Status:
TERMINATED
A Study of ALG-010133 Drug to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics After Single and Multiple Doses in Healthy Volunteers and CHB Subjects
Lead Sponsor:
Aligos Therapeutics
Conditions:
Chronic Hepatitis B
Eligibility:
All Genders
18-70 years
Phase:
PHASE1
Brief Summary
A Randomized Study of ALG-010133 Drug to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics After Single and Multiple Doses in Healthy Volunteers and CHB Subjects
Eligibility Criteria
Inclusion
- Inclusion Criteria for Healthy Subjects:
- Male and Female between 18 and 55 years old
- Female subjects must have a negative serum pregnancy test at screening
- Subjects must be nonsmokers for at least 3 months prior to randomization
- BMI 18.0 to 32.0 kg/m\^2
- Subjects must have a 12-lead ECG that meets protocol criteria
- Inclusion Criteria for CHB Subjects:
- Male and Female between 18 and 70 years old
- Female subjects must have a negative serum pregnancy test at screening
- BMI 18.0 to 35.0 kg/m\^2
- HBeAg-negative chronic hepatitis B or HBeAg-positive chronic hepatitis B and are currently receiving HBV NA treatment for ≥6 months prior to screening
- Subjects must have a 12-lead ECG that meets protocol criteria
- Exclusion Criteria for Healthy Subjects:
- 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
- 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.
- Subjects with a history of clinically significant drug allergy
- Subject with current or history of clinically significant (as determined by the Investigator) skin disease requiring intermittent or chronic treatment
- Excessive use of alcohol defined as regular consumption of ≥14 units/week for women and ≥21 units/week for men
- Unwilling to abstain from alcohol use for 48 hours prior to start of dosing through end of study follow up
- Subjects with Hepatitis A, B, C, D, E or HIV-1/HIV-2 infection or acute infections such as SARS- CoV-2 infection
- 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)
- Exclusion Criteria for CHB Subjects:
- 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
- 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.
- Subjects with a history of clinically significant drug allergy
- Subject with current or history of clinically significant (as determined by the Investigator) skin disease requiring intermittent or chronic treatment
- Excessive use of alcohol defined as regular consumption of ≥14 units/week for women and ≥21 units/week for men
- Subjects with Hepatitis A, C, D, E or HIV-1/HIV-2 infection or acute infections such as SARS- CoV-2 infection
- 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)
- Subject with any history or current evidence of hepatic decompensation such as: variceal bleeding, spontaneous bacterial peritonitis, ascites, hepatic encephalopathy, or active jaundice (within the last year)
- Subjects must have absence of signs of hepatocellular carcinoma
- Subjects with history or current liver cirrhosis
- Subjects positive for anti-HBs anitbodies
- Subjects with liver fibrosis that is classified as Metavir Score ≥F3
Exclusion
Key Trial Info
Start Date :
August 17 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 8 2022
Estimated Enrollment :
103 Patients enrolled
Trial Details
Trial ID
NCT04485663
Start Date
August 17 2020
End Date
March 8 2022
Last Update
March 15 2022
Active Locations (10)
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1
Nanfang Hospital of Southern Medical University
Guangzhou, Guangdong, China
2
The First Hospital of Jilin University
Changchun, Jilin, China, 130021
3
Queen Mary Hospital
Hong Kong, Hong Kong
4
PMSI Republican Clinical Hospital "T. Mosneaga", ARENSIA Exploratory Medicine Phase I Unit
Chisinau, Moldova