A Relative Bioavailability and Bioequivalence Study of Varegacestat in Healthy Participants

Recruiting now · Phase 1

Conditions studied: Healthy

In brief

This is an open-label, randomized, crossover study to evaluate the relative bioavailability (rBA) and bioequivalence (BE) of a test capsule formulation of varegacestat compared to reference capsules formulation under fasting conditions.

Key facts

Study ID

NCT07610005

Run by

Immunome, Inc.

People needed

20

Starts

2026-05-21

Expected to finish

2026-06-01

Last updated by the study team

2026-06-08

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy, adult, female of non childbearing potential or male, 18 to 55 years of age, inclusive, at the screening visit
• Male participants must follow protocol-specified contraception guidance
• Continuous non-smoker who has not used nicotine and tobacco containing products for at least 3 months prior to the first dosing
• BMI ≥ 18.0 and ≤ 32.0 kg/m2 and with a body weight > 50 kg at the screening visit
• Medically healthy with no clinically significant medical history, physical examination, clinical laboratory profiles, vital signs, and ECGs, as deemed by the PI or designee
• Able to swallow multiple capsules

You may not qualify if…

• Is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or expected during the conduct of the study
• History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI or designee
• History of any illness that, in the opinion of the PI or designee might confound the results of the study or poses an additional risk to the participant by their participation in the study
• History or presence of alcohol or drug abuse within the past 2 years prior to the first dosing
• History or presence of hypersensitivity or idiosyncratic reaction to varegacestat or related compounds
• History or presence of:
• Autoimmune disease such as rheumatoid arthritis or systemic lupus erythematosus
• Thrombophlebitis or deep vein thrombosis
• Hematologic or coagulation disorders
• Liver disease or dysfunction; Gilbert's syndrome
• Renal dysfunction or glomerulonephritis
• Cancer (except treated basal cell carcinoma of the skin and cancer-free for 5 years, non metastatic basal or squamous cell carcinoma of the skin, and cervical carcinoma in situ)
• Clinically significant cardiovascular, gastrointestinal, pulmonary, endocrine, central nervous system disorders, or other major active and uncontrolled disease in the opinion of the PI or designee.

Where it is running

• Celerion, Inc. — Tempe, Arizona, United States (enrolling)

Full record on ClinicalTrials.gov

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