- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02259881
Effect of BIBT 986 Followed by BIBT 986 Given as IV Infusion on Tissue Factor Triggered Coagulation in Healthy Male Volunteers
7. Oktober 2014 aktualisiert von: Boehringer Ingelheim
Investigation of the Effect of 0.9, 2.25 or 4.5 mg of BIBT 986 Over 1 Hour, Followed by 0.2, 0.5 or 1.0 mg/Hour of BIBT 986 for 7 Hours Given as IV Infusion on Tissue Factor Triggered Coagulation in a Randomised, Placebo Controlled, Dose Escalation Design in Healthy Male Volunteers
To compare with placebo the anticoagulant activity of three dosages of BIBT 986 on parameters of coagulation, platelet activation and inflammation in a model of tissue factor triggered activation of the coagulation system; to examine the safety of BIBT 986 in this setting
Studienübersicht
Status
Abgeschlossen
Bedingungen
Studientyp
Interventionell
Einschreibung (Tatsächlich)
64
Phase
- Phase 1
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre bis 40 Jahre (Erwachsene)
Akzeptiert gesunde Freiwillige
Ja
Studienberechtigte Geschlechter
Männlich
Beschreibung
Inclusion Criteria:
- Healthy male subjects as determined by the screening procedure
- Signed written informed consent form in accordance with good clinical practice (GCP) and local legislation was available
- Age ≥ 18 and ≤ 40 years
- Body mass index: BMI ≥ 18 and ≤ 29.9 kg/m2
- Normal findings in medical history and physical examination unless the investigator considered an abnormality to be clinically irrelevant
- Normal laboratory parameters unless the investigator considered an abnormality to be clinically irrelevant
Exclusion Criteria:
- Any finding in the medical examination (including blood pressure, pulse rate, ECG, and laboratory parameters) deviating from normal and of clinical relevance
- History of or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic, autoimmune, hormonal disorders, diseases of the central nervous system (such as epilepsy), or psychiatric disorders
- Symptoms of a clinically relevant illness in the 3 weeks before the first trial day
- History of orthostatic hypotension, fainting spells, and blackouts
- Chronic or relevant acute infections
- History of allergy / hypersensitivity (including drug allergy) which was deemed relevant to the trial as judged by the investigator
History of
- any bleeding disorder including prolonged or habitual bleeding
- any familial bleeding disorder
- other haematological disease
- cerebral bleeding (e.g. after a car accident)
- commotio cerebri
- Hereditary deficiency of protein C or S, or a mutation of factor V (Leiden), or any other known abnormality affecting coagulation, fibrinolysis, or platelet function
- Platelet count < 150000/μL
- Any ECG value outside of the reference range of clinical relevance (QRS interval > 110 ms or QTcB (QT interval Bazett correction) > 450 ms will be an obligatory exclusion criterion)
- Intake of drugs with a long half-life (> 24 hours) within 1 month prior to administration
- Use of any drugs that 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 2 months prior to administration or during trial
- Participation in an LPS trial within the last six weeks
- Smoker (> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on study days
- Concurrent or history of drug, alcohol, tobacco or coffee / tea / cola abuse
- Blood donation within 1 month prior to administration or during the trial
- Excessive physical activities within 5 days prior to administration or during the trial
- Seropositivity for hepatitis B surface antigen (HBs-Ag), hepatitis C virus (HCV), HIV 1, or HIV 2 antibodies
- Weight over 95 kg
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Doppelt
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Placebo-Komparator: Placebo
|
Endotoxin derived from E. coli bacteria, used for activation of coagulation
|
|
Experimental: Low dose of BIBT 986 CL
|
Endotoxin derived from E. coli bacteria, used for activation of coagulation
|
|
Experimental: Medium dose of BIBT 986 CL
|
Endotoxin derived from E. coli bacteria, used for activation of coagulation
|
|
Experimental: High dose of BIBT 986 CL
|
Endotoxin derived from E. coli bacteria, used for activation of coagulation
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in activated partial thromboplastin time (aPTT)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in international normalized ratio (INR)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in thrombin time (TT)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in ecarin clotting time (ECT)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in prothrombin fragment (F1+2)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in D-dimer
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in thrombin anti-thrombin complexes (TAT)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in protein C activity
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in antithrombin
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in thrombomodulin
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in tissue factor messenger RNA (mRNA)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in platelet count
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in plasmin antiplasmin complexes (PAP)
Zeitfenster: Pre-dose, up to day 14 after start of treatment
|
Pre-dose, up to day 14 after start of treatment
|
|
|
Change in soluble P-selectin
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in tumor necrosis factor alpha (TNF alpha)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in interleukin-6 (IL-6)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in primary haemostasis measured by closure times
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Number of subjects with clinically relevant changes in vital signs
Zeitfenster: up to 14 days after start of treatment
|
blood pressure, pulse rate, body temperature
|
up to 14 days after start of treatment
|
|
Number of subjects with clinically relevant changes in laboratory parameters
Zeitfenster: up to 14 days after start of treatment
|
up to 14 days after start of treatment
|
|
|
Number of subjects with adverse events
Zeitfenster: up to 14 days after start of treatment
|
up to 14 days after start of treatment
|
|
|
Number of subjects with clinically relevant changes in ECG
Zeitfenster: up to 14 days after start of treatment
|
up to 14 days after start of treatment
|
|
|
Change in thrombus precursor protein
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
|
Change in soluble E-selectin
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Area under the plasma concentration-time curve (AUC)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
Maximum concentration in plasma at the end of the infusion (Cgh)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
Apparent terminal half-life of BIBT 986 in plasma (t1/2)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
Mean residence time of BIBT 986 in the body after intravenous bolus administration (MRT)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
Volume of distribution of BIBT 986 in plasma at steady state (Vss)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
|
Apparent volume of distribution of BIBT 986 during the terminal phase after intravenous infusion (Vz)
Zeitfenster: up to 48 hours after start of treatment
|
up to 48 hours after start of treatment
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Nützliche Links
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. Dezember 2002
Primärer Abschluss (Tatsächlich)
1. Mai 2003
Studienanmeldedaten
Zuerst eingereicht
7. Oktober 2014
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
7. Oktober 2014
Zuerst gepostet (Schätzen)
9. Oktober 2014
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
9. Oktober 2014
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
7. Oktober 2014
Zuletzt verifiziert
1. Oktober 2014
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- 1192.11
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .