Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Oral Doses of BI 14332 CL Powder in Healthy Male Subjects
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Oral Doses (0.5 mg to 200 mg) of BI 14332 CL as Powder in the Bottle Reconstituted With 0.1% Tartaric Acid Administered to Healthy Male Subjects. A Randomised and Placebo-controlled Trial, Double Blinded Within Dose Groups
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Faktiske)
Tilmelding
Fase
Fase
- Fase 1
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Healthy males were included based on a complete medical history, including the physical examination, vital signs (BP, HR), 12-lead ECG, and clinical laboratory tests
- Age ≥18 and Age ≤50 years
- Body Mass Index (BMI) ≥18.5 and BMI ≤29.9 kg/m2
- Signed and dated written informed consent prior to admission to the study in accordance with GCP and the local legislation
Exclusion Criteria:
- Any finding of the medical examination (including BP, HR and ECG) deviating from normal and of clinical relevance
- Any evidence of a clinically relevant concomitant disease
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of relevant orthostatic hypotension, fainting spells or blackouts
- Chronic or relevant acute infections
- History of relevant allergy/hypersensitivity (including allergy to drug or its excipients)
- Intake of drugs with a long half-life (>24 hours) within at least one month or less than 10 half-lives of the respective drug prior to administration or during the trial
- Use of drugs which reasonably influenced the results of the trial based on the knowledge at the time of protocol preparation within 10 days prior to administration or during the trial
- Participation in another trial with an investigational drug within two months prior to administration or during the trial
- Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
- Inability to refrain from smoking on trial days
- Alcohol abuse (more than 60 g/day)
- Drug abuse
- Blood donation (more than 100 mL within four weeks prior to administration or during the trial)
- Excessive physical activities (within one week prior to administration or during the trial)
- Any laboratory value outside the reference range and of clinical relevance
- Inability to comply with the dietary regimen of the study centre
- Any ECG value outside the reference range and of clinical relevance including, but not limited to QRS interval >120 ms or a marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval >450 ms or QT >500 ms)
- A history of additional risk factors for Torsades des Pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
- The use of concomitant medications that prolong the QT/QTc interval
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Placebo komparator: Placebo
|
|
|
Eksperimentel: BI 14332 CL
single rising dose
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Number of patients with adverse events
Tidsramme: up to day 16
|
up to day 16
|
|
Number of patients with clinically significant findings in vital signs (blood pressure, heart rate)
Tidsramme: up to day 16
|
up to day 16
|
|
Number of patients with clinically significant findings ECG
Tidsramme: up to day 16
|
up to day 16
|
|
Number of patients with clinically significant findings laboratory tests
Tidsramme: up to day 16
|
up to day 16
|
|
Assessment of global tolerability by investigator on a 4-point scale
Tidsramme: within 9 to 16 days after drug administration
|
within 9 to 16 days after drug administration
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
AUC0-∞ (areal under koncentration-tid-kurven for analytten i plasma over tidsintervallet fra 0 ekstrapoleret til uendeligt)
Tidsramme: op til 192 timer efter lægemiddeladministration
|
op til 192 timer efter lægemiddeladministration
|
|
AUC0-tz (areal under koncentration-tid-kurven for analytten i plasma over tidsintervallet fra 0 til tidspunktet for det sidste kvantificerbare datapunkt)
Tidsramme: op til 192 timer efter lægemiddeladministration
|
op til 192 timer efter lægemiddeladministration
|
|
λz (terminalhastighedskonstant i plasma)
Tidsramme: op til 192 timer efter lægemiddeladministration
|
op til 192 timer efter lægemiddeladministration
|
|
t1/2 (terminal halveringstid af analytten i plasma)
Tidsramme: op til 192 timer efter lægemiddeladministration
|
op til 192 timer efter lægemiddeladministration
|
|
MRTpo (gennemsnitlig opholdstid for analytten i kroppen efter oral administration)
Tidsramme: op til 192 timer efter lægemiddeladministration
|
op til 192 timer efter lægemiddeladministration
|
|
Vz/F (tilsyneladende distributionsvolumen under den terminale fase λz efter en ekstravaskulær dosis)
Tidsramme: op til 192 timer efter lægemiddeladministration
|
op til 192 timer efter lægemiddeladministration
|
|
Cmax (maximum concentration of the analyte in plasma)
Tidsramme: up to 192 hours after drug administration
|
up to 192 hours after drug administration
|
|
tmax (time from dosing to maximum concentration)
Tidsramme: up to 192 hours after drug administration
|
up to 192 hours after drug administration
|
|
%AUCtz-∞ (the percentage of the AUC0-∞ that is obtained by extrapolation)
Tidsramme: up to 192 hours after drug administration
|
up to 192 hours after drug administration
|
|
CL/F (total clearance of the analyte in the plasma after extravascular administration)
Tidsramme: up to 192 hours after drug administration
|
up to 192 hours after drug administration
|
|
Aet1-t2 (amount of analyte that is eliminated in urine from the time point t1 to time point t2)
Tidsramme: up to 120 hours after drug administration
|
up to 120 hours after drug administration
|
|
fet1-t2 (fraction of analyte eliminated in urine from time point t1 to time point t2)
Tidsramme: up to 120 hours after drug administration
|
up to 120 hours after drug administration
|
|
CLR,t1-t2 (renal clearance of the analyte from the time point t1 until the time point t2)
Tidsramme: up to 120 hours after drug administration
|
up to 120 hours after drug administration
|
|
Change in Dipeptidyl peptidase IV (DDP-IV) activity
Tidsramme: up to 192 hours after drug administration
|
up to 192 hours after drug administration
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Publikationer og nyttige links
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart
Studiestart
Primær færdiggørelse (Faktiske)
Primær færdiggørelse
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 1233.1
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