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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT05414981




Registration number
NCT05414981
Ethics application status
Date submitted
2/06/2022
Date registered
10/06/2022

Titles & IDs
Public title
A Study to Assess the Safety, Pharmacokinetics, and Antiviral Activity of ABI-H3733 in Subjects With Chronic Hepatitis B Virus Infection
Scientific title
A Randomized, Blinded, Placebo-Controlled, Dose-Ranging Phase 1b Study of the Safety, Pharmacokinetics, and Antiviral Activity of ABI-H3733 in Subjects With Chronic Hepatitis B Virus Infection
Secondary ID [1] 0 0
2022-000318-32
Secondary ID [2] 0 0
ABI-H3733-102
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Chronic Hepatitis B 0 0
Condition category
Condition code
Infection 0 0 0 0
Other infectious diseases
Oral and Gastrointestinal 0 0 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - ABI-H3733
Treatment: Drugs - Placebo

Active comparator: ABI-H3733 -

Placebo comparator: Placebo -


Treatment: Drugs: ABI-H3733
25 mg or 100 mg tablets for oral administration

Treatment: Drugs: Placebo
25 mg or 100 mg tablets for oral administration
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Proportion of subjects with adverse events (AEs), premature treatment discontinuation due to AEs, and abnormal laboratory results
Timepoint [1] 0 0
Through end of study, up to 56 days
Secondary outcome [1] 0 0
Maximum Plasma Concentration (Cmax) of ABI-H3733 in subjects with cHBV
Timepoint [1] 0 0
Through treatment period, up to 28 days
Secondary outcome [2] 0 0
Minimum Plasma Concentration (Cmin) of ABI-H3733 in subjects with cHBV
Timepoint [2] 0 0
Through treatment period, up to 28 days
Secondary outcome [3] 0 0
Area Under Plasma Concentration-Time Curve (AUC) of ABI-H3733 in subjects with cHBV
Timepoint [3] 0 0
Through treatment period, up to 28 days
Secondary outcome [4] 0 0
Time to Maximum Plasma Concentration (Tmax) of ABI-H3733 in subjects with cHBV
Timepoint [4] 0 0
Through treatment period, up to 28 days
Secondary outcome [5] 0 0
Elimination half-life (t1/2) of ABI-H3733 in subjects with cHBV
Timepoint [5] 0 0
Through treatment period, up to 28 days
Secondary outcome [6] 0 0
To evaluate the effect of food on Cmax of ABI-H3733 in subjects with cHBV
Timepoint [6] 0 0
Through treatment period, up to 28 days
Secondary outcome [7] 0 0
To evaluate the effect of food on AUC of ABI-H3733 in subjects with cHBV
Timepoint [7] 0 0
Through treatment period, up to 28 days
Secondary outcome [8] 0 0
To evaluate the effect of food on the proportion of subjects with AEs, premature discontinuation due to AEs and abnormal laboratory results
Timepoint [8] 0 0
Through treatment period, up to 28 days
Secondary outcome [9] 0 0
To evaluate the changes in HBV DNA (IU/mL or Log IU/mL) in subjects with cHBV by Quantitative PCR
Timepoint [9] 0 0
Through treatment period, up to 28 days

Eligibility
Key inclusion criteria
1. Body mass index (BMI) = 18.0 and < 35.0 kg/m(2), where BMI = weight (kg)/(height [m])(2) with a minimum body weight of 45 kg.
2. Chronic hepatitis B infection, defined as HBV infection for =6 months documented
3. Treatment-naïve or off-antiviral therapy for =24 weeks prior to Screening
4. Lack of bridging fibrosis or cirrhosis
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Co-infection with human immunodeficiency virus (HIV), hepatitis C virus (HCV), hepatitis D virus (HDV), acute hepatitis A virus (HAV), or acute hepatitis E virus (HEV)
2. History of liver transplant or evidence of advanced liver disease, cirrhosis, or hepatic decompensation
3. Clinically significant diseases or conditions
4. History of hepatocellular carcinoma
5. Current or prior treatment for cHBV

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s

The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
7/08/2022
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
24/04/2023
Sample size
Target
Accrual to date
Final
31
Recruitment in Australia
Recruitment state(s)
Recruitment outside Australia
Country [1] 0 0
Bulgaria
State/province [1] 0 0
Sofia City
Country [2] 0 0
Bulgaria
State/province [2] 0 0
Sofia
Country [3] 0 0
Hong Kong
State/province [3] 0 0
Hong Kong
Country [4] 0 0
Moldova, Republic of
State/province [4] 0 0
Chisinau
Country [5] 0 0
New Zealand
State/province [5] 0 0
Auckland
Country [6] 0 0
Romania
State/province [6] 0 0
Bucharest
Country [7] 0 0
Singapore
State/province [7] 0 0
Singapore

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Assembly Biosciences
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT05414981