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

7. oktober 2014 opdateret af: 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

Studieoversigt

Status

Afsluttet

Betingelser

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

39

Fase

  • Fase 1

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

21 år til 50 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Han

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

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo
Eksperimentel: Epinastine nasal
single rising doses

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
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
Foranstaltningsbeskrivelse
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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Hjælpsomme links

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. august 2001

Primær færdiggørelse (Faktiske)

1. september 2001

Datoer for studieregistrering

Først indsendt

7. oktober 2014

Først indsendt, der opfyldte QC-kriterier

7. oktober 2014

Først opslået (Skøn)

9. oktober 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

9. oktober 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

7. oktober 2014

Sidst verificeret

1. oktober 2014

Mere information

Begreber relateret til denne undersøgelse

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Placebo

Abonner