- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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 ottobre 2014 aggiornato da: 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
Panoramica dello studio
Stato
Completato
Condizioni
Tipo di studio
Interventistico
Iscrizione (Effettivo)
56
Fase
- Fase 1
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
Da 18 anni a 50 anni (Adulto)
Accetta volontari sani
Sì
Sessi ammissibili allo studio
Maschio
Descrizione
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
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: BILB 1941 ZW - single rising dose
Single rising dose part
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Comparatore placebo: Placebo
Single rising dose part
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Sperimentale: BILB 1941 ZW - tablet - fasted
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
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Sperimentale: 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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Sperimentale: BILB 1941 ZW - tablet - fed
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Number of subjects with abnormal findings in physical examination
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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Number of subjects with abnormal changes in laboratory parameters
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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Number of subjects with clinically significant changes in vital signs
Lasso di tempo: up to 48 hours following drug administration
|
Blood pressure, Pulse Rate
|
up to 48 hours following drug administration
|
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Number of subjects with adverse events
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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Number of subjects with clinically significant changes in 12-lead ECG (electrocardiogram)
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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Assessment of tolerability by investigator on a 4-point scale
Lasso di tempo: after 48 hours following drug administration
|
after 48 hours following drug administration
|
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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tmax (time from dosing to maximum concentration)
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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AUC0-∞ (area under the concentration time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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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)
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
λz (terminal rate constant in plasma)
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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t1/2 (terminal half-life of the analyte in plasma)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
Collegamenti utili
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio
1 gennaio 2004
Completamento primario (Effettivo)
1 settembre 2004
Date di iscrizione allo studio
Primo inviato
2 ottobre 2014
Primo inviato che soddisfa i criteri di controllo qualità
2 ottobre 2014
Primo Inserito (Stima)
6 ottobre 2014
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
6 ottobre 2014
Ultimo aggiornamento inviato che soddisfa i criteri QC
2 ottobre 2014
Ultimo verificato
1 ottobre 2014
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- 1201.1
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .