ASAR-CT 40/12.5 contains two active ingredients that lower blood pressure through complementary mechanisms.
The azilsartan medoxomil/chlorthalidone combination has been evaluated in randomized clinical trials.
Phase 3 study NCT01456169 evaluated azilsartan medoxomil 40 mg combined with chlorthalidone 12.5 mg or 25 mg in patients with hypertension who did not achieve target blood pressure with azilsartan monotherapy. The study enrolled 507 participants.
A separate randomized factorial study involving 1,714 patients evaluated different doses of azilsartan medoxomil and chlorthalidone. Fixed-dose combinations produced greater reductions in systolic blood pressure than either component used alone in the studied populations.
Another randomized study in patients whose hypertension remained uncontrolled after azilsartan monotherapy found that adding chlorthalidone enhanced blood pressure reduction. With the 40/12.5 mg combination, mean clinic systolic blood pressure decreased by 15.8 mmHg after 8 weeks, compared with 6.4 mmHg with azilsartan 40 mg alone.
These studies support the efficacy of the combination for blood pressure reduction. Individual treatment and dosage selection should be determined by a healthcare professional based on blood pressure response, kidney function, electrolyte levels, and other clinical factors.
ASAR-CT 40/12.5 is used for the treatment of arterial hypertension.
Azilsartan Medoxomil blocks the effects of angiotensin II, a hormone that promotes vasoconstriction and increased blood pressure. Chlorthalidone increases the renal excretion of sodium and water. Together, the two components lower blood pressure through complementary mechanisms.
Effective blood pressure control may reduce the long-term risk of cardiovascular complications, including stroke and target-organ damage.
The medication is taken orally once daily as prescribed by a healthcare professional. The tablet should be swallowed with water and may be taken with or without food. The appropriate dose is determined individually based on blood pressure response, kidney function, and other clinical factors. The dose should not be changed and treatment should not be discontinued without medical advice.
Patients should seek medical attention for severe dizziness, fainting, marked hypotension, reduced urine output, or other serious or persistent symptoms.









