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OpenTrials
Completed

NCT Number: NCT02260037

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

Safety, tolerability and pharmacokinetics

Completed

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Key information

Conditions

Age range

21 year–50 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Epinastine nasal

Drug

Placebo

Drug

Primary outcomes

  1. Number of patients with clinically relevant findings in vital signs

    Time frame: up to 8 days after drug administration

    blood pressure, pulse rate

  2. Number of patients with clinically relevant findings in 12-lead ECG

    Time frame: up to 8 days after drug administration

  3. Number of patients with adverse events

    Time frame: up to 8 days after drug administration

  4. Number of patients with clinically relevant findings in laboratory parameters

    Time frame: up to 8 days after drug administration

  5. Changes in rhinoscopy assessment

    Time frame: up to 8 days after drug administration

Secondary outcomes

  1. Maximum measured concentration in plasma (Cmax)

    Time frame: up to 48 hours after drug administration

  2. Time from dosing to the maximum concentration in plasma (tmax)

    Time frame: up to 48 hours drug administration

  3. Area under the concentration-time curve in plasma (AUC)

    Time frame: up to 48 hours after drug administration

  4. Terminal rate constant of in plasma (λz)

    Time frame: up to 48 hours after drug administration

  5. Apparent terminal half-life in plasma (t1/2)

    Time frame: up to 48 hours after drug administration

  6. Total mean residence time in the body (MRTtot)

    Time frame: up to 48 hours after drug administration

  7. Total clearance in plasma after extravascular administration (CL/F)

    Time frame: up to 48 hours after drug administration

  8. Apparent volume of distribution during the terminal phase (Vz/F)

    Time frame: up to 48 hours after drug administration

  9. Amount excreted into urine (Ae)

    Time frame: up to 48 hours after drug administration

  10. Renal clearance (CLR)

    Time frame: up to 48 hours after drug administration

  11. Assessment of dose-proportionality of epinastine nasal

    Time frame: up to 48 hours after drug administration

    based on AUC and Cmax

Sponsors and collaborators

Lead sponsor

Boehringer Ingelheim

Industry

Registry information

Official study title

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))

Important dates

Study start
2001
Primary completion
2001
First posted
Oct 9, 2014
Registry last updated
Oct 9, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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