The purpose of this study is to determine the safety and tolerability of CoFactor in healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Parexel International - Baltimore CPRU
Baltimore, Maryland, United States
Pharmacokinetic profile of CoFactor formulations in healthy adult subjects.
To measure the 5,10 methylenetetrahydrofolic acid levels after CoFactor and leucovorin administration
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.