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

Official title

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

Overview

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.

Interventions

• Drug CORT108297
  120mg of a selective glucocorticoid receptor antagonist, taken as 2 tablets daily for 2 weeks
• Drug Placebo
  Placebo taken as 2 tablets daily for 2 weeks

Primary outcome measures

• Memory as assessed by pattern separation task performance after 2 weeks of treatment with CORT108297 [Time frame: After 2 weeks of treatment]
• Memory as assessed by the Hopkins Verbal Learning Test-Revised Edition (HVLT-R) after 2 weeks of treatment with CORT108297 [Time frame: After 2 weeks of treatment]
• Executive functioning as assessed by the Trail Making Test (TMT), part B after 2 weeks of treatment with CORT108297 [Time frame: After 2 weeks of treatment]
• Executive functioning as assessed by the Digit Span Task (digit span backwards) after 2 weeks of treatment with CORT108297 [Time frame: After 2 weeks of treatment]

Eligibility criteria

Individuals must meet criteria for mild cognitive impairment due to Alzheimer's disease according to National Institute on Aging (NIA)/Alzheimer's Association recommendations OR be cognitively normal based on clinical and cognitive assessment in the Enrollment Visit and have at least one of the following risk factors for AD:

• Known to have at least 1 apolipoprotein E (APOE) ε4 allele;
• Subjective cognitive concerns with a T score < 40 on the Multifactorial Memory Questionnaire Satisfaction Scale;
• A first-degree relative with dementia.

Inclusion Criteria for all subjects:

• At least 55 years of age;
• Body mass index >17 and <30;
• Post-menopausal (if female)
• Non-smoker;
• Availability of a study partner who has frequent contact with the subject (10+ hours/week in person and by telephone), and is able to provide an independent evaluation of functioning;
• Fluent English speaker;
• Good general health with no disease expected to interfere with the study;
• Willing and able to participate for the duration of the study.

Exclusion Criteria for all subjects:

• Participation in a therapeutic clinical trial at any time during the study;
• Abnormal corrected QT interval using Bazett's formula (QTcB; defined as > 450 ms for men and > 470 ms for women) as determined on ECG;
• Any significant neurologic disease other than suspected incipient Alzheimer's disease, such as Parkinson's disease, multi-infarct dementia, Huntington's disease, normal pressure hydrocephalus, brain tumor, progressive supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis, or history of significant head trauma followed by persistent neurologic deficits or known structural brain abnormalities, including lacunes in critical memory structures including the hippocampus and parahippocampal cortex;
• Bipolar disorder within the past 1 year;
• History of alcohol or drug dependence;
• Any significant systemic illness or unstable medical condition, which could lead to difficulty complying with the protocol;
• General surgery within the last 3 months;
• Sensory impairment (poor vision or hearing) significant enough to interfere with ability to provide valid cognitive test data;
• Treatment within the last six months with neuroleptics, sedative hypnotics, or glucocorticoids;
• Treatment within the last six months with medications metabolized by the CYP2C9 or CYP2C19 enzymes, most notably clopidogrel and proton pump inhibitors;
• Concurrent use of a CYP3A inhibitor, including grapefruit juice, and St. John's Wort;
• Exceptions to these guidelines may be considered on a case-by-case basis at the discretion of the PI.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation

Randomized

Model

Crossover

Masking

Quadruple blind

Primary purpose

Treatment

Study locations

United States · 1 center

• Johns Hopkins School of Medicine — Baltimore

Identifiers

NCT: NCT04601038 · IRB00227116

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗