ClinConnect ClinConnect Logo
Search / Trial NCT02264119

Influence of Pantoprazole on the Pharmacokinetics of Fradafiban After Multiple Oral Doses of Lefradafiban in Healthy Subjects

Launched by BOEHRINGER INGELHEIM · Oct 13, 2014

Trial Information

Current as of June 01, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • Healthy male subjects as determined by results of screening
  • Signed written informed consent in accordance with good clinical practice (GCP) and local legislation
  • Age ≥ 18 and ≤ 60 years, planned stratification: age \< 40 years (4 subjects) and ≥ 40 years (8 subjects)
  • Broca ≥ - 20 % and ≤ + 20 %
  • Exclusion Criteria:
  • Use of any drugs which might influence the results of the trial within 10 days prior to administration or during the trial
  • Intake of drugs with a long half-life (\> 24 hours) within 1 month prior to administration
  • Participation in another trial with an investigational drug within 2 months prior to administration or during the trial
  • Drug abuse
  • Alcohol abuse (\> 60 g/day)
  • Smoker (\> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on study days
  • Excessive physical activities within 5 days prior to administration or during the trial
  • Blood donation within 1 month prior to administration or during the trial
  • History or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological, hormonal disorders
  • Chronic or relevant acute infections
  • Diseases of the central nervous system (such as epilepsy) or psychiatric disorders
  • History of
  • Allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
  • Any bleeding disorder including prolonged or habitual bleeding
  • Other hematologic disease
  • Cerebral bleeding (e.g. after a car accident)
  • Recent surgical procedures
  • Thrombocytes \< 150000/µ
  • Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
  • Any laboratory value outside the clinically accepted reference range
  • Other disease or abnormality of clinical relevance

About Boehringer Ingelheim

Boehringer Ingelheim is a global, research-driven pharmaceutical company dedicated to improving health and quality of life through innovative therapies. Established in 1885 and headquartered in Ingelheim, Germany, the company focuses on the development of prescription medicines in key therapeutic areas, including respiratory diseases, cardiovascular health, oncology, and immunology. Boehringer Ingelheim is committed to advancing medical science through rigorous clinical trials and collaborative research, striving to bring novel treatments to patients while upholding the highest standards of safety and efficacy. With a strong emphasis on sustainability and corporate responsibility, the company aims to make a meaningful impact on global health challenges.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials