Drug intelligence / Profile preview

CIN-107 + metformin

Development stage
Phase 1
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

**CIN-107 + metformin** is a combination of two pharmaceutical agents: CIN-107 (baxdrostat), a highly potent and selective oral small molecule inhibitor of human aldosterone synthase (CYP11B2), and metformin, a well-established antihyperglycemic agent of the biguanide class. CIN-107 reduces aldosterone synthesis, resulting in decreased sodium retention and blood pressure, without affecting cortisol levels[1][3][5]. Metformin acts by decreasing hepatic glucose production, suppressing gastrointestinal absorption of glucose, and improving peripheral insulin sensitivity[2][5]. Combination therapy is investigated mainly for patients with hypertension and/or type 2 diabetes, with pharmacokinetic studies confirming no impact of CIN-107 on systemic exposure to metformin and no clinically significant pharmacodynamic interactions[1][4][5]. The combination is particularly relevant in subjects with hypertension and comorbid diabetes due to potential additive/synergistic effects on blood pressure and metabolic control.

Other names
CIN-107 + metforminbaxdrostat + metformin
02

Targets

AMPK (Adenosine monophosphate–activated protein kinase)CYP11B2 (Cytochrome P450 11B2)

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