Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:02 PM
Ignite Modification Date:
2025-12-24 @ 7:02 PM
NCT ID:
NCT06641557
Eligibility Criteria:
Inclusion Criteria:
* 1\. Subject must have all questions about the study answered and must have signed the informed consent document before any study-specific procedures are performed.
2\. Men or women aged 45 to 70 years at screening (both inclusive) of any race. 3. Subjects must be otherwise healthy and ambulatory, with no history or evidence of clinically relevant medical disorders 4. Mini Mental State Examination (MMSE) ≥ 28 5. Physical examination, clinical laboratory values, vital signs, and the electrocardiogram (ECGs) are clinically acceptable to the Investigator. Body weight ≥ 45 kg. Body Mass Index (BMI) ≥ 18 and ≤33 kg/m2.
6\. Female subjects must be postmenopausal or surgically sterile or sterile for other medical reason.
7\. Male subjects must agree to practice an acceptable method of highly effective birth control.
8\. Males must be willing to abstain from sperm donation from the screening visit, while on study and through 30 days after receiving the last dose of study drug.
Exclusion Criteria:
* 1\. Clinically significant abnormal values for hematology, clinical chemistry or urinalysis at the screening and admission visits.
2\. Clinically significant abnormal findings on physical examination or 12-lead electrocardiogram (ECG) at the screening or admission visits.
3\. Significant history (within six months prior to receiving the study drug) and/or presence of clinically significant medical, surgical or psychiatric disorder in the judgement of the investigator.
4\. History of clinically significant problems in the retina as reported by a subject
5\. eGFR \< 60 mg/mL
6\. Creatinine, Amylase and/or Lipase \> ULN
7\. Any malignancy in the 5 years prior to screening excluding basal cell carcinoma or squamous cell carcinoma of the skin or cervical carcinoma in situ that have been successfully treated.
8\. Any subject with a history, presence and/or current evidence of serologic positive result for hepatitis B surface antigen, hepatitis C antibodies, or HIV antibodies 1 or 2. Subjects considered to be cured for hepatitis C will be eligible.
9\. Recent history (within previous six months prior to screening) of alcohol or drug abuse (as judged by the investigator) or has consumed \> 2 alcohol drinks/day during the last three months prior to screening.
10\. Any subject with known hypersensitivity to IkT-148009. 11. Donation of blood, plasma, or acute loss of blood within 60 days prior to screening visit.
12\. Use of tobacco or nicotine-containing products during the 60 days prior to screening and for the duration of the study.
13\. Any subject who has received treatment with an investigational drug during the 30 days prior to screening.
14\. Investigative site personnel or their immediate families (spouse, parent, child or sibling whether biological or legally adopted).
15\. Any subject unwilling or unable to comply with study procedures.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
45 Years
Maximum Age:
70 Years
Study:
NCT06641557
Study Brief:
Protocol Section:
NCT06641557