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To report the rationale for using PB‐201, a partial glucokinase activator (GKA), for a Phase 3 study (NCT05102149) assessing its efficacy and safety in a Chinese population and to describe the design of this GKA Phase 3 trial, the first to involve both an active control and a placebo control arm. The primary objective of this study was to monitor change in glycated haemoglobin levels with PB‐201 in treatment‐naive T2DM participants from baseline to 24 weeks in comparison with vildagliptin and placebo. This pivotal study will offer critical information regarding the efficacy and safety of PB‐201 in Chinese treatment‐naive T2DM participants that would help to establish robust evidence for the benefit‐risk evaluation of this drug.
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