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- Register voor klinische proeven in de VS.
- Klinische proef NCT02256787
Safety, Tolerance, and Pharmacokinetics of Single Rising Oral Doses of BILB 1941 ZW Solution in Healthy Male Subjects, Followed With Bioavailability Comparison of BILB 1941 ZW Tablet and Solution Formulation Administered With or Without Food
2 oktober 2014 bijgewerkt door: Boehringer Ingelheim
Safety, Tolerance, and Pharmacokinetics of Single Oral Doses of 5 mg, 20 mg, 60 mg, 120 mg, 200 mg, 300 mg, 600 mg, 1000 mg, 1500 mg, 2000 mg, 2400 mg, and 3000 mg BILB 1941 ZW (PEG 400/TRIS Solution) in Healthy Male Subjects, in a Randomised Double Blind, Placebo Controlled Rising Dose Study, Followed With an Open-label Intra-subject Three-Way Crossover Bioavailability Comparison of 600 mg BILB 1941 ZW in a PEG 400/TRIS Solution and 600 mg BILB 1941 ZW Tablet and 600 mg BILB 1941 ZW Tablet Administered With Food
The objective of the current study was to investigate the safety, tolerability, and pharmacokinetics of BILB 1941 ZW following the administration of single rising doses from 5 mg to 300 mg.
In addition the bioavailability of the 60 mg dose given fasted and after a high-fat breakfast was to be be investigated
Studie Overzicht
Toestand
Voltooid
Conditie
Studietype
Ingrijpend
Inschrijving (Werkelijk)
56
Fase
- Fase 1
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
18 jaar tot 50 jaar (Volwassen)
Accepteert gezonde vrijwilligers
Ja
Geslachten die in aanmerking komen voor studie
Mannelijk
Beschrijving
Inclusion Criteria:
Healthy males according to the following criteria based upon a complete medical history, including the physical examination, vital signs (BP, PR), 12-lead ECG, clinical laboratory tests:
1.1 No finding deviating from normal and of clinical relevance
1.2 No evidence of a clinically relevant concomitant disease
- Age ≥18 and Age ≤50 years, BMI ≥18.5 and BMI ≤29.9 kg/m2 (Body Mass Index)
- Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice (GCP) and the local legislation
Exclusion Criteria:
- Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
- History or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic, hormonal disorders, including a clinical history of viral hepatitis, or serological evidence of active Hepatitis B or Hepatitis C infection
- History of orthostatic hypotension, fainting spells and blackouts
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- Chronic or relevant acute infections
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
- Intake of drugs with a long half-life (> 24 hours) within 1 month prior to administration
- Use of any drugs which might influence the results of the trial within 10 days prior to administration or during the trial
- Participation in another trial with an investigational drug within 1 month prior to administration or during the trial
- Smoker (> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on trial days
- Alcohol abuse (> 60 g/day)
- Drug abuse
- Blood donation of more than 100 mL within 1 month prior to administration or during the trial
- Excessive physical activities within 5 days prior to administration or during the trial
- Any laboratory value outside the clinically accepted reference range and of clinical relevance
- History of any familial bleeding disorder
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: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: BILB 1941 ZW - single rising dose
Single rising dose part
|
|
|
Placebo-vergelijker: Placebo
Single rising dose part
|
|
|
Experimenteel: BILB 1941 ZW - tablet - fasted
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
|
|
|
Experimenteel: BILB 1941 ZW - solution
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
|
|
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Experimenteel: BILB 1941 ZW - tablet - fed
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Number of subjects with abnormal findings in physical examination
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Number of subjects with abnormal changes in laboratory parameters
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Number of subjects with clinically significant changes in vital signs
Tijdsspanne: up to 48 hours following drug administration
|
Blood pressure, Pulse Rate
|
up to 48 hours following drug administration
|
|
Number of subjects with adverse events
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Number of subjects with clinically significant changes in 12-lead ECG (electrocardiogram)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Assessment of tolerability by investigator on a 4-point scale
Tijdsspanne: after 48 hours following drug administration
|
after 48 hours following drug administration
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
tmax (time from dosing to maximum concentration)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
AUC0-∞ (area under the concentration time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable data point)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
λz (terminal rate constant in plasma)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
t1/2 (terminal half-life of the analyte in plasma)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
MRT (Mean time of residence of drug molecules in the body after intravascular administration)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
Vz/F (Apparent volume of distribution during the terminal phase after extravascular administration)
Tijdsspanne: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Nuttige links
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
1 januari 2004
Primaire voltooiing (Werkelijk)
1 september 2004
Studieregistratiedata
Eerst ingediend
2 oktober 2014
Eerst ingediend dat voldeed aan de QC-criteria
2 oktober 2014
Eerst geplaatst (Schatting)
6 oktober 2014
Updates van studierecords
Laatste update geplaatst (Schatting)
6 oktober 2014
Laatste update ingediend die voldeed aan QC-criteria
2 oktober 2014
Laatst geverifieerd
1 oktober 2014
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- 1201.1
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