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Baxdrostat/dapagliflozin

AstraZeneca · Phase 3 active Small molecule

Baxdrostat inhibits aldosterone synthase to reduce aldosterone production, while dapagliflozin inhibits SGLT2 to increase urinary glucose excretion and reduce sodium reabsorption.

Baxdrostat inhibits aldosterone synthase to reduce aldosterone production, while dapagliflozin inhibits SGLT2 to increase urinary glucose excretion and reduce sodium reabsorption. Used for Heart failure with reduced ejection fraction, Chronic kidney disease.

At a glance

Generic nameBaxdrostat/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, Nephrology
PhasePhase 3

Mechanism of action

This is a fixed-dose combination where baxdrostat blocks the final enzyme in aldosterone synthesis, reducing mineralocorticoid-mediated sodium retention and fibrosis, while dapagliflozin, an SGLT2 inhibitor, promotes glycosuria and natriuresis. Together, they target complementary pathways in heart failure and chronic kidney disease by reducing both aldosterone-driven and glucose-driven pathophysiology.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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