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Translational Psychiatry· 2026Q1

A randomized, controlled experimental medicine study of the novel Kv7 channel opener azetukalner in individuals with major depressive disorder and anhedonia

Rachel Fremont, Philipp T. Neukam, Usha S. Govindarajulu, Jessica L. Ables et al.

Short summary

Azetukalner (20 mg/day) did not significantly alter ventral striatum (VS) activity during reward anticipation in individuals with major depressive disorder (MDD) and anhedonia compared to placebo over 8 weeks (n=60).

AI-generated from the title and abstract; the full text is not read.

Key points

  • Azetukalner did not significantly change VS activity during reward anticipation in MDD patients with anhedonia.
  • No statistically significant improvement was observed in depression (MADRS) or anhedonia (SHAPS) scores compared to placebo.
  • Numerical benefits favoring azetukalner were noted in secondary and exploratory endpoints.
  • Azetukalner was well-tolerated, with low and similar discontinuation rates due to adverse events across groups.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Major Depressive Disorder (MDD) is a common and debilitating disease. Kv7 potassium channels are relevant to reward processing and represent a novel target for depression and anhedonia. Azetukalner is a positive allosteric modulator of Kv7 channels. This phase II, randomized, double-blind, placebo-controlled trial assessed changes in brain reward function, clinical outcomes, and safety following treatment with azetukalner or placebo in individuals with MDD and anhedonia. The study included 60 participants with MDD and anhedonia in a current major depressive episode. Participants were randomized 1:1 to receive azetukalner (20 mg orally once daily with food) or placebo for 8 weeks. The primary endpoint was change in bilateral ventral striatum (VS) activity assessed by functional MRI (fMRI) during a reward task from baseline to week 8. Secondary endpoints included changes in depression severity and anhedonia measured by the Montgomery-Åsberg Depression Rating Scale (MADRS) and Snaith-Hamilton Pleasure Scale (SHAPS). Of 60 participants, 29 were randomized to azetukalner and 31 to placebo. There was no significant difference in VS response to reward anticipation between groups. Compared to placebo, azetukalner was associated with numerical benefit on the MADRS and SHAPS that did not reach statistical significance. Most exploratory endpoints numerically favored azetukalner over placebo. Discontinuation rates due to adverse events were low and did not differ across groups. Despite not meeting the primary neuroimaging endpoint, secondary and exploratory outcomes suggested potential improvement in depressive symptoms and anhedonia. Trial Registration: Clinicaltrials.gov ID NCT04827901.

The authors' abstract, as published at the source. Translational Psychiatry, 2026 · DOI ↗

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Field: Pharmacology (Medicine)

PharmacologyMedicine