Ta strona została przetłumaczona automatycznie i dokładność tłumaczenia nie jest gwarantowana. Proszę odnieść się do angielska wersja za tekst źródłowy.

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

10 czerwca 2026 zaktualizowane przez: 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.

Przegląd badań

Typ studiów

Interwencyjne

Zapisy (Szacowany)

45

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

      • Moscow, Rosja, 119991
        • Rekrutacyjny
        • I.M. Sechenov First Moscow State Medical University
        • Kontakt:

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Tak

Opis

Inclusion Criteria:

  • Voluntary, personally signed ICF obtained prior to any study procedures;
  • Males and females aged 18 to 45 years (inclusive) of Caucasian race;
  • Confirmed healthy status based on the absence of clinically significant abnormalities in clinical, laboratory, and diagnostic assessments specified in the protocol;
  • Blood pressure (BP): systolic blood pressure (SBP) from 99 to 129 mmHg (inclusive), diastolic blood pressure (DBP) from 70 to 89 mmHg (inclusive);
  • Heart rate (HR) from 60 to 89 beats/min (inclusive);
  • Respiratory rate (RR) from 12 to 20 per 1 minute (inclusive);
  • Body temperature from 36.0°C to 36.9°C (inclusive);
  • Body mass index (BMI) of 18.5 kg/m2 ≤ BMI ≤ 30 kg/m2, with body weight ≥ 55 kg for males and ≥ 45 kg for females;
  • Commitment to adhere to highly effective contraceptive methods during the study participation period and for 30 days thereafter; documentation of negative urine pregnancy test for women of childbearing potential.

Noninclusion Criteria:

  • History of clinically significant allergic reactions;
  • Hypersensitivity to hymecromone and trimebutine and/or excipients included in the study drug in anamnesis;
  • Drug intolerance to hymecromone and trimebutine and/or excipients included in the study drug in the anamnesis;
  • Hereditary galactose intolerance, lactase deficiency or glucose-galactose malabsorption in the anamnesis;
  • Chronic diseases of the kidney, liver, gastrointestinal tract (GIT), cardiovascular, lymphatic, respiratory, nervous, endocrine, musculoskeletal, genitourinary and immune systems, as well as skin, hematopoietic and visual organs;
  • History of GI surgery (except for appendectomy at least 1 year prior to screening);
  • Diseases/conditions that, in the opinion of the investigator, may affect the absorption, distribution, metabolism, or excretion of the study drug;
  • Acute infectious diseases less than 4 weeks prior to screening;
  • Intake of drugs that have a significant effect on hemodynamics and drugs that affect liver function (barbiturates, omeprazole, cimetidine, etc.) less than 2 months before screening;
  • Regular intake of a medicine less than 2 weeks prior to screening and single intake of a medicine less than 7 days prior to screening (including over-the-counter medicines, vitamins, supplements, herbs);
  • Blood or plasma donation less than 3 months prior to screening;
  • Use of hormonal contraceptives (in women) less than 2 months prior to screening;
  • Use of depot injections of any medicine less than 3 months prior to screening;
  • Pregnancy or lactation period; positive pregnancy test for women of childbearing potential;
  • Women of childbearing potential who have had unprotected sexual intercourse with a non-sterilized male partner within 30 days prior to administration of the study drug;
  • Participation in another clinical trial less than 3 months prior to screening or concurrent with the present study;
  • Consumption of more than 10 units of alcohol per week during the month prior to study enrollment (1 unit of alcohol is equivalent to 500 mL of beer, 200 mL of wine, or 50 mL of spirits), or a history of alcoholism, drug dependence, or abuse of medicinal products;
  • Smoking more than 10 cigarettes per day currently, or a history of smoking the indicated number of cigarettes in the 6 months preceding screening; failure to agree to abstain from smoking for the duration of the hospital stay;
  • Consumption of alcohol, caffeine, and xanthine-containing products in the 7 days prior to taking the study drug;
  • Consumption of citrus fruits, cranberries, rose hips and products containing them, preparations or products containing St. John's wort - 7 days before taking the study drug;
  • Dehydration due to diarrhea, vomiting, or other cause within the last 24 hours prior to taking the study drug;
  • Positive blood test result for antibodies to human immunodeficiency virus (HIV) 1 and 2, antibodies to Treponema pallidum antigens, hepatitis B surface antigen (HBsAg), antibodies to hepatitis C virus antigens at screening;
  • Clinically significant abnormalities on electrocardiogram (ECG) in the medical history and/or at screening;
  • Positive urinalysis for narcotics and potent drugs at screening;
  • Positive breath alcohol vapor test at screening;
  • Scheduling a hospital stay during the study period, for any reason other than hospitalization required by this protocol;
  • Failure or inability to comply with protocol requirements, follow protocol procedures, diet and activity regimen.
  • Belonging to a vulnerable population, including: students enrolled in medical, pharmaceutical, or dental educational institutions, clinical and laboratory assistants, pharmaceutical company employees, military personnel and prisoners, persons residing in residential care facilities, low-income and unemployed, minorities, homeless, vagrants, refugees, persons in foster care, persons unable to consent, and law enforcement officers;
  • Any other condition that, in the judgement of the Investigator, would preclude the volunteer's enrollment in the study or could lead to premature withdrawal from the study, including adherence to fasting regimens or special diets (e.g., vegetarian, vegan, or sodium-restricted diets) or lifestyle factors (e.g., night-shift work or extreme physical exertion)

Exclusion criteria:

  • Voluntary withdrawal of the subject from the study;
  • Failure to comply with protocol requirements by the volunteer (e.g., missing scheduled study procedures, unauthorized use of prohibited medications, or violation of dietary or lifestyle restrictions);
  • Occurrence of any event or condition during the study that, in the investigator's judgement, may compromise the volunteer's safety (e.g., hypersensitivity reactions);
  • Volunteers selected for participation in the study in violation of the inclusion/non-inclusion criteria;
  • Development of severe adverse event and/or a serious adverse event in a volunteer during the course of the study;
  • Volunteer is receiving or requires treatment that may affect the pharmacokinetic parameters of the study drug;
  • Missing collection of 2 or more consecutive blood samples or 3 x or more blood samples during the same Study Period;
  • Occurrence of vomiting/diarrhea within 6 h after administration of study drug;
  • Positive urine test for narcotics and potent drugs;
  • Positive breath alcohol test;
  • Positive pregnancy test in women;
  • Occurrence of any other circumstance that precludes conduct of the study in accordance with the protocol.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Inny
  • Przydział: Randomizowane
  • Model interwencyjny: Zadanie sekwencyjne
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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)
Inne nazwy:
  • Siarczan trimebutyny 4-metylobeliferyl
Eksperymentalny: 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)
Inne nazwy:
  • Siarczan trimebutyny 4-metylobeliferyl
Eksperymentalny: 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)
Inne nazwy:
  • Siarczan trimebutyny 4-metylobeliferyl

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Farmakokinetyka - stosunek AUC
Ramy czasowe: Od 0 do 48 godzin (dni 1-3 i 8-10)
Stosunek pola pod krzywą stężenie-czas w czasie obserwacji do obliczonego pola pod krzywą stężenie-czas od zera do nieskończoności
Od 0 do 48 godzin (dni 1-3 i 8-10)
Farmakokinetyka – Cmax/AUC0-t
Ramy czasowe: Od 0 do 48 godzin (dni 1-3 i 8-10)
Stosunek maksymalnego stężenia do pola pod krzywą stężenia w czasie w okresie obserwacji
Od 0 do 48 godzin (dni 1-3 i 8-10)
Farmakokinetyka - f'
Ramy czasowe: Od 0 do 48 godzin (dni 1-3 i 8-10)
f' - biodostępność względna (AUC(0-t)(po posiłku)/AUC(0-t)(na czczo))
Od 0 do 48 godzin (dni 1-3 i 8-10)
Farmakokinetyka - f''
Ramy czasowe: Od 0 do 48 godzin (dni 1-3 i 8-10)
f” to względna szybkość wchłaniania (Cmax (po posiłku)/Cmax (na czczo))
Od 0 do 48 godzin (dni 1-3 i 8-10)
Pharmacokinetics - Cmax
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Rodzaj zdarzenia niepożądanego
Ramy czasowe: Od dnia -14 - dnia -1 (przesiew) do dnia 16 ± 1 (koniec badania)
Zdarzenia niepożądane będą oceniane na podstawie skarg, wyników badania fizykalnego, wyników oceny częstości akcji serca i ciśnienia krwi, wyników oceny częstości oddechów, temperatury ciała, monitorowania laboratoryjnego (morfologia kliniczna, morfologia biochemiczna krwi, analiza moczu), elektrokardiografii; zdarzenia niepożądane będą klasyfikowane zgodnie z MedDRA.
Od dnia -14 - dnia -1 (przesiew) do dnia 16 ± 1 (koniec badania)
Częstotliwość zdarzeń niepożądanych
Ramy czasowe: Od dnia -14 - dnia -1 (przesiew) do dnia 16 ± 1 (koniec badania)
Liczba i częstotliwość zdarzeń niepożądanych zarejestrowanych podczas badania
Od dnia -14 - dnia -1 (przesiew) do dnia 16 ± 1 (koniec badania)
Rezygnacje związane ze zdarzeniami niepożądanymi
Ramy czasowe: Od dnia -14 - dnia -1 (przesiew) do dnia 16 ± 1 (koniec badania)
Liczba przypadków wcześniejszego zakończenia udziału w badaniu ze względu na wystąpienie zdarzeń niepożądanych i/lub poważnych zdarzeń niepożądanych związanych z badanym lekiem
Od dnia -14 - dnia -1 (przesiew) do dnia 16 ± 1 (koniec badania)
Physical examination results - cardiovascular system
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: 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)

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

26 stycznia 2026

Zakończenie podstawowe (Szacowany)

30 czerwca 2027

Ukończenie studiów (Szacowany)

30 czerwca 2027

Daty rejestracji na studia

Pierwszy przesłany

12 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

12 maja 2026

Pierwszy wysłany (Rzeczywisty)

19 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

15 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

10 czerwca 2026

Ostatnia weryfikacja

1 czerwca 2026

Więcej informacji

Terminy związane z tym badaniem

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Subskrybuj