3 results
Primary:to assess the reduction of initial study drug Cmax after administration of 20 mg study drug 10% SRF using three modified formulations as compared to the current Phase 3 formulation in healthy volunteers.Secondary:to assess the safety and…
The purpose of the study is to confirm the skin test results in patients based on results of the control population of healthy volunteers never exposed to taspoglutide or any product with a similar mechanism of action.
The objectives of this study are:1) Assessing the user-friendliness of a self-sampling technique.2) Assessing the quality of the self-collected sample (volume and composition).3) To estimate the degree of agreement between viral loads in the self-…