Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of BEA 2180 BR in Healthy Male Subjects

October 13, 2014 updated by: Boehringer Ingelheim

Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of Single Rising Inhaled BEA 2180 BR Doses (2.5 μg to 1600 μg Cation Administered With the Respimat®) in Healthy Male Subjects, Alone and Followed by Methacholine Challenge. A Randomised, Double-blind Within Dose Group, Placebo-controlled Study, With a 36 μg Tiotropium Bromide Single Dose Sub-study (Open, Two-fold Crossover).

Main study: To investigate safety, tolerability, pharmacodynamics (PD) and pharmacokinetics (PK) of BEA 2180 BR Sub-study; To investigate whether treatment with 36 μg tiotropium bromide is able to protect of methacholine-induced bronchoconstriction compared to baseline (methacholine challenge at screening).

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
101

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 1

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

30 years to 55 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Healthy male volunteers based upon a complete medical history, including the physical examination, vital signs (BP, PR), 12-lead ECG, clinical laboratory test
  • No finding deviating from normal and of clinical relevance
  • No evidence of a clinically relevant concomitant disease
  • Age ≥ 30 and Age ≤ 55 years
  • Body Mass Index (BMI) ≥ 18.5 and BMI < 30 kg/m2
  • Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice and the local legislation

Exclusion Criteria:

  • 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 allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator (or his deputy)
  • 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 might reasonably influence 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
  • 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 of clinical relevance

Exclusion criteria specific for this study:

  • Bronchial hyperreactivity as demonstrated by a 45% change of SGaw at or below a cumulative methacholine concentration of 10 mg/mL = 1%
  • Asthma or bronchial hyperreactivity
  • Allergic rhinitis (hay fever)
  • Glaucoma
  • Urinary tract obstruction
  • Epilepsy
  • History of cardiovascular disease
  • History of peptic ulcer disease
  • History of thyroid disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Placebo Comparator: Placebo
Drug: Placebo
Device: Respimat® A 4
Drug: Methacholine Chloride
methacholine challenge test
Experimental: BEA 2180 BR
single rising doses
Drug: BEA 2180 BR
Device: Respimat® A 4
Drug: Methacholine Chloride
methacholine challenge test
Experimental: Sub-Study
Drug: Methacholine Chloride
methacholine challenge test
Drug: Spiriva
Other Names:
  • tiotropium bromide

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Number of subjects with clinically significant changes in vital signs
Time Frame: up to 14 days after last drug administration
blood pressure, pulse rate, respiratory rate, oral body temperature
up to 14 days after last drug administration
Number of subjects with clinically significant changes in laboratory parameters
Time Frame: up to 14 days after last drug administration
up to 14 days after last drug administration
Changes from baseline in airway resistance (Raw)
Time Frame: up to 120 hours after drug administration
assessed by body plethysmography
up to 120 hours after drug administration
Changes from baseline in specific airway conductance (sGaw)
Time Frame: up to 120 hours after drug administration
assessed by body plethysmography
up to 120 hours after drug administration
Number of subjects with clinically significant findings in 12-lead ECG (electrocardiogram)
Time Frame: up to 14 days after last drug administration
up to 14 days after last drug administration
Number of subjects with adverse events
Time Frame: up to 14 days after last drug administration
up to 14 days after last drug administration
Assessment of tolerability by investigator on a 5-point scale
Time Frame: within 14 days after last drug administration
within 14 days after last drug administration

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Changes from baseline in salivary secretion
Time Frame: up to 24 hours after drug administration
up to 24 hours after drug administration
Changes from baseline in pupil diameter of each eye
Time Frame: up to 4 hours after drug administration
pupillometry
up to 4 hours after drug administration
Maximum measured concentration of the analyte in plasma (Cmax)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration
Measured concentration of the analyte in plasma (C) for several time points
Time Frame: up to 24 hours after drug administration
up to 24 hours after drug administration
Time from dosing to the maximum concentration of the analyte in plasma (tmax)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration
Amount of parent drug that is eliminated in urine (Ae)
Time Frame: up to 312 hours after drug administration
up to 312 hours after drug administration
Fraction of administered drug excreted unchanged in urine (fe)
Time Frame: up to 312 hours after drug administration
up to 312 hours after drug administration
Area under the concentration-time curve of the analyte in plasma (AUC)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration
Renal clearance of the analyte (CLR)
Time Frame: up to 312 hours after drug administration
up to 312 hours after drug administration
Terminal rate constant of the analyte in plasma (λZ)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration
Terminal half-life of the analyte in plasma (t1/2)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration
Mean residence time of the analyte in the body after inhaled administration (MRTinh)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration
Apparent clearance of the analyte in plasma following extravascular administration (CL/F)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration
Apparent volume of distribution during the terminal phase λz following an extravascular dose (VZ/F)
Time Frame: up to 240 hours after drug administration
up to 240 hours after drug administration

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Boehringer Ingelheim

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
August 1, 2003

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
June 1, 2004

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
October 13, 2014

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
October 13, 2014

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
October 15, 2014

Study Record Updates

Last Update Posted (Estimate)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
October 15, 2014

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
October 13, 2014

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
October 1, 2014

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • 1205.1
  • 1205.9001 (Other Identifier: Boehringer Ingelheim)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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