Overview
A Study of ALG-055009 in Healthy Volunteers and Subjects With Hyperlipidemia
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2022-09-01
2022-09-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
A Randomized Study of ALG-055009 Drug to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Multiple Doses in Healthy Volunteers and Subjects with HyperlipidemiaPhase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Aligos Therapeutics
Criteria
Inclusion Criteria for Healthy Subjects:1. Male and Female between 18 and 55 years old
2. BMI 18.0 to 32.0 kg/m^2
Inclusion Criteria for Subjects with Mild Hyperlipidemia:
1. Male and Female between 18 and 65 years old
2. BMI 18.0 to 35.0 kg/m^2
3. Subject must be on a stable diet for the 3 months prior to screening with a fasting
LDL-C level >110 mg/dL at screening
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 Hepatitis A, B, C or HIV-1/HIV-2 infection or acute infections such as
SARS- CoV-2 infection
3. 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)
4. Subjects with history of thyroid disorder or abnormal thyroid function tests at
screening or known sensitivity to thyroid medications
5. Subjects receiving, or urgently requiring, any lipid lowering therapy