Clinical trial to evaluate the tolerability and pharmacokinetics of a new ultra low molecular weight heparin (RO-14) administered subcutaneously increasing single-doses to healthy male volunteers
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
12
Hospital Santa Creu i Sant Pau
Barcelona, Spain
Main objective : To evaluate safety and tolerability of increasing single-doses to healthy male volunteers
Time frame: safety parameters
Secondary objectives : To evaluate pharmacokinetics profiles of each of single-doses.
Time frame: anti-Xa activity
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