Overview

A Study in Healthy Volunteers to Evaluate the Safety, Tolerability, Pharmacokinetics, and Drug-Drug Interaction Potential of Single and Multiple Doses of ALG-097558

Status:
Not yet recruiting
Trial end date:
2024-03-30
Target enrollment:
0
Participant gender:
All
Summary
A multi-part study of ALG-097558 to evaluate safety, tolerability, pharmacokinetics and drug-drug interaction potential after single and multiple doses in healthy volunteers
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Aligos Therapeutics
Treatments:
Carbamazepine
Itraconazole
Midazolam
Criteria
Inclusion Criteria for All Subjects:

1. Male and Female between 18 and 55 years old

2. BMI 18.0 to 32.0 kg/m^2

3. Female subjects must have a negative serum pregnancy test at screening

4. Subjects must have a 12-lead electrocardiogram (ECG) that meets the protocol criteria

Exclusion Criteria for All Subjects:

1. Subjects with any current or previous illness that, in the opinion of the
Investigator, might confound the results of the study or pose an additional risk in
administering study drug to the subject or that could prevent, limit, or confound the
protocol specified assessments or study results' interpretation

2. Subjects with a past history of cardiac arrhythmias, risk factors for Torsade de
Pointes syndrome (e.g., hypokalemia, family history of long QT Syndrome) or history or
clinical evidence at screening of significant or unstable cardiac disease etc.

3. Subjects with a history of clinically significant drug allergy

4. Excessive use of alcohol defined as regular consumption of ≥14 units/week

5. Unwilling to abstain from alcohol use for 1 week prior to start of the study through
end of study follow up

6. Subjects with Hepatitis A, B, C, E or HIV-1/HIV-2 infection or acute infections such
as SARS- CoV-2 infection

7. Subjects with renal dysfunction (e.g., estimated creatinine clearance <90 mL/min/1.73
m^2 at screening, calculated by the Chronic Kidney Disease Epidemiology Collaboration
[CKD-EPI] formula)