Safety and Pharmacokinetics of ALZ-507 in Healthy Elderly Adults
Alzheon Inc. · NCT07824271
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 50–75 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 84
- US sites recruiting
- 1
- Study start
- March 9, 2026
- Record last updated
- September 17, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Researchers are testing an investigational medicine called ALZ-507 in healthy adults between 50 and 75 years of age.
The purpose of this study is to learn
Assess if oral ALZ-507 is safe What side effects may occur How the body absorbs ALZ-507 Whether food affects how ALZ-507 is absorbed How much ALZ-507 reaches the blood, cerebrospinal fluid, and urine
Participants will receive either ALZ-507 or a placebo. Some participants will receive a single dose, while others will receive daily doses for two weeks. Researchers will monitor participants closely through medical examinations, laboratory testing, and collection of blood, cerebrospinal fluid and urine.
The findings from this study will help guide the future development of ALZ-507.
The information from this study will help determine whether ALZ-507 is safe for further clinical development.
Being studied: ALZ-507; Placebo
Conditions: Healthy Participants Study
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Healthy males and females aged 50 to 75 years, inclusive
- Body mass index 18.0 to 35.0 kg/m2, inclusive, and >50 kg body weight
- No clinically significant values for vital signs (systolic blood pressure [BP] 90 to 140 mmHg, diastolic BP 40 to 90 mmHg, and HR 50 to 100 bpm) and no clinically significant ECG readings, as determined by the principal investigator or sub investigator
Exclusion Criteria
- Participation in a clinical research study within the previous 30 days or within a period of less than 5 times the drug's half-life
- Have previously participated in a trial with ALZ-801 or tramiprosate and received study drug
- History of any drug or alcohol abuse in the past 2 years
- Creatinine clearance of \<60 mL/min using the Cockcroft-Gault equation at screening
- Clinically significant abnormal biochemistry, hematology or urinalysis as judged by the investigator
- History of clinically significant cardiovascular, pulmonary, chronic respiratory, renal, hepatic, GI, immunologic, endocrine, neurologic, psychiatric or thromboembolic disease; a history of metabolic disturbances; or any current physical conditions that could interfere with the interpretation of the study results as judged by the investigator
Recruiting US locations
Quotient Sciences
Miami, FL 33126
Site contact: Laura Gonzalez · 305-644-9903 · Laura.Gonzalez@quotientsciences.com
Study contacts (from the official record)
- John Hey, PhD · 508.861.7709 · john.hey@alzheon.com
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