Drug intelligence / Profile preview

vadadustat + furosemide

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

Overview

**Vadadustat + furosemide** is an unapproved, non-branded experimental combination of two small molecule drugs: vadadustat, an oral hypoxia-inducible factor prolyl-hydroxylase (HIF-PH) inhibitor that stimulates endogenous erythropoietin for anemia of chronic kidney disease, and furosemide, a loop diuretic inhibiting sodium and chloride reabsorption in the kidney to promote diuresis. The combination has been studied to assess drug-drug interactions, particularly because vadadustat inhibits organic anion transporter 3 (OAT3), which may affect the renal elimination and activity of furosemide when co-administered. There is no unique fixed-dose pharmaceutical product; its clinical investigation centers on interaction potential in healthy subjects and patients with chronic kidney disease[1][2][3][4][6].

02

Targets

EGLN1 (Prolyl hydroxylase domain-containing protein 2)PHD3 (Prolyl hydroxylase domain-containing protein 3)SLC22A8 (Organic anion transporter 3)PHD1 (Prolyl hydroxylase domain-containing protein 1)EPAS1 (Hypoxia-inducible factor 2-alpha)HIF1A (Hypoxia-inducible factor 1-alpha)NKCC2 (Sodium-potassium-chloride cotransporter 2)

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