Pharmacodynamics, Safety and Pharmacokinetics After Oral Administration of BIBR 1048 MS in Healthy Volunteers
Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
The objective of this study was to assess safety, pharmacokinetics and the effect of BIBR 953
ZW on coagulation parameters of BIBR 953 ZW after oral single doses of the prodrug, BIBR 1048
MS, in healthy male subjects. This was the first administration of this substance to humans.