Xanamem® in Adults with Major Depressive Disorder and Impaired Cognition (XanaCIDD)
Launched by ACTINOGEN MEDICAL · Dec 11, 2022
Trial Information
Current as of February 05, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Key Inclusion Criteria:
- • Male or female aged 18 to 75, inclusive.
- • Positive MDD primary diagnosis confirmed by the Mini-International Neuropsychiatric Interview (MINI).
- • Persistent depressive symptoms as determined by a Hamilton Depression Rating Scale (HAM-D) ≥ 17 at Screening.
- • Cognitive abilities on a coding test \> 0.5 standard deviations below expected.
- • Self-reported subjective cognitive dysfunction.
- • Currently or previously treated with a stable dose of a first- or second-line antidepressant that is approved for the treatment of depression (but not a tricyclic antidepressant, monoamine oxidase inhibitor, or vortioxetine). If on current treatment, dose must be stable for at least 6 weeks.
- • Smokers are eligible if they are able to comfortably abstain from nicotine for 2 hours prior to scheduled cognitive assessments.
- • Able to comfortably abstain from caffeine intake for 4 hours prior to scheduled cognitive assessments.
- • Must provide written informed consent to participate in the trial and be willing and able to comply with the requirements of the protocol and complete all trial visits.
- Key Exclusion Criteria:
- • Active suicidal ideation within the previous 3 months
- • On a tricyclic antidepressant, monoamine oxidase inhibitor, esketamine, or vortioxetine.
- • A history of clinically diagnosed dementia of any type
- • Previous clinically significant systemic illness or infection, including test positive COVID-19, within the past 4 weeks prior to Screening
- • Has a BMI or body weight that will interfere with participation in the trial
- • Type I or Type II diabetes requiring insulin
- • Clinically significant ECG abnormalities
- • Participation in another clinical trial of a drug or device
- • Trial participants who in the opinion of the Investigator exhibit physical, cognitive, or language impairments of such severity as to adversely affect the validity of the data derived from the neuropsychological tests.
- • Positive testing for HIV, hepatitis B surface antigen, or hepatitis C antibodies at Screening.
- • Participants with a history of drug abuse or addiction in the past 2 years
- • Current use of cannabis/marijuana, or tetrahydrocannabinol-containing medications.
About Actinogen Medical
Actinogen Medical is a clinical research organization dedicated to advancing innovative therapies for cognitive disorders, particularly Alzheimer’s disease and other age-related dementias. With a focus on developing novel treatments that target underlying disease mechanisms, Actinogen leverages cutting-edge science and technology to enhance patient outcomes. The company is committed to conducting rigorous clinical trials that adhere to the highest ethical standards, ensuring the safety and well-being of participants while contributing to the global understanding of neurological health. Through strategic partnerships and a multidisciplinary approach, Actinogen Medical aims to bring transformative solutions to the field of neurodegenerative diseases.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Manchester, , United Kingdom
Melbourne, Victoria, Australia
London, , United Kingdom
Motherwell, , United Kingdom
Adelaide, South Australia, Australia
Melbourne, Victoria, Australia
Camberwell, Victoria, Australia
Canberra, Australian Capital Territory, Australia
Blacktown, New South Wales, Australia
Botany, New South Wales, Australia
Kanwal, New South Wales, Australia
Newcastle, New South Wales, Australia
Brisbane, Queensland, Australia
Sippy Downs, Queensland, Australia
Noble Park, Victoria, Australia
London, , United Kingdom
Tankersley, , United Kingdom
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0
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