- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02171806
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of BI 1744 CL in Healthy Male and Female Volunteers
20. juni 2014 oppdatert av: Boehringer Ingelheim
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses (2.5 μg, 10 μg, and 30 μg) of BI 1744 CL for 14 Days in Healthy Male and Female Volunteers (Doubleblind, Randomised, Placebo Controlled [at Each Dose Level] Study)
To investigate safety, tolerability, pharmacokinetics and pharmacodynamics of BI 1744 CL
Studieoversikt
Studietype
Intervensjonell
Registrering (Faktiske)
47
Fase
- Fase 1
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
21 år til 50 år (Voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Healthy male or female based upon a complete medical history, including the physical examination, regarding vital signs (blood pressure (BP), pulse rate (PR)), 12-lead ECG measurement, and clinical laboratory tests. There is no finding deviating from normal and of clinical relevance. There is no evidence of a clinically relevant concomitant disease.
- Age ≥21 and ≤50 years
- BMI ≥18.5 and <30 kg/m2 (Body Mass Index)
- Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice and the local legislation
Exclusion Criteria:
- Any finding of the medical examination (including BP, PR, and ECG measurements) deviating from normal and of clinical relevance
- 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 the drug or its excipients) as judged clinically relevant by the investigator
- Intake of drugs with a long half-life (>24 hours) within at least 1 month or less than 10 half-lives of the respective drug prior to randomisation
- Use of drugs which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation within 10 days prior to randomisation
- Participation in another trial with an investigational drug within 2 months prior to randomisation
- Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
- Inability to refrain from smoking on trial days as judged by the investigator
- Alcohol abuse (more than 60 g alcohol a day)
- Drug abuse
- Blood donation (more than 100 mL blood within 4 weeks prior to randomisation or during the trial)
- Excessive physical activities within 1 week prior to randomisation or during the trial
- Any laboratory value outside the reference range that is of clinical relevance
- Inability to comply with dietary regimen of the study centre
The following exclusion criteria are specific for this study due to the known class side effect profile of ß2-mimetics:
- Asthma or history of pulmonary hyperreactivity
- Hyperthyrosis
- Allergic rhinitis in need of treatment
- Clinically relevant cardiac arrhythmia
- Paroxysmal tachycardia (>100 beats per minute).
For female subjects:
- Pregnancy
- Positive pregnancy test
- No adequate contraception e.g. oral contraception, sterilisation, IUD (intrauterine device). Females who are not surgically sterile will be asked to additionally use barrier contraception methods (e.g. condoms) prior to administration of study medication, during the study and at least 2 months after release from the study.
- Inability to maintain this adequate contraception during the whole study period
- Lactation period
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Placebo komparator: Placebo
|
|
|
Eksperimentell: BI 1744 CL multiple rising doses
|
|
|
Eksperimentell: BI 1744 CL medium dose, females
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Number of patients with clinically significant changes in physical examination
Tidsramme: Baseline, day 32 (end-of-study examination)
|
Baseline, day 32 (end-of-study examination)
|
|
Number of patients with clinically significant changes in vital signs
Tidsramme: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with clinically significant changes in 12-lead ECG (Electrocardiogram)
Tidsramme: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with abnormal changes in laboratory tests
Tidsramme: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Changes in airway resistance (Raw) measured by body plethysmography
Tidsramme: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Changes in tremormetry parameters
Tidsramme: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with adverse events
Tidsramme: Up to day 32
|
Up to day 32
|
|
Assessment of tolerability by the investigator on a 4-point scale
Tidsramme: Day 32 (end-of-study examination)
|
Day 32 (end-of-study examination)
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
tmax (time from dosing to maximum concentration)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
AUC (area under the concentration-time curve of the analyte in plasma at different time points)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 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 384 hours after drug administration
|
Up to 384 hours after drug administration
|
|
fet1-t2 (fraction of analyte eliminated in urine from time point t1 to time point t2)
Tidsramme: Up to 384 hours after drug administration
|
Up to 384 hours after drug administration
|
|
%AUCtz-∞ (the percentage of the AUC 0-∞ that is obtained by extrapolation)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
λz (terminal rate constant of the analyte in plasma)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
t½ (terminal half-life of the analyte in plasma)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
MRTih (mean residence time of the analyte in the body after inhalation)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
CL/F (apparent clearance of the analyte in the plasma after extravascular administration)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Vz/F (apparent volume of distribution of the analyte during the terminal phase λz following an extravascular dose)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
CLR,t1-t2 (renal clearance of the analyte in plasma from the time point t1 until the time point t2)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
RA,Cmax,14 based on Cmax (Accumulation ratio of the analyte in plasma after multiple dose administration over a uniform dosing interval τ)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
RA,AUC,14 based on AUC0-τ
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Cmin,ss (minimum measured concentration of the analyte in plasma at steady state over a uniform dosing interval τ)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Cpre,ss (predose concentration of the analyte in plasma at steady state immediately before administration of the next dose)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Linearity Index (LI)
Tidsramme: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Hjelpsomme linker
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. januar 2006
Primær fullføring (Faktiske)
1. september 2006
Datoer for studieregistrering
Først innsendt
20. juni 2014
Først innsendt som oppfylte QC-kriteriene
20. juni 2014
Først lagt ut (Anslag)
24. juni 2014
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
24. juni 2014
Siste oppdatering sendt inn som oppfylte QC-kriteriene
20. juni 2014
Sist bekreftet
1. juni 2014
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 1222.2
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .