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Baxdrostat and dapagliflozin

AstraZeneca · Phase 3 active Small molecule

Baxdrostat inhibits aldosterone synthase to reduce aldosterone production, while dapagliflozin inhibits SGLT2 to increase urinary glucose excretion, together addressing both hypertension/heart failure and glycemic control.

Baxdrostat inhibits aldosterone synthase to reduce aldosterone production, while dapagliflozin inhibits SGLT2 to increase urinary glucose excretion, together addressing both hypertension/heart failure and glycemic control. Used for Heart failure with reduced ejection fraction, Hypertension with cardiometabolic disease.

At a glance

Generic nameBaxdrostat and dapagliflozin
Also known asBaxdrostat CIN-107
SponsorAstraZeneca
Drug classAldosterone synthase inhibitor + SGLT2 inhibitor combination
TargetCYP11B2 (aldosterone synthase) and SGLT2 (sodium-glucose cotransporter 2)
ModalitySmall molecule
Therapeutic areaCardiovascular, Diabetes
PhasePhase 3

Mechanism of action

Baxdrostat is a non-steroidal aldosterone synthase inhibitor that decreases aldosterone levels, reducing sodium retention and blood pressure while improving cardiac function. Dapagliflozin is an SGLT2 inhibitor that promotes urinary glucose excretion and has cardioprotective and renoprotective effects. The combination targets complementary pathways in cardiometabolic disease.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results