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Study Reference No. - 20-244

Study Type Demographic Gender Age Location Compensation
Investigational Oral Medication Healthy volunteers Males and Females 18 - 55 years old Saint Petersburg FL $1,300.00
Study Details

Study Objective

The purpose of this study is to see if an investigational [new/not available on the market and not yet approved by the U.S. Food and Drug Administration (FDA)] capsule is bioequivalent (to see if the active test study drug is absorbed into the body at the same rate and amount as an already approved drug)] to a currently marketed capsule, as well as to monitor the safety of the study subjects.

Study Duration

Approx. 11 Days

Study Schedule

General Screening

N/A

Medical Screening

Feb 10th - 11th, 15th - 19th

Study Visit(s)

Group 1, Period 1: Mar, Mon 8th - Wed 10th

Ambulatory visit 1: Night of Wed 10th

Ambulatory visit 2: Morning of Thu 11th

Group 1, Period 2: Mar, 15th - Wed 17th

Ambulatory visit 1: Night of Wed 17th

Ambulatory visit 2: Morning of Thu 18th

Group 2, Period 1: Mar, Wed 11th - Sat 11th

Ambulatory visit 1: Night of Sat 11th

Ambulatory visit 2: Morning of Sun 12th

Group 2 Period 2: Mar, Wed 18th - Sat 20th

Ambulatory visit 1: Night of Sat 20th

Ambulatory visit 2: Morning of Sun 21th

Other Notes

Study Requires overnight stays