Actively Recruiting

Phase 2
Age: 55Years +
All Genders
Healthy Volunteers
NCT04601038

Trial of CORT108297 to Attenuate the Effects of Acute Stress in the Allocortex (CORT-X)

Led by Johns Hopkins University · Updated on 2025-07-23

52

Participants Needed

1

Research Sites

287 weeks

Total Duration

On this page

Sponsors

J

Johns Hopkins University

Lead Sponsor

P

Private Philanthropic Funds

Collaborating Sponsor

AI-Summary

What this Trial Is About

CORT-X will examine if mitigation of stress-mediated pathogenesis of Alzheimer's disease (AD) is a feasible target for intervention in individuals at risk for this disease. This single-site (Baltimore, Maryland) phase II clinical trial is a 2-week, randomized, placebo-controlled crossover study of the effects of the selective glucocorticoid receptor antagonist, CORT108297, on cognitive test performance in 26 individuals with mild cognitive impairment (MCI) due to AD and in 26 cognitively normal individuals with an increased risk for AD due to family history, genetics, and/or subjective memory complaints. All subjects will participate in a brief stressor (public speaking and mental arithmetic) and provide saliva samples so investigators can measure stress hormone response. Then, following 2 weeks of treatment with placebo or CORT108297, in counterbalanced order, participants will complete cognitive tests assessing memory and executive function. All study participants will receive CORT108297 and placebo over the course of this 10-week trial that requires 6 in-person study visits. The primary aims will compare the effects of CORT108297 to placebo on cognitive test performance in individuals with MCI due to AD and in individuals at risk for AD, and describe the side effects of CORT108297 in study participants. Secondary aims will identify subject characteristics that predict positive response to study drug.

CONDITIONS

Official Title

Trial of CORT108297 to Attenuate the Effects of Acute Stress in the Allocortex (CORT-X)

Who Can Participate

Age: 55Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Meet criteria for mild cognitive impairment due to Alzheimer's disease OR be cognitively normal with increased risk for Alzheimer's due to family history, genetics, or memory complaints
  • At least 55 years of age
  • Body mass index greater than 17 and less than 30
  • Post-menopausal if female
  • Non-smoker
  • Have a study partner with frequent contact (10+ hours/week) who can provide independent evaluation
  • Native English speaker
  • Good general health with no disease expected to interfere with study
  • Willing and able to participate for the study duration
Not Eligible

You will not qualify if you...

  • Participation in another therapeutic clinical trial during this study
  • Abnormal corrected QT interval on ECG (QTcB > 450 ms for men, > 470 ms for women)
  • Significant neurologic diseases other than suspected early Alzheimer's disease
  • Major depression or bipolar disorder within the past year
  • History of alcohol or drug dependence
  • Significant systemic illness or unstable medical condition
  • General surgery within last 3 months
  • Significant sensory impairment affecting cognitive testing
  • Treatment within last 6 months with antidepressants, neuroleptics, sedative hypnotics, or glucocorticoids
  • Treatment within last 6 months with medications metabolized by CYP2C9 or CYP2C19 enzymes (e.g., clopidogrel, proton pump inhibitors)
  • Concurrent use of CYP3A inhibitors such as grapefruit juice or St. John's Wort
  • Exceptions may be considered case-by-case by the principal investigator

AI-Screening

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Trial Site Locations

Total: 1 location

1

Johns Hopkins School of Medicine

Baltimore, Maryland, United States, 21224

Actively Recruiting

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Research Team

N

Nicholas Bienko, MS

CONTACT

C

Cynthia A Munro, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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