The present study is planned to assess the safety, tolerability and pharmacokinetic profile of WCK 2349 in US subjects with selected ascending multiple doses of WCK 2349 and to compare the safety, tolerability and pharmacokinetic data with the data observed in similar studies conducted in India.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Enrollment
36
1 dose given orally twice daily at 12 hourly interval for five days.
Subjects will receive matching placebo
To evaluate the safety & tolerability of multiple doses of WCK 2349
By monitoring the adverse events reported
Time frame: 12 days
To evaluate the pharmacokinetics of multiple doses of WCK 2349
Measuring Cmax Maximum observed plasma concentration.
Time frame: 5 days
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