Overview
A Study to Assess Adverse Events and How Single and Multiple Ascending Doses of ABBV-903 Move Through the Body in Healthy Adults
Status:
Recruiting
Recruiting
Trial end date:
2023-05-15
2023-05-15
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to evaluate adverse events and tolerability of single and multiple doses of ABBV-903, and to assess how the drug moves through the body in healthy adult volunteers.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
AbbVieTreatments:
Itraconazole
Criteria
Inclusion Criteria:- Body Mass Index (BMI) is => 18.0 to <= 32 kg/m2 after rounded to the nearest tenth, at
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 electrocardiogram
(ECG).
Exclusion Criteria:
- History of any clinically significant illness/infection/major febrile illness,
hospitalization, or any surgical procedure within 30 days prior to the first dose of
study drug.
- History of epilepsy, any clinically significant cardiac, respiratory (except mild
asthma as a child), renal, hepatic, gastrointestinal, hematologic or psychiatric
disease or disorder, or any uncontrolled medical illness.
- 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.