Head-to-head evidence

Baxdrostat vs Lorundrostat

Same mechanism, same race: design-graded trial evidence for both assets, with the grading rationale shown. Grades describe the quality of the evidence, never the merits of either security.

Hypertension

Shared mechanism: Aldosterone synthase (CYP11B2) · full Hypertension pipeline

Baxdrostat · Baxfendy

Marketed by AstraZeneca

Approved in Hypertensionsmall molecule
Reliable signal

NCT06034743 · Phase 3 · completed

The trial randomized 794 participants to baxdrostat or matching placebo and used quadruple masking of participants, care providers, investigators, and outcome assessors. Both prespecified primary blood-pressure endpoints were met at Week 12: the reduction in seated systolic blood pressure was greater with 2 mg and 1 mg baxdrostat than with placebo, with p<0.0001 for each comparison.

Next expected readout: December 2026 · NCT07222917 (registry estimate)

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Lorundrostat

Developed by Mineralys Therapeutics

Phase 3 in Hypertensionsmall molecule
Reliable signal

NCT05432167 · Phase 2 · completed

In this 195-participant randomized, double-blind, placebo-controlled trial, the primary clinical endpoint was met: pooled CIN-107 reduced seated systolic blood pressure by 15.22 mmHg versus 7.15 mmHg with placebo, a between-group difference of 8.08 mmHg (p=0.003). The trial had a substantial sample size and the primary comparison was statistically significant in the favorable direction.

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Chronic Kidney Disease

Shared mechanism: Aldosterone synthase (CYP11B2) · full Chronic Kidney Disease pipeline

Baxdrostat · Baxfendy

Marketed by AstraZeneca

Phase 3 in Chronic Kidney Diseasesmall molecule
not yet graded

No graded featured trial for this indication yet; the grade above reflects that absence, not a judgment.

Next expected readout: December 2026 · NCT07222917 (registry estimate)

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Lorundrostat

Developed by Mineralys Therapeutics

Phase 2 in Chronic Kidney Diseasesmall molecule
Reliable signal

NCT05432167 · Phase 2 · completed

In this 195-participant randomized, double-blind, placebo-controlled trial, the primary clinical endpoint was met: pooled CIN-107 reduced seated systolic blood pressure by 15.22 mmHg versus 7.15 mmHg with placebo, a between-group difference of 8.08 mmHg (p=0.003). The trial had a substantial sample size and the primary comparison was statistically significant in the favorable direction.

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The full competitive landscape for each asset (every same-race competitor with aligned evidence, sortable) is on the asset pages: Baxdrostat's landscape · Lorundrostat's landscape