel
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Elimination constant (kel) of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - MRT
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Mean residence time (MRT) of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics - Vd
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Volume of distribution of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 48 hours (days 1-3 and 8-10)
Bioavailability - ratio of Cmax
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Ratio of geometric mean Cmax for trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide under fasted and fed conditions (with 90% confidence intervals)
From 0 to 48 hours (days 1-3 and 8-10)
Bioavailability - ratio of AUC0-t
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Ratio of geometric mean AUC0-t for of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide under fasted and fed conditions (with 90% confidence intervals)
From 0 to 48 hours (days 1-3 and 8-10)
Bioavailability - ratio of AUC0-inf
Tijdsspanne: From 0 to 48 hours (days 1-3 and 8-10)
Ratio of geometric mean AUC0-inf for of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide under fasted and fed conditions (with 90% confidence intervals)
From 0 to 48 hours (days 1-3 and 8-10)
Pharmacokinetics (multiple dosing) - number of terminal timepoints
Tijdsspanne: From 72 to 120 hours
number of points in the terminal logarithmic phase used to estimate the terminal elimination rate constant of of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - Cmax
Tijdsspanne: From 72 to 120 hours
Maximum plasma concentration (Cmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - tmax
Tijdsspanne: From 72 to 120 hours
Time to reach Cmax (tmax) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - AUC0-t
Tijdsspanne: From 72 to 120 hours
Area under the plasma concentration-time curve from time 0 to t (AUC0-t) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - AUC0-inf
Tijdsspanne: From 72 to 120 hours
Area under the plasma concentration-time curve from time 0 to infinity (AUC0-inf) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - AUCextr
Tijdsspanne: From 72 to 120 hours
Extrapolated AUC of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - t1/2
Tijdsspanne: From 72 to 120 hours
Elimination half-life (t1/2) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - kel
Tijdsspanne: From 72 to 120 hours
Elimination constant (kel) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - MRT
Tijdsspanne: From 72 to 120 hours
Mean residence time (MRT) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - Vd
Tijdsspanne: From 72 to 120 hours
Volume of distribution of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - CL
Tijdsspanne: From 72 to 120 hours
Clearance (CL) of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 72 to 120 hours
Pharmacokinetics (multiple dosing) - Cmax,ss
Tijdsspanne: From 0 to 72 hours
Maximum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - tmax,ss
Tijdsspanne: From 0 to 72 hours
Time to reach maximum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - tmin,ss
Tijdsspanne: From 0 to 72 hours
Time to reach minimum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - Cmin,ss
Tijdsspanne: From 0 to 72 hours
Minimum plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - Cavg,ss
Tijdsspanne: From 0 to 72 hours
Average plasma concentration at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours
Pharmacokinetics (multiple dosing) - CL,ss
Tijdsspanne: From 0 to 72 hours
Clearance at steady state of trimebutine, N-desmethyltrimebutine, 3,4,5-trimethoxybenzoic acid, 4-methylumbelliferone sulfate, 4-methylumbelliferone and 4-methylumbelliferone glucuronide
From 0 to 72 hours

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Type bijwerking
Tijdsspanne: Van dag -14 - dag -1 (screening) tot dag 16 ± 1 (einde van het onderzoek)
Bijwerkingen worden beoordeeld aan de hand van klachten, resultaten van lichamelijk onderzoek, resultaten van beoordeling van de hartslag en bloeddruk, resultaten van beoordeling van de ademhalingsfrequentie, lichaamstemperatuur, laboratoriummonitoring (klinisch bloedbeeld, biochemisch bloedbeeld, urineonderzoek), elektrocardiografie; Bijwerkingen zullen worden geclassificeerd in overeenstemming met MedDRA.
Van dag -14 - dag -1 (screening) tot dag 16 ± 1 (einde van het onderzoek)
Frequentie van bijwerkingen
Tijdsspanne: Van dag -14 - dag -1 (screening) tot dag 16 ± 1 (einde van het onderzoek)
Aantal en frequentie van bijwerkingen die tijdens het onderzoek zijn geregistreerd
Van dag -14 - dag -1 (screening) tot dag 16 ± 1 (einde van het onderzoek)
Drop-outs geassocieerd met bijwerkingen
Tijdsspanne: Van dag -14 - dag -1 (screening) tot dag 16 ± 1 (einde van het onderzoek)
Het aantal gevallen van vroegtijdige beëindiging van deelname aan het onderzoek als gevolg van de ontwikkeling van bijwerkingen en/of ernstige bijwerkingen die verband houden met het onderzoeksgeneesmiddel
Van dag -14 - dag -1 (screening) tot dag 16 ± 1 (einde van het onderzoek)
Physical examination results - cardiovascular system
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the cardiovascular system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - respiratory system
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the respiratory system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - digestive tract
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the digestive tract on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - endocrine system
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the endocrine system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - musculoskeletal system
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the musculoskeletal system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - nervous system
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the nervous system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - sensory systems
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the sensory systems on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - skin/visible mucous membranes
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the skin/visible mucous membranes on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Physical examination results - genitourinary system
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
An assessment of the condition of the genitourinary system on physical examination (normal condition or list of abnormal conditions, if any)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - systolic blood pressure
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Systolic blood pressure (SBP, mmHg)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - diastolic blood pressure
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Diastolic blood pressure (DBP, mmHg)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - heart rate
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Heart rate (HR, bpm)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - respiratory rate
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Respiratory rate (breaths per minute)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: vital signs - body temperature (Celsius temperature scale)
Tijdsspanne: From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Body temperature (Celsius temperature scale)
From day -14 - day -1 (screening) to day 16 ± 1 (end of the study)
Safety and Tolerability: 12-lead electrocardiogram (ECG) - heart rate
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)

Medewerkers en onderzoekers

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Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

26 januari 2026

Primaire voltooiing (Geschat)

30 juni 2027

Studie voltooiing (Geschat)

30 juni 2027

Studieregistratiedata

Eerst ingediend

12 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

12 mei 2026

Eerst geplaatst (Werkelijk)

19 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

15 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

10 juni 2026

Laatst geverifieerd

1 juni 2026

Meer informatie

Termen gerelateerd aan deze studie

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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