Monument Therapeutics MT1988 First Patient Dosed
Cambridge Cognition Holdings plc announced that its 20% owned associate, Monument Therapeutics, has dosed the first patient in a clinical trial for MT1988, a potential treatment for individuals at clinical high risk for psychosis. This randomized, placebo-controlled study will enroll 150 participants over an eight-week period to evaluate MT1988's efficacy in improving cognitive symptoms, utilizing both clinical and cognitive biomarkers, with Cambridge Cognition's digital assessment technologies supporting the trial's foundational biomarker strategy.
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Cambridge Cognition Investment, Monument Therapeutics, Announces First Patient Dosed in Clinical Trial of MT1988 in Patients at Clinical High Risk for Psychosis
Cambridge UK, March 11, 2026 - Cambridge Cognition (AIM: COG), the neuroscience technology company whose digital cognitive assessments drive scientific discovery, accelerate drug development and improve patient care, reports that Monument Therapeutics Limited ("Monument"), in which the Group has a 20% shareholding, has announced the dosing of the first patient in its clinical trial with MT1988, to treat patients at clinical high risk (CHR) for psychosis.
The study is being conducted in collaboration with the Foundation for the National Institutes of Health (FNIH) as part of the Accelerating Medicines Partnership® Schizophrenia (AMP® SCZ) program. This trial marks a major step forward in developing treatment options for people at risk of schizophrenia.
The randomised, placebo-controlled, proof-of-principle study will enrol 150 CHR participants who will receive one of two dose levels of MT1988 or placebo over an eight-week treatment period. The trial will evaluate the potential of MT1988 to improve cognitive symptoms in CHR individuals, incorporating a range of clinical and cognitive biomarkers. This approach is designed to assess not only therapeutic effects but also the potential of these biomarkers to predict and monitor treatment response.
Cambridge Cognition's proprietary digital cognitive assessment technologies supported the early development of MT1988 and were instrumental in establishing the foundational biomarker strategy for Monument.
Sheryl Caswell, Chief Development Officer of Monument Therapeutics said "Dosing our first patient marks a pivotal moment for Monument Therapeutics and for people at risk of developing psychosis, because, despite the significant impact of this early stage of illness, there are currently no approved pharmacological treatments for the CHR population."
Rob Baker, Chief Executive Officer - Cambridge Cognition said, "We congratulate our colleagues at Monument for achieving this milestone in MT1988's development. Treatment of the first patient represents a significant value inflection point for Monument. We believe using both biological biomarkers and Cambridge Cognition's digital assessments of cognitive function to assess MT1988 will provide insights into the underlying biology and also capture observable changes in cognitive function."
- require minimal specialist administration
- deliver objective results in real time or shortly after completion
- reduce administrator bias
- support longitudinal monitoring of cognitive function
- CANTAB One™ - a brief assessment of overall cognitive function
- CANTAB Insight™ - a three-task battery providing deeper insight across five cognitive sub-domains
Monument Therapeutics is a neuroscience-focused drug development company headquartered in Manchester, UK. It applies a unique and novel drug development strategy, leveraging digital assessments of cognition to select patients suitable for treatment with the innovative drugs that it is developing.
For more information, please visit www.monumenttx.com.
About the Foundation for the National Institutes of Health:
The Foundation for the National Institutes of Health (FNIH) builds public-private partnerships that connect leading biomedical scientists at the National Institutes of Health (NIH) with their counterparts in life sciences companies, academia, patient organizations, foundations, and regulatory agencies (including the U.S. Food and Drug Administration and European Medicines Agency). Through team science, the FNIH solves complex health challenges and accelerates breakthroughs for patients, regardless of who they are or what health threats they face. The FNIH contributes to the development of new therapies, diagnostics, and potential cures; advances global health; and helps train the next generations of scientists. Established by Congress in 1990 to support the mission of the NIH, the FNIH is a not-for-profit 501(c)(3) charitable organization. For more information about the FNIH, please visit fnih.org .
About the Accelerating Medicines Partnership®:
Launched in 2014 and managed by the FNIH, the Accelerating Medicines Partnership (AMP) program brings together the National Institutes of Health, U.S. Food and Drug Administration, biomedical and life sciences companies, nonprofits, patient-focused groups, and other organizations to transform the current model for developing new diagnostics and treatments. Using cutting-edge scientific approaches and broad sharing of research data, all AMPs seek to improve understanding of disease pathways, facilitate better selection of targets for drug development, and streamline processes for bringing new treatments to patients. To learn more about AMP,
visit fnih.org/AMP.
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