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Poster 2732004

Efficacy and safety of iclepertin (BI 425809) in patients with schizophrenia: CONNEX, a Phase III randomized controlled trial program

Corey Reuteman-Fowler - Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, USA
Zuzana Blahova - Boehringer Ingelheim RCV GmbH & Co. KG, Vienna, Austria
Satoru Ikezawa - International University of Health and Welfare, Mita Hospital, Mita, Minato-ku Tokyo, Japan
Stephen Marder - Semel Institute for Neuroscience at UCLA, David Geffen School of Medicine, Los Angeles, CA, USA
Peter Falkai - Clinic of Psychiatry and Psychotherapy, Ludwig Maximilians University Munich, Munich, Germany
John Krystal - Yale University School of Medicine, New Haven, CT, USA

Psych Congress Elevate 2024
Abstract: Rationale No effective pharmacological treatments are available for cognitive impairments in schizophrenia. Iclepertin (BI 425809), a glycine transporter-1 inhibitor, enhances N-methyl-D-aspartate receptor signaling by increasing synaptic levels of its co-agonist, glycine. In a Phase II proof-of-clinical-concept trial (NCT02832037) iclepertin was well tolerated and improved cognition in schizophrenia. The Phase III CONNEX program aims to confirm efficacy and safety of iclepertin in improving cognition/functioning across a large cohort of patients with schizophrenia. Methods The CONNEX program consists of 3 replicate randomized, double-blind, placebo-controlled parallel trials in patients with schizophrenia. 586 patients/trial will be recruited across 41 countries, and randomized 1:1 to receive daily iclepertin 10 mg or placebo over 26 weeks. Primary efficacy endpoint: change from baseline (CfB) in overall composite T-score of the Measurement and Treatment Research to Improve Cognition in Schizophrenia Consensus Cognitive Battery. Key secondary efficacy endpoints: CfB in total Schizophrenia Cognition Rating Scale score; CfB in the adjusted total time in the Virtual Reality Functional Capacity Assessment Tool. Long-term safety/tolerability data will be collected in an open-label safety extension study (CONNEX-X). Results The studies are currently recruiting (first participants enrolled Aug–Sept 2021), with completion expected in Q1 2025. Current study status, including screening failures and data collection experiences, are presented. Conclusions Most industry-sponsored studies testing compounds for cognitive deficits have failed to show proof-of-clinical-concept. If successful, the CONNEX program would provide evidence for iclepertin as the first efficacious medication addressing cognitive impairments in schizophrenia. Funding: These studies are funded by Boehringer Ingelheim (NCT04846868/1346-0011, NCT04846881/1346-0011, NCT04860830/1346-0013.)Short Description: Iclepertin (BI 425809) is a novel glycine transporter-1 inhibitor for the treatment of cognitive impairment associated with schizophrenia that has shown proof-of-clinical-concept and tolerability in a Phase II clinical trial. This abstract describes the Phase III CONNEX programme, which is currently recruiting approximately 1700 people with schizophrenia across 41 countries. CONNEX aims to confirm the efficacy, safety and tolerability of iclepertin in improving cognition and functioning in people with schizophrenia.Name of Sponsoring Organization(s): Boehringer Ingelheim.

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