Trials
Search / Trial NCT05657691

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

Xanamem Ue2343 Actinogen Cortisol 11β Hsd1 11 Beta Hydroxysteroid Dehydrogenase Type 1 Emestedastat

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.

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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