- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07645534
Safety and Pharmacokinetics of Ingavirin Forte, Capsules, 90 mg + 20 mg (Valenta Pharm JSC, Russia) Compared With Ingavirin, Capsules, 90 mg, Under Fasting and Fed Conditions.
11. juni 2026 opdateret af: Valenta Pharm JSC
An Open-Label, Randomized, Crossover Clinical Study to Evaluate the Safety and Pharmacokinetics of the Active Ingredients of Ingavirin Forte, Capsules, 90 mg + 20 mg (Valenta Pharm JSC, Russia) Fixed-Dose Combination Compared With Single-Ingredient Drug Ingavirin, Capsules, 90 mg Under Fasting and Fed Conditions.
This study aims to evaluate the safety and pharmacokinetic profile of the active ingredients Ingavirin forte, capsules, 90 mg + 20 mg (Valenta Pharm JSC, Russia) relative to single-entity Drug Ingavirin, capsules, 90 mg following administration under fasting and fed conditions.
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
36
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
Saint Petersburg, Rusland, 191036
- Rekruttering
- Federal Budgetary Institution of Science "North-West Public Health Research Center"
-
Kontakt:
- Elena Shalukho, MD
- Telefonnummer: +7 (903) 099 57 86
- E-mail: Elena.Shalukho@yandex.ru
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Voluntarily and personally signed Informed Consent Form (ICF) by a participant obtained prior to the conduct of any study-related procedure;
- Males and females aged 18 to 45 years (inclusive);
- Confirmed healthy status, defined as the absence of clinically significant abnormalities based on clinical evaluation, laboratory assessments, and diagnostic procedures as specified in the protocol;
- Blood pressure (BP) level: systolic blood pressure (SBP) from 100 to 130 mmHg (inclusive), diastolic blood pressure (DBP) from 70 to 85 mmHg (inclusive);
- Heart rate (HR) from 60 to 89 beats/min (inclusive);
- Respiratory rate (RR) from 12 to 20 per 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 for men being ≥ 55 kg and for women ≥ 45 kg;
- Agreement to use adequate methods of contraception throughout the study and for 30 days after its completion; for women of childbearing potential - a negative urine β-hCG test result;
- Subjects must demonstrate appropriate behavior and coherent speech;
- Ability to comply with the daily routine and diet prescribed by the study protocol.
Noninclusion Criteria:
- Clinically significant allergic history;
- History of hypersensitivity to imidazolylethanamide of pentanedioic acid and N,N'-bis-[2-(1,3-diazocyclopenta-2,4-dien-4-yl)ethyl] diamide of malonic acid (XC9) and/or to the excipients contained in the investigational medicinal product;
- History of drug intolerance to imidazolylethanamide of pentanedioic acid and N,N'-bis-[2-(1,3-diazocyclopenta-2,4-dien-4-yl)ethyl] diamide of malonic acid (XC9) and/or to the excipients contained in the investigational medicinal product;
- Known galactose intolerance, lactase deficiency, or glucose-galactose malabsorption;
- Chronic diseases of the kidneys, liver, gastrointestinal (GI) tract, cardiovascular, lymphatic, respiratory, nervous, endocrine, musculoskeletal, genitourinary, or immune systems, or of the skin, hematopoietic organs, or eyes;
- History of gastrointestinal (GI) surgical procedures, with the exception of appendectomy performed at least 1 year prior to screening;
- Diseases/conditions that, in the investigator's opinion, may affect the absorption, distribution, metabolism, or excretion of the investigational medicinal product (IMP);
- Acute infectious diseases less than 4 weeks prior to screening;
- Use of medicinal products (MPs) that have a pronounced effect on hemodynamics, MPs affecting liver function (barbiturates, omeprazole, cimetidine, etc.), MPs prolonging the QT interval (antipsychotics (haloperidol, quetiapine, olanzapine, risperidone, sulpiride), antidepressants (fluoxetine, sertraline), antiarrhythmics (amiodarone), antibiotics (clarithromycin, azithromycin, moxifloxacin, levofloxacin, ciprofloxacin), antifungals (fluconazole), diuretics (furosemide)) less than 2 months prior to screening;
- Regular use of MPs less than 2 weeks prior to screening and single use of MPs less than 7 days prior to screening (including over-the-counter MPs, vitamins, dietary supplements, herbal medicinal products);
- Donation of blood or plasma less than 3 months prior to screening;
- Use of hormonal contraceptives by womeninitiated less than 2 months prior to the screening visit.
- Use of depot injections of any MPs less than 3 months prior to the start of screening;
- Pregnancy or breastfeeding; positive urine pregnancy test result for women of childbearing potential;
- Women of childbearing potential with a history of unprotected sexual intercourse within 30 days prior to study drug administration with a non-sterilized partner;
- Participation in another clinical trial within 3 months prior to screening or concurrently with the current study.
- Consumption of more than 10 standard alcohol units per week during the month prior to study enrollment, (1 standard unit = 500 mL beer, 200 mL wine, or 50 mL of strong alcoholic beverages), or history of alcoholism, drug dependence, or substance abuse.
- Currently smoking more than 10 cigarettes per day, or a history of smoking the specified number of cigarettes within the 6 months preceding screening; refusal to abstain from smoking while staying at the study center;
- Consumption of alcohol, caffeine, and xanthine-containing products within 7 days prior to IMP administration;
- Consumption of citrus fruits, cranberries, rose hips and products containing them, or St. John's wort-containing preparations or products within 7 days prior to IMP administration;
- Dehydration due to diarrhea, vomiting, or other causes within the last 24 hours prior to IMP administration;
- Positive blood test result for antibodies to human immunodeficiency virus (HIV) 1 and 2, antibodies to Treponema pallidum antigens, hepatitis B surface antigen (HBsAg), or antibodies to hepatitis C virus antigens at screening;
- Clinically significant abnormalities on the electrocardiogram (ECG) in the medical history and/or at screening, including: QTcF interval (corrected by Fredericia) ≥430 ms in men and ≥450 ms in women;
- History of risk factors for torsades de pointes, such as heart failure, hypokalemia, or family history of long QT syndrome;
- Electrolyte imbalances (based on Na+, K+, Cl- levels at screening);
- Positive urine test for narcotic substances and potent medicinal products at screening;
- Positive breath alcohol test at screening;
- Planned hospitalization during the study period for any reason other than hospitalization required by this protocol;
- Inability or incapacity to comply with the protocol requirements, perform protocol-specified procedures, or adhere to the diet and activity restrictions;
- Belonging to a vulnerable group of volunteers: students of higher and secondary medical, pharmaceutical, and dental educational institutions; subordinate clinical or laboratory staff; employees of pharmaceutical companies; military personnel and prisoners; residents of long-term care facilities; low-income and unemployed individuals; representatives of national minorities; homeless individuals; refugees; individuals under guardianship or trusteeship; persons incapable of providing informed consent; as well as law enforcement officers;
- Any other condition which, in the Investigator's judgment, would preclude the subject's enrollment in the study or could lead to premature withdrawal, including adherence to fasting practices or special diets (e.g., vegetarian, vegan, sodium-restricted) or lifestyle factors (e.g., night shift work, extreme physical exertion).
Exclusion criteria:
- Subject's decision to discontinue participation in the study;
- Subject non-compliance with protocol requirements, including but not limited to missed study procedures, unauthorized use of prohibited concomitant medications, or failure to adhere to protocol-defined dietary and lifestyle restrictions.
- Occurrence of any medical condition or safety concern during study participation that could compromise subject safety (e.g., hypersensitivity reactions, etc.);
- Subjects enrolled in the study despite not meeting eligibility criteria (inclusion/exclusion criteria violations).
- Prolongation of the QTcF interval on ECG recording (>500 ms or >60 ms compared to baseline measured on Days 1, 8, 15, and 22);
- Occurrence of a severe adverse event (AE) and/or serious adverse event (SAE) during study participation
- Missed collection of two or more consecutive blood samples for pharmacokinetic analysis or three or more samples within one pharmacokinetic study period;
- The volunteer is receiving or requires treatment that may affect the pharmacokinetic parameters of the study drug;
- Occurrence of vomiting/diarrhea within 8 hours after administration of the study drug;
- Positive urine test for narcotic substances and potent medicinal products;
- Positive breath alcohol test;
- Positive urine β-hCG test result in women;
- Emergence of any other reason during study participation that, in the Investigator's judgment, precludes the subject's continued compliance with protocol requirements.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: ACBD sequence
ACBD sequence, where: A - Ingavirin forte under fasting conditions; B - Ingavirin forte under fed conditions; C - Ingavirin under fasting conditions; D - Ingavirin under fed conditions.
|
Ingavirin forte containing 90 mg of imidazolylethanamide of pentanedioic acid and 20 mg of N,N'-bis-[2-(1,3-diazocyclopenta-2,4-dien-4-yl)ethyl] diamide of malonic acid (XC9)
Andre navne:
Ingavirin containing 90 mg of imidazolylethanamide of pentanedioic acid
Andre navne:
|
|
Eksperimentel: BADC sequence
BADC sequence, where: A - Ingavirin forte under fasting conditions; B - Ingavirin forte under fed conditions; C - Ingavirin under fasting conditions; D - Ingavirin under fed conditions.
|
Ingavirin forte containing 90 mg of imidazolylethanamide of pentanedioic acid and 20 mg of N,N'-bis-[2-(1,3-diazocyclopenta-2,4-dien-4-yl)ethyl] diamide of malonic acid (XC9)
Andre navne:
Ingavirin containing 90 mg of imidazolylethanamide of pentanedioic acid
Andre navne:
|
|
Eksperimentel: CDAB sequence
CDAB sequence, where: A - Ingavirin forte under fasting conditions; B - Ingavirin forte under fed conditions; C - Ingavirin under fasting conditions; D - Ingavirin under fed conditions.
|
Ingavirin forte containing 90 mg of imidazolylethanamide of pentanedioic acid and 20 mg of N,N'-bis-[2-(1,3-diazocyclopenta-2,4-dien-4-yl)ethyl] diamide of malonic acid (XC9)
Andre navne:
Ingavirin containing 90 mg of imidazolylethanamide of pentanedioic acid
Andre navne:
|
|
Eksperimentel: DBCA sequence
DBCA sequence, where: A - Ingavirin forte under fasting conditions; B - Ingavirin forte under fed conditions; C - Ingavirin under fasting conditions; D - Ingavirin under fed conditions.
|
Ingavirin forte containing 90 mg of imidazolylethanamide of pentanedioic acid and 20 mg of N,N'-bis-[2-(1,3-diazocyclopenta-2,4-dien-4-yl)ethyl] diamide of malonic acid (XC9)
Andre navne:
Ingavirin containing 90 mg of imidazolylethanamide of pentanedioic acid
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Pharmacokinetics - Cmax
Tidsramme: From 0 to 24 hours
|
Maximum plasma concentration (Cmax) of imidazolylethylamide of pentanedioic acid and N,N'-bis-[2-(1,3-diazocyclopent-2,4-dien-4-yl)ethyl] diamide of malonic acid.
The same analytes would be used for other pharmacokinetic measures listed below.
|
From 0 to 24 hours
|
|
Pharmacokinetics - tmax
Tidsramme: From 0 to 24 hours
|
Time to reach Cmax (tmax)
|
From 0 to 24 hours
|
|
Pharmacokinetics - AUC0-t
Tidsramme: From 0 to 24 hours
|
Area under the plasma concentration-time curve from time 0 to t (AUC0-t)
|
From 0 to 24 hours
|
|
Pharmacokinetics - AUC0-inf
Tidsramme: From 0 to 24 hours
|
Area under the plasma concentration-time curve from time 0 to infinity (AUC0-inf)
|
From 0 to 24 hours
|
|
Pharmacokinetics - AUCextr
Tidsramme: From 0 to 24 hours
|
Extrapolated AUC defined as (AUC0-inf - AUC0-t)/AUC0-inf
|
From 0 to 24 hours
|
|
Pharmacokinetics - t1/2
Tidsramme: From 0 to 24 hours
|
Elimination half-life (t1/2)
|
From 0 to 24 hours
|
|
Pharmacokinetics - kel
Tidsramme: From 0 to 24 hours
|
Elimination constant (kel)
|
From 0 to 24 hours
|
|
Pharmacokinetics - number of terminal timepoints
Tidsramme: From 0 to 24 hours
|
Number of points in the terminal logarithmic phase used to estimate the terminal elimination rate constant
|
From 0 to 24 hours
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Adverse event type
Tidsramme: From Screening to Day 29 ± 1
|
Adverse events will be assessed by complaints, results of physical examination, results of heart rate and blood pressure assessment, results of respiratory rate assessment, body temperature, laboratory monitoring (clinical blood count, biochemical blood count, urinalysis), electrocardiography; adverse events will be classified in accordance to MedDRA.
|
From Screening to Day 29 ± 1
|
|
Adverse event number
Tidsramme: From Screening to Day 29 ± 1
|
Number of adverse events registered during the study
|
From Screening to Day 29 ± 1
|
|
Adverse event severety
Tidsramme: From Screening to Day 29 ± 1
|
Severity of adverse events registered during the study, assessed using the Common Terminology Criteria for Adverse Events (CTCAE)
|
From Screening to Day 29 ± 1
|
|
Discontinuations due to adverse events related to the investigational product
Tidsramme: From Screening to Day 29 ± 1
|
Number of subjects who discontinued the study early due to adverse events (including serious adverse events) related to the investigational product
|
From Screening to Day 29 ± 1
|
|
Safety and Tolerability: volunteer complaints
Tidsramme: From Screening to Day 29 ± 1
|
Description of any health-related complaints received from volunteer
|
From Screening to Day 29 ± 1
|
|
Safety and Tolerability: physical examination results - cardiovascular system
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the cardiovascular system and associated symptoms on physical examination (normal condition or a description of abnormal conditions/cardiovascular symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: physical examination results - respiratory system
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the respiratory system and associated symptoms on physical examination (normal condition or a description of abnormal conditions/respiratory symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: physical examination results - digestive tract
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the digestive tract and associated symptoms on physical examination (normal condition or a description of abnormal conditions/digestive tract symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: physical examination results - endocrine system
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the endocrine system and associated symptoms on physical examination (normal condition or a description of abnormal conditions/endocrine symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: physical examination results - musculoskeletal system
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the musculoskeletal system and associated symptoms on physical examination (normal condition or a description of abnormal conditions/musculoskeletal symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: physical examination results - nervous system
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the nervous system and associated symptoms on physical examination (normal condition or a description of abnormal conditions/neurological symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: physical examination results - sensory systems
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the sensory systems and associated symptoms on physical examination (normal condition or a description of abnormal conditions/symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: physical examination results - skin/visible mucous membranes
Tidsramme: From Screening to Day 23
|
An assessment of the condition of the skin/visible mucous membranes and associated symptoms on physical examination (normal condition or a description of abnormal conditions/symptoms, if any)
|
From Screening to Day 23
|
|
Safety and Tolerability: vital signs - systolic blood pressure
Tidsramme: From Screening to Day 23
|
Systolic blood pressure (SBP, mmHg)
|
From Screening to Day 23
|
|
Safety and Tolerability: vital signs - diastolic blood pressure
Tidsramme: From Screening to Day 23
|
Diastolic blood pressure (DBP, mmHg)
|
From Screening to Day 23
|
|
Safety and Tolerability: vital signs - heart rate
Tidsramme: From Screening to Day 23
|
Heart rate (HR, bpm)
|
From Screening to Day 23
|
|
Safety and Tolerability: vital signs - body temperature (Celsius temperature scale)
Tidsramme: From Screening to Day 23
|
Body temperature (Celsius temperature scale)
|
From Screening to Day 23
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - heart rate
Tidsramme: From Screening to Day 23
|
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: heart rate (beats per minute)
|
From Screening to Day 23
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - PQ interval
Tidsramme: From Screening to Day 23
|
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: 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 Screening to Day 23
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - QRS complex
Tidsramme: From Screening to Day 23
|
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 Screening to Day 23
|
|
Safety and Tolerability: 12-lead electrocardiogram (ECG) - corrected QT interval
Tidsramme: From Screening to Day 23
|
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: corrected QT interval (distance from the beginning of the QRS complex to the end of the T wave; Fredericia correction)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - hemoglobin
Tidsramme: From Screening to Day 23
|
Hemoglobin (g/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - hematocrit
Tidsramme: From Screening to Day 23
|
Hematocrit (%)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - red blood cell count
Tidsramme: From Screening to Day 23
|
Red blood cell count (cells/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - platelet count
Tidsramme: From Screening to Day 23
|
Platelet count (cells/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - leukocyte count
Tidsramme: From Screening to Day 23
|
Leukocyte count (cells/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - erythrocyte sedimentation rate
Tidsramme: From Screening to Day 23
|
Erythrocyte sedimentation rate (mm/h)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - myelocytes
Tidsramme: From Screening to Day 23
|
Leukocyte formula (myelocytes, %)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - band neutrophils
Tidsramme: From Screening to Day 23
|
Leukocyte formula (band neutrophils, %)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - segmented neutrophils
Tidsramme: From Screening to Day 23
|
Leukocyte formula (segmented neutrophils, %)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - eosinophils
Tidsramme: From Screening to Day 23
|
Leukocyte formula (eosinophils, %)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - basophils
Tidsramme: From Screening to Day 23
|
Leukocyte formula (basophils, %)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - monocytes
Tidsramme: From Screening to Day 23
|
Leukocyte formula (monocytes, %)
|
From Screening to Day 23
|
|
Safety and Tolerability: clinical blood test - lymphocytes
Tidsramme: From Screening to Day 23
|
Leukocyte formula (lymphocytes, %)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - specific gravity
Tidsramme: From Screening to Day 23
|
Specific gravity of the urine
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - color
Tidsramme: From Screening to Day 23
|
Color of the urine
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - transparency
Tidsramme: From Screening to Day 23
|
Transparency of the urine
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - pH
Tidsramme: From Screening to Day 23
|
pH of the urine
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - protein
Tidsramme: From Screening to Day 23
|
Protein concentration (g/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - glucose
Tidsramme: From Screening to Day 23
|
Glucose concentration (mmol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - red blood cells
Tidsramme: From Screening to Day 23
|
Red blood cell content (number in sight)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - white blood cells
Tidsramme: From Screening to Day 23
|
White blood cell content (number in sight)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - epithelial cells
Tidsramme: From Screening to Day 23
|
Epithelial cell content (number in sight)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - casts
Tidsramme: From Screening to Day 23
|
Presence of casts (Yes/No)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - mucus
Tidsramme: From Screening to Day 23
|
Presence of mucus (Yes/No)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis - bacteria
Tidsramme: From Screening to Day 23
|
Presence of bacteria (Yes/No)
|
From Screening to Day 23
|
|
Safety and Tolerability: urinalysis (microscopy)
Tidsramme: From Screening to Day 23
|
Changes in urine sediment parameters (RBCs, WBCs, casts, crystals) as assessed by microscopy
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - glucose
Tidsramme: From Screening to Day 23
|
Glucose concentration (mmol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - cholesterol
Tidsramme: From Screening to Day 23
|
Total cholesterol concentration (mmol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - protein
Tidsramme: From Screening to Day 23
|
Total protein concentration (g/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - bilirubin
Tidsramme: From Screening to Day 23
|
Total bilirubin concentration (micromol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - creatinine
Tidsramme: From Screening to Day 23
|
Creatinine concentration (micromol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - alkaline phosphatase
Tidsramme: From Screening to Day 23
|
Alkaline phosphatase activity (U/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - alanine transaminase
Tidsramme: From Screening to Day 23
|
Alanine transaminase activity (U/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - aspartate transaminase
Tidsramme: From Screening to Day 23
|
Aspartate transaminase activity (U/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - potassium concentration
Tidsramme: From Screening to Day 23
|
Potassium (mmol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - sodium concentration
Tidsramme: From Screening to Day 23
|
Sodium concentration (mmol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - chloride concentration
Tidsramme: From Screening to Day 23
|
Chloride concentration (mmol/L)
|
From Screening to Day 23
|
|
Safety and Tolerability: blood chemistry - GFR
Tidsramme: From Screening to Day 23
|
Glomerular filtration rate, GFR (mL/min/1,73 м²)
|
From Screening to Day 23
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
11. juli 2025
Primær færdiggørelse (Anslået)
31. december 2027
Studieafslutning (Anslået)
31. december 2027
Datoer for studieregistrering
Først indsendt
12. maj 2026
Først indsendt, der opfyldte QC-kriterier
11. juni 2026
Først opslået (Faktiske)
12. juni 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
12. juni 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
11. juni 2026
Sidst verificeret
1. juni 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- IFR-01-02-2025
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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Kliniske forsøg med Influenza
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Gamaleya Research Institute of Epidemiology and...AfsluttetInfluenza A | Influenza A-virusinfektion | Influenza epidemi | Influenza H5N1Den Russiske Føderation
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NPO PetrovaxAfsluttetVaccine reaktion | Influenza | Influenza, menneske | Influenza A | Akut luftvejsinfektion | Influenza type B | Influenza | Influenza A H3N2 | Influenza A H1N1 | Influenza, menneske | Influenza epidemiDen Russiske Føderation
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Vanderbilt University Medical CenterHuman Vaccines ProjectAfsluttetVaccine reaktion | Influenza | Influenza, menneske | Influenza A | Influenza type B | Influenza A H3N2 | Influenza A H1N1Forenede Stater
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Institute of Medical Biology, Chinese Academy of...Guangxi Zhuang Autonomous Region Center for Disease Prevention and ControlIkke rekrutterer endnuInfluenza, menneske | Influenza virale infektioner | Influenza B | Influenza, menneskelig forebyggelse | Influenza aKina
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Institute of Medical Biology, Chinese Academy of...Guangxi Zhuang Autonomous Region Center for Disease Prevention and ControlAktiv, ikke rekrutterendeInfluenza, menneske | Influenza type B | Influenza virale infektioner | Influenza aKina
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SeqirusNovartis VaccinesAfsluttetInfluenza | Influenza, menneske | Influenza A-virus, H5N1-undertype | Influenza, menneske | Influenza, fugleAustralien, Tyskland, Italien
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ModernaTX, Inc.RekrutteringInfluenzaForenede Stater, Det Forenede Kongerige
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Novartis VaccinesAfsluttetInfluenza | Sæsonbestemt influenza | Menneskelig influenza | Influenza på grund af uspecificeret influenzavirusBelgien
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Novartis VaccinesNovartis Vaccines and Diagnostics (formerly Chiron Vaccines)AfsluttetInfluenza sygdom; InfluenzaForenede Stater
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National Institute of Allergy and Infectious Diseases...University of Minnesota; International Network for Strategic Initiatives...AfsluttetInfluenza A | Influenza BForenede Stater, Australien, Danmark, Det Forenede Kongerige
Kliniske forsøg med Ingavirin forte, capsules, 90 mg + 20 mg
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Valenta Pharm JSCRekruttering
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Valenta Pharm JSCAfsluttetCOVID-19Den Russiske Føderation
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Medicines for Malaria VentureGlaxoSmithKline; ICON plc; QIMR Berghofer Medical Research Institute; Southern... og andre samarbejdspartnereAfsluttetPatologiske processer | Infektioner | Systemisk inflammatorisk responssyndrom | Betændelse | Vektorbårne sygdomme | Parasitiske sygdomme | Protozoiske infektioner | Malaria | Parasitæmi | Malaria, Falciparum | Anti-infektionsmidler | AntimalariamidlerAustralien
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AlbionSprim Advanced Life SciencesUkendt
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Vanda PharmaceuticalsAfsluttetIkke-24-timers søvn-vågen lidelse
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Innovent Biologics (Suzhou) Co. Ltd.AfsluttetSkjoldbruskkirtlen øjensygdomKina
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Derma Techno PakistanAfsluttetKronisk spontan nældefeber (CSU)Pakistan
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Eisai Co., Ltd.Afsluttet
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Eisai Co., Ltd.Afsluttet
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E-nitiate Biopharmaceuticals (Hangzhou) Co., Ltd.Tilmelding efter invitationAtopisk dermatitis (AD)Kina