Dabigatran Etexilate
Drugdabigatran etexilate, orally, as 2 x 75-mg capsules (150 mg), single administration
NCT Number: NCT01379300
This is a study to investigate biomarkers after single oral doses of the anticoagulant agents dabigatran etexilate and rivaroxaban in healthy young male subjects and in healthy elderly subjects.
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Notify Me18 year–85 year
All sexes
Interventional
Phase 1
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
for non-hemophilia participants:
Panel A
Panel B
Both Panels
Exclusion criteria
for non-hemophilia participants:
Inclusion criteria
for hemophilia participants:
Exclusion criteria
for hemophilia participants:
dabigatran etexilate, orally, as 2 x 75-mg capsules (150 mg), single administration
rivaroxaban, orally, as 2 x 10-mg tablets (20 mg), single administration
Time frame: From up to 2 hours pre-dose to up to 24 hours post-dose
Time frame: From up to 2 hours pre-dose to up to 24 hours post-dose
Time frame: From up to 2 hours pre-dose to up to 24 hours post-dose
Time frame: From up to 2 hours pre-dose to up to 24 hours post-dose
Time frame: From up to 2 hours pre-dose to up to 24 hours post-dose
Merck Sharp & Dohme LLC
Industry
A Randomized Clinical Trial to Validate Novel Biomarker Approaches After Single Doses of Anticoagulants in Healthy Young Male Subjects and in Healthy Elderly Subjects
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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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