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Safety, Tolerability and Pharmacokinetics of Single Rising Oral Doses of BI 691751 in Healthy Asian Male Volunteers

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02057835
Recruitment Status : Completed
First Posted : February 7, 2014
Results First Posted : December 16, 2015
Last Update Posted : December 16, 2015
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim

Brief Summary:
BI 691751 is currently being developed to inhibit growth and prevent rupture of atherosclerotic plaques and to consequently reduce the risk of major cardiovascular events in patients with established atherosclerotic disease. 1334.5 is a Pan Asian Phase 1 study to investigate safety, tolerability and pharmacokinetics of BI 691751 in healthy Chinese and Japanese male volunteers.

Condition or disease Intervention/treatment Phase
Healthy Drug: Placebo to BI 691751 Drug: BI 691751 high dose Drug: BI 691751 middle dose Drug: BI 691751 low dose 1 Drug: BI 691751 low dose 2 Phase 1

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 64 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: Safety, Tolerability and Pharmacokinetics of Single Rising Oral Doses of BI 691751 in Healthy Asian Male Volunteers in a Randomised, Double-blind, Placebo-controlled Design.
Study Start Date : March 2014
Actual Primary Completion Date : May 2014
Actual Study Completion Date : May 2014

Arm Intervention/treatment
Experimental: BI 691751 low dose 1
BI 691751 low dose 1
Drug: Placebo to BI 691751
Placebo to BI 691751

Drug: BI 691751 low dose 1
BI 691751 low dose 1

Experimental: BI 691751 low dose 2
BI 691751 low dose 2
Drug: Placebo to BI 691751
Placebo to BI 691751

Drug: BI 691751 low dose 2
BI 691751 low dose 2

Experimental: BI 691751 middle dose
BI 691751 middle dose
Drug: BI 691751 middle dose
BI 691751 middle dose

Drug: Placebo to BI 691751
Placebo to BI 691751

Experimental: BI 691751 high dose
BI 691751 high dose
Drug: Placebo to BI 691751
Placebo to BI 691751

Drug: BI 691751 high dose
BI 691751 high dose




Primary Outcome Measures :
  1. Percentage of Participants With Drug Related Adverse Events [ Time Frame: From drug administration until 31 days after drug administration, 31 days ]
    Percentage of participants with drug related adverse events (AEs)


Secondary Outcome Measures :
  1. Maximum Measured Concentration of the Analyte (Cmax) [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Maximum measured concentration of the analyte in plasma/whole blood

  2. Maximum Measured Concentration of the Analyte (Cmax) - Overall [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Maximum measured concentration of the analyte in plasma/whole blood for all participants (Chinese and Japanese)

  3. Time From Dosing to the Maximum Measured Concentration of the Analyte (Tmax) [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Time from (last) dosing to the maximum measured concentration of the analyte in plasma/whole blood

  4. Time From Dosing to the Maximum Measured Concentration of the Analyte (Tmax) - Overall [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Time from (last) dosing to the maximum measured concentration of the analyte in plasma/whole blood for all participants (Chinese and Japanese)

  5. Area Under the Concentration-time Curve of the Analyte Over the Time Interval From 0 Extrapolated to Infinity (AUC0-infinity) [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Area under the concentration-time curve of the analyte in plasma/whole blood over the time interval from 0 extrapolated to infinity (AUC0-infinity)

  6. Area Under the Concentration-time Curve of the Analyte Over the Time Interval From 0 Extrapolated to Infinity (AUC0-infinity) - Overall [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Area under the concentration-time curve of the analyte in plasma/whole blood over the time interval from 0 extrapolated to infinity for all participants (Chinese and Japanese)

  7. Area Under the Concentration-time Curve of the Analyte Over the Time Interval From 0 to the Time of the Last Quantifiable Data Point (AUC0-tz) [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Area under the concentration-time curve of the analyte in plasma/whole blood over the time interval from 0 to the time of the last quantifiable data point (AUC0-tz)

  8. Area Under the Concentration-time Curve of the Analyte Over the Time Interval From 0 to the Time of the Last Quantifiable Data Point (AUC0-tz) - Overall [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Area under the concentration-time curve of the analyte in plasma/whole blood over the time interval from 0 to the time of the last quantifiable data point (AUC0-tz) for all participants (Chinese and Japanese)

  9. Terminal Half-life of the Analyte (T1/2) [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Terminal half-life (T1/2) of the analyte in plasma/whole blood

  10. Terminal Half-life of the Analyte (T1/2) - Overall [ Time Frame: 1 hour (h) before drug administration and 20minutes (min), 40min, 1h, 1h 30min, 2h, 2h 30min, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h, 48h, 60h, 72h, 96h, 120h, 144h, 192h, 240h, 288h and 336h after drug administration ]
    Terminal half-life (T1/2) of the analyte in plasma/whole blood for all participants (Chinese and Japanese)



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion criteria:

  1. Healthy males based upon a complete medical history, including a physical examination, vital signs (blood pressure, pulse rate), 12-lead ECG, and clinical laboratory tests
  2. Chinese ethnicity, Japanese ethnicity according to the following criteria:

    Chinese; born in China or ethnic Chinese born outside of China, and a descendent of 4 ethnic Chinese grandparents who were all born in China Japanese; born in Japan and holding Japanese passport, have lived outside of Japan <10 years, and have parents and grandparents who were all born in Japan

  3. Age within the range of 20 to 45 years
  4. Body mass index within the range of 18.5 and 25 kg/m2
  5. Signed and dated written informed consent prior to admission to the study in accordance with GCP and local legislation.

Exclusion criteria:

  1. Any finding in the medical examination (including BP, PR or ECG) deviating from normal and judged clinically relevant by the investigator. Pulse rate outside the range of 50-90 bpm or blood pressure outside the ranges of 90-140 for systolic and 50-90 mmHg for diastolic blood pressure if confirmed by repeat measurement.
  2. Any laboratory value outside the reference range that the investigator considers to be of clinical relevance
  3. Any evidence of a concomitant disease judged clinically relevant by the investigator
  4. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  5. Surgery of the gastrointestinal tract that could interfere with kinetics of the study drug
  6. Diseases of the central nervous system (such as epilepsy), central neurological disorders or psychiatric disorders
  7. History of relevant orthostatic hypotension, fainting spells, or blackouts
  8. Relevant chronic or acute infections
  9. History of relevant allergy/hypersensitivity (including allergy to the trial medication or its excipients)
  10. Intake of drugs with a long half-life (greater than 24 hours) within 30 days or less than 10 half-lives of the respective drug prior to study drug administration
  11. Use of drugs that might reasonably influence the results of the trial or that might prolong the QT/QTc interval within 14 days prior to study drug administration
  12. Participation in another trial with investigational drug administration within 60 days prior to administration of trial medication
  13. Smoker (more than 10 cigarettes or 3 cigars or 3 pipes/day)
  14. Inability to refrain from smoking on specified trial days
  15. Alcohol abuse (consumption of more than30 g/day)
  16. Drug abuse or positive drug screen
  17. Blood donation (more than 100 mL within 30 days prior to administration of trial medication or intended during the trial)
  18. Intention to perform excessive physical activities within one week prior to administration of trial medication or during the trial
  19. Inability to comply with dietary regimen of trial site
  20. A marked baseline prolongation of QT/QTc interval (such as repeated demonstration of a QTc interval greater than 450 ms) or any other relevant ECG finding
  21. A history of additional risk factors for Torsades de Pointes (such as heart failure, hypokalemia, or family history of Long QT Syndrome)
  22. Subject is assessed by the investigator as unsuitable for inclusion, for instance, because considered not able to understand and comply with study requirements, or has a condition that would not allow safe participation in the study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02057835


Locations
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Korea, Republic of
1334.5.82001 Boehringer Ingelheim Investigational Site
Seoul, Korea, Republic of
Sponsors and Collaborators
Boehringer Ingelheim
Investigators
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Study Chair: Boehringer Ingelheim Boehringer Ingelheim
Additional Information:
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Responsible Party: Boehringer Ingelheim
ClinicalTrials.gov Identifier: NCT02057835    
Other Study ID Numbers: 1334.5
First Posted: February 7, 2014    Key Record Dates
Results First Posted: December 16, 2015
Last Update Posted: December 16, 2015
Last Verified: November 2015