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Completed

NCT Number: NCT02171689

Metabolism and Pharmacokinetics of [14C]- BIBW 2992 MA2 in Healthy Male Volunteers

The aim of the study was to investigate the metabolism and pharmacokinetics of BIBW 2992 MA2 after a single oral dose of [14C]-radiolabelled BIBW 2992 MA2 in healthy male volunteers. Metabolites in human plasma and excretions were measured, the structures of the metabolites analysed and compared with metabolites in animals. In addition, the mass-balance of excretion, the protein binding of [14C]-radioactivity, the plasma concentrations of BIBW 2992 MA2, and the [14C]-radioactivity in blood cells, plasma, urine and faeces were measured. The safety and tolerability of BIBW 2992 were also investigated.

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Key information

Conditions

Age range

35 year–60 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

  • Healthy male subjects as determined by results of screening
  • Signed written informed consent in accordance with Good Clinical Practice and local legislation
  • Age ≥35 and ≤60 years
  • Body Mass Index ≥18.5 kg/m2 and ≤29.9 kg/m2

Exclusion criteria

  • Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
  • History or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic, hormonal disorders
  • History of any major surgery within the last four weeks before participation in this study or any bone fracture within the last two months
  • History of orthostatic hypotension, fainting spells and blackouts
  • Diseases of the central nervous system (such as epilepsy) or psychiatric disorders
  • 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 1 month prior to administration
  • Planned use of any drugs which might influence the results of the trial within 10 days prior to administration or during the trial
  • Participation in another trial with an investigational drug within 2 months prior to administration or during trial
  • Smoker (> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on study days
  • Alcohol abuse (> 60 g/day)
  • Drug abuse
  • Blood donation within 1 month prior to administration or during the trial
  • Excessive physical activities within 5 days prior to administration or during the trial
  • Any laboratory value outside the reference range, unless considered to lack clinical reference
  • Male subjects must agree to minimize the risk of female partners becoming pregnant from the dosing day until 3 months after the completion of the study. Acceptable methods of contraception for male volunteers include a vasectomy no less than 3 months prior to dosing, barrier contraception or a medically accepted contraceptive method. For female partners of male volunteers, acceptable methods of contraception include intra-uterine device, tubal ligation, hormonal contraceptive since at least two months and diaphragm with spermicide

Treatment and study plan

[14C]- BIBW 2992 MA2

Drug

Primary outcomes

  1. [14C]-radioactivity in plasma and whole blood (CBlood cells/Cplasma ratio of [14C]-radioactivity)

    Time frame: up to 96 hours after drug administration

  2. [14C]-radioactivity in urine and faeces (excretion mass balance)

    Time frame: up to 120 hours after drug administration

  3. Measurement of the plasma protein binding of total [14C]-radioactivity

    Time frame: up to 96 hours after drug administration

  4. Concentrations of the analyte in plasma, urine, and faeces

    Time frame: up to 96 hours after drug administration

  5. Cmax (maximum observed concentration of the analyte in plasma)

    Time frame: up to 96 hours after drug administration

  6. tmax (time from dosing to peak concentration (Cmax))

    Time frame: up to 96 hours after drug administration

  7. t1/2 (terminal half-life of the analyte in plasma)

    Time frame: up to 96 hours after drug administration

  8. λz (terminal rate constant of the analyte in plasma)

    Time frame: up to 96 hours after drug administration

  9. AUC (area under the concentration-time curve of the analyte in plasma) for different time points

    Time frame: up to 96 hours after drug administration

  10. MRTpo (mean residence time of the analyte molecules in the body after oral administration)

    Time frame: up to 96 hours after drug administration

  11. CL/F (total clearance of the analyte in plasma following extravascular administration)

    Time frame: up to 96 hours after drug administration

  12. Vz/F (apparent volume of distribution during the terminal phase following extravascular administration)

    Time frame: up to 96 hours after drug administration

  13. fe0-tz (fraction of analyte eliminated in urine or faeces from 0 to the limit of the last quantifiable data point)

    Time frame: up to 120 hours after drug administration

  14. Aet0-tz (amount of analyte eliminated in urine or faeces from 0 the limit of the last quantifiable data point)

    Time frame: up to 120 hours after drug administration

  15. Plasma concentration time profiles of the analyte

    Time frame: up to 96 hours after drug administration

  16. Plasma concentration-time profiles of total radioactivity in whole blood and plasma

    Time frame: up to 96 hours after drug administration

  17. [14C]-metabolic profile and identification of metabolites in urine, faeces, blood cells and plasma

    Time frame: up to 120 hours after drug administration

Secondary outcomes

  1. Number of patients with clinically relevant changes in vital signs (Pulse rate (PR), systolic and diastolic blood pressure (BP))

    Time frame: Baseline, day 2, within 14 days after study drug administration

  2. Number of patients with clinically relevant changes in ECG (electrocardiogram)

    Time frame: Baseline, day 2, within 14 days after study drug administration

  3. Number of patients with clinically relevant changes in laboratory parameters

    Time frame: Baseline, day 2, within 14 days after study drug administration

  4. Number of patients with adverse events

    Time frame: up to 27 days

  5. Assessment of tolerability on a 4-point scale

    Time frame: within 14 days after study drug administration

Sponsors and collaborators

Lead sponsor

Boehringer Ingelheim

Industry

Registry information

Official study title

Metabolism and Pharmacokinetics of [14C]- BIBW 2992 MA2 After Administration of Single Doses of 15 mg [14C]- BIBW 2992 MA2 Oral Solution in Healthy Male Volunteers

Important dates

Study start
2006
Primary completion
2006
First posted
Jun 24, 2014
Registry last updated
Jun 24, 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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