Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Dose Tolerance Study in Healthy Male Volunteers After Intranasal Application of Epinastine Nasal

7. oktober 2014 oppdatert av: Boehringer Ingelheim

A Double-blind, Randomised, Placebo-controlled Single Increasing Dose Tolerance Study in Healthy Male Volunteers After Intranasal Application of Epinastine Nasal (Dosage: 0.035 mg (0.025 % Solution) - 0.42 mg (0.3 % Solution))

Safety, tolerability and pharmacokinetics

Studieoversikt

Status

Fullført

Forhold

Studietype

Intervensjonell

Registrering (Faktiske)

39

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

Ja

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

Inclusion Criteria:

  • All participants in the study should be healthy, range from 21 to 50 years of age and be within ± 20 % of their normal weight (Broca -Index)
  • Subsequently each subject will have his medical history taken and will receive a complete medical examination (incl. blood pressure and pulse rate measurements) as well as a 12-lead ECG. Haematological, hepatic and renal function tests will be carried out in the laboratory (Bioscientia Ingelheim, Germany). The subjects will fast for 12 hours before collection of specimens for all laboratory evaluations. The above mentioned examinations will be performed within 14 days before the first administration of the test substance
  • In accordance with good clinical practice (GCP) and the local legislation all volunteers will have given their written informed consent prior to admission to the study

Exclusion Criteria:

  • Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  • Surgery of the gastro-intestinal tract (except appendectomy)
  • Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  • History of orthostatic hypotension, fainting spells or blackouts
  • 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 at least one month or less than ten half-lives of the respective drug before enrolment in the study
  • Use of any drugs which might influence the results of the trial (≤ one week prior to administration or during the trial)
  • Participation in another trial with an investigational drug (≤ 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 (> 60 g/day)
  • Drug abuse
  • Blood donation (≥ 100 mL within four weeks prior to administration or during the trial)
  • Excessive physical activities (within the last week before the study)
  • Any laboratory value outside the reference range of clinical relevance

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: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: Placebo
Eksperimentell: Epinastine nasal
single rising doses

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of patients with clinically relevant findings in vital signs
Tidsramme: up to 8 days after drug administration
blood pressure, pulse rate
up to 8 days after drug administration
Number of patients with clinically relevant findings in 12-lead ECG
Tidsramme: up to 8 days after drug administration
up to 8 days after drug administration
Number of patients with adverse events
Tidsramme: up to 8 days after drug administration
up to 8 days after drug administration
Number of patients with clinically relevant findings in laboratory parameters
Tidsramme: up to 8 days after drug administration
up to 8 days after drug administration
Changes in rhinoscopy assessment
Tidsramme: up to 8 days after drug administration
up to 8 days after drug administration

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Maximum measured concentration in plasma (Cmax)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Time from dosing to the maximum concentration in plasma (tmax)
Tidsramme: up to 48 hours drug administration
up to 48 hours drug administration
Area under the concentration-time curve in plasma (AUC)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Terminal rate constant of in plasma (λz)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Apparent terminal half-life in plasma (t1/2)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Total mean residence time in the body (MRTtot)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Total clearance in plasma after extravascular administration (CL/F)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Apparent volume of distribution during the terminal phase (Vz/F)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Amount excreted into urine (Ae)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Renal clearance (CLR)
Tidsramme: up to 48 hours after drug administration
up to 48 hours after drug administration
Assessment of dose-proportionality of epinastine nasal
Tidsramme: up to 48 hours after drug administration
based on AUC and Cmax
up to 48 hours after drug administration

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

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. august 2001

Primær fullføring (Faktiske)

1. september 2001

Datoer for studieregistrering

Først innsendt

7. oktober 2014

Først innsendt som oppfylte QC-kriteriene

7. oktober 2014

Først lagt ut (Anslag)

9. oktober 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

9. oktober 2014

Siste oppdatering sendt inn som oppfylte QC-kriteriene

7. oktober 2014

Sist bekreftet

1. oktober 2014

Mer informasjon

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. .

Kliniske studier på Sunn

Kliniske studier på Placebo

3
Abonnere