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CONNEX-3: A Study to Test Whether Iclepertin Improves Learning and Memory in People With Schizophrenia

Phase 3
Completed
Conditions
Schizophrenia
Interventions
Drug: Placebo
Registration Number
NCT04860830
Lead Sponsor
Boehringer Ingelheim
Brief Summary

This study is open to adults with schizophrenia. Schizophrenia can affect the way a person thinks, their memory and their mental functioning. Examples include struggling to remember things, or to read a book or pay attention to a movie. Some people have difficulty calculating the right change or planning a trip so that they arrive on time. The purpose of this study is to find out whether a medicine called iclepertin improves learning and memory in people with schizophrenia.

Participants are put into two groups randomly, which means by chance. One group takes iclepertin tablets and the other group takes placebo tablets. Placebo tablets look like iclepertin tablets but do not contain any medicine. Participants take a tablet once a day for 26 weeks. In addition, all participants take their normal medication for schizophrenia.

During this time, doctors regularly test learning and memory of the participants by use of questionnaires, interviews, and computer tests. The results of the mental ability tests are compared between the groups.

Participants are in the study for about 8 months and visit the study site about 14 times. During this time, doctors regularly check participants' health and take note of any unwanted effects.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
609
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Iclepertin treatment groupBI 425809-
Placebo groupPlacebo-
Primary Outcome Measures
NameTimeMethod
Change from baseline in overall composite T-score of the Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) consensus cognitive battery (MCCB)After 26 weeks of treatment

MCCB comprises 10 tests, which assess 7 cognitive domains, including speed of processing, attention vigilance, working memory, verbal learning, visual learning, reasoning and problem solving, and social cognition

Secondary Outcome Measures
NameTimeMethod
Change from baseline to Week 26 in the adjusted total time in the Virtual Reality Functional Capacity Assessment Tool (VRFCAT)Up to week 26
Change from baseline to Week 26 in the T-score of the number of correct responses on Tower of LondonUp to week 26
Change from baseline in the Schizophrenia Cognition Rating Scale (SCoRS) interviewer total scoreAfter 26 weeks of treatment

SCoRS is a 20-item interview-based assessment of cognitive deficits and the degree to which they affect day-to-day functioning. Each item is rated on a 4-point scale. Higher ratings reflect a greater degree of impairment.

Change from screening visit 1a to Week 24 in Patient Reported Experience of Cognitive Impairment in Schizophrenia (PRECIS) total scoreUp to week 24

PRECIS is a patient reported outcome (PRO) for recording patients' subjective experience of Cognitive Impairment Associated with Schizophrenia (CIAS). The questionnaire contains 28 items covering 6 domains: Memory (6 items), communication (4 items), self-control (3 items), executive function (4 items), attention (6 items), and sharp thinking (3 items). Two additional items assess the overall degree of bother associated with all domains. Questions are answered via a 5-category Likert scale, with higher scores corresponding to worse patient experience. The Total Score is derived by calculating the simple average score of the first 26 items.

Trial Locations

Locations (110)

Sunwise Clinical Research-Walnut Creek-70166

🇺🇸

Walnut Creek, California, United States

Synexus Clinical Research-Atlanta-67262

🇺🇸

Atlanta, Georgia, United States

Hassman Research Institute-Berlin-60540

🇺🇸

Berlin, New Jersey, United States

LinQ Research, LLC-Richmond-70076

🇺🇸

Richmond, Texas, United States

Advanced Research Center, Inc.

🇺🇸

Anaheim, California, United States

ProScience Research Group

🇺🇸

Culver City, California, United States

University of California Los Angeles

🇺🇸

Los Angeles, California, United States

CNRI - Los Angeles

🇺🇸

Pico Rivera, California, United States

Stanford University Medical Center

🇺🇸

Stanford, California, United States

Advanced Medical Research Group Inc

🇺🇸

Hollywood, Florida, United States

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Sunwise Clinical Research-Walnut Creek-70166
🇺🇸Walnut Creek, California, United States

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