Contemporary Clinical Trials Communications (Mar 2020)

Add-on spironolactone as antagonist of the NRG1-ERBB4 signaling pathway for the treatment of schizophrenia: Study design and methodology of a multicenter randomized, placebo-controlled trial

  • Alkomiet Hasan,
  • Astrid Roeh,
  • Stefan Leucht,
  • Berthold Langguth,
  • Maximilian Hansbauer,
  • Tatiana Oviedo-Salcedo,
  • Sophie K. Kirchner,
  • Irina Papazova,
  • Lisa Löhrs,
  • Elias Wagner,
  • Isabel Maurus,
  • Wolfgang Strube,
  • Moritz J. Rossner,
  • Michael C. Wehr,
  • Ingrid Bauer,
  • Stephan Heres,
  • Claudia Leucht,
  • Peter M. Kreuzer,
  • Stephanie Zimmermann,
  • Thomas Schneider-Axmann,
  • Thomas Görlitz,
  • Susanne Karch,
  • Silvia Egert-Schwender,
  • Beate Schossow,
  • Philipp Rothe,
  • Peter Falkai

Journal volume & issue
Vol. 17

Abstract

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Background: Preclinical studies recently showed that the mineralocorticoid antagonist spironolactone acts also as an antagonist of the NRG1-ERBB4 signaling pathway and improves schizophrenia-like behaviour in Nrg1 transgenic mouse model. As this signaling pathway is critically linked to the pathophysiology of schizophrenia, especially in the context of working-memory dysfunction, spironolactone may be a novel treatment option for patients with schizophrenia targeting cognitive impairments. Aims: To evaluate whether spironolactone added to an ongoing antipsychotic treatment improves cognitive functioning in schizophrenia. Methods: The add-on spironolactone for the treatment of schizophrenia trial (SPIRO-TREAT) is a multicenter randomized, placebo-controlled trial with three arms (spironolactone 100 mg, spironolactone 200 mg and placebo). Schizophrenia patients are treated for three weeks and then followed-up for additional nine weeks. As primary outcome, we investigate changes in working memory before and at the end of the intervention phase. We will randomize 90 patients. Eighty-one patients are intended to reach the primary endpoint measure at the end of the three-week intervention period. Secondary endpoints include other measures of cognition, psychopathology, safety measures and biological measures. Conclusions: SPIRO-TREAT is the first study evaluating the efficacy of the mineralocorticoid receptor antagonist spironolactone to improve cognitive impairments in schizophrenia patients targeting the NRG1-ERBB4 signaling pathway. With SPIRO-TREAT, we intend to investigate a novel treatment option for cognitive impairments in schizophrenia that goes beyond the established concepts of interfering with dopaminergic neurotransmission as key pathway in schizophrenia treatment. Clinical trial registration: International Clinical Trials Registry Platform: http://apps.who.int/trialsearch/Trial2.aspx?TrialID=EUCTR2014-001968-35-DE Keywords: Schizophrenia, Cognitive impairment, Spironolactone, NRG1-ERBB4, Drug repositioning, Drug repurposing