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📊 Resource Allocation by Research Phase:
📚 Data Analysis
🧪 Experimental Design
🔬 Clinical Trials
💊 Treatment Development
The pharmacokinetics of 50 mg BIBR 1048 administered as two newly developed...
Status
Completed
Location
Multiple Locations
Start Date
2001-04
Trial ID
NCT02170805
To assess the steady state pharmacokinetic profile of BIBR 953 ZW after adm...
Status
Completed
Location
Multiple Locations
Start Date
2002-11
Trial ID
NCT02173730
Treatments Being Tested
Study to investigate the relative bioavailability of BIBR 953 ZW after admi...
Status
Completed
Location
Multiple Locations
Start Date
2003-08
Trial ID
NCT02170597
Treatments Being Tested
Study to investigate and compare safety, pharmacokinetics and pharmacodynam...
Status
Completed
Location
Multiple Locations
Start Date
2004-12
Trial ID
NCT02170909
Treatments Being Tested
To assess the extent of absorption of 12.5, 50 and 200 mg of BIBR 1048 MS w...
Status
Completed
Location
Multiple Locations
Start Date
2001-02
Trial ID
NCT02170792
Treatments Being Tested
Vitamin K antagonists were hampered by several disadvantages, such as the n...
Status
Completed
Location
CHU Besancon
Start Date
2014-11-13
Trial ID
NCT02103101
Two substudies to assess (1) the tolerability of BIBR 953 ZW intravenous in...
Status
Completed
Location
Multiple Locations
Start Date
2001-01
Trial ID
NCT02170584
Treatments Being Tested
To investigate safety, pharmacokinetics and pharmacodynamics of BIBR 1048 M...
Status
Completed
Location
Multiple Locations
Start Date
2005-04
Trial ID
NCT02171000
Treatments Being Tested
The objective of this study was to assess safety, pharmacokinetics and the ...
Status
Completed
Location
Multiple Locations
Start Date
1998-11
Trial ID
NCT02170116
To assess safety, pharmacokinetics and the effect of BIBR 1048 MS on coagul...
Status
Completed
Location
Multiple Locations
Start Date
1999-05
Trial ID
NCT02170831