Drug intelligence / Profile preview

dapagliflozin + rosuvastatin placebo

Development stage
Unknown
Lead developer
CMG Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Dapagliflozin + rosuvastatin placebo is a clinical trial comparator arm used to evaluate the efficacy and safety of the fixed-dose combination CMG190303 (dapagliflozin/rosuvastatin). Developed by CMG Pharmaceutical Co. Ltd., this intervention consists of active dapagliflozin (10 mg) and an inactive placebo for rosuvastatin. It is utilized in Phase 3 trials (such as NCT06772168) targeting patients with comorbid type 2 diabetes mellitus and dyslipidemia. Dapagliflozin is a small molecule inhibitor of the sodium-glucose cotransporter-2 (SGLT2), which reduces blood glucose levels by inhibiting renal glucose reabsorption and promoting its excretion in the urine. The rosuvastatin placebo serves to maintain the double-blind nature of the study while isolating the effects of dapagliflozin alone.

Other names
Comparator 1: Dapagliflozin/Rosuvastatin placebodapagliflozin 10mg + rosuvastatin placebo
02

Targets

SLC5A1 (Sodium Glucose Cotransporter 1)SGLT2 (Sodium-glucose cotransporter protein subunit 2)

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