A Study to Assess the Adverse Events and How Oral Emraclidine Moves Through the Body of Healthy Elderly Adult Participants
Recruiting now · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteer
In brief
This study is to assess how oral emraclidine moves through the body of healthy elderly adult participants, and assess adverse events, and tolerability.
Key facts
- Study ID
- NCT07219030
- Run by
- AbbVie
- People needed
- 40
- Starts
- 2025-10-08
- Expected to finish
- 2027-03-01
- Last updated by the study team
- 2026-05-12
Who can join
Age: 65 and older, up to 85. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- BMI is ≥ 18.0 to ≤ 32.0 kg/m2 after rounding to the tenths decimal at Screening. BMI is calculated as weight in kg divided by the square of height measured in meters.
- Body weight > 45 kg at the time of screening and upon initial confinement.
- A condition of general good health, based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead ECG.
You may not qualify if…
- History of any clinically significant cardiac, respiratory (except mild asthma as a child), renal, hepatic, gastrointestinal, genitourinary, immunological, hematologic, neurological or psychiatric disease or disorder, or any other uncontrolled medical illness.
- History of any clinically significant sensitivity or allergy to any medication or food.
- Evidence of dysplasia or history of malignancy (including lymphoma and leukemia) other than successfully treated non-metastatic cutaneous squamous cell, basal cell carcinoma or localized carcinoma in situ of the cervix.
Where it is running
- Altasciences Clinical Los Angeles /ID# 276854 — Cypress, California, United States (enrolling)
- K2 Medical Research, LLC /ID# 276636 — Maitland, Florida, United States (enrolling)
- Clinical Pharmacology Of Miami /ID# 276856 — Miami, Florida, United States (enrolling)
- Acpru /Id# 276996 — Grayslake, Illinois, United States (enrolling)
Full record on ClinicalTrials.gov
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