The time course of blood drug concentration of irbesartan tablets after a single oral administration of fasting oral administration to healthy subjects was studied, the corresponding pharmacokinetic parameters were estimated, and the bioequivalence evaluation was performed using the product before the prescription change (Ambrovi) as the standard reference preparation.
The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3
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