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Trial registered on ANZCTR


Registration number
ACTRN12623000111673p
Ethics application status
Submitted, not yet approved
Date submitted
13/01/2023
Date registered
1/02/2023
Date last updated
31/08/2023
Date data sharing statement initially provided
1/02/2023
Type of registration
Prospectively registered

Titles & IDs
Public title
An optional multicenter, open-label Phase 2a multiple dose study in Chronic Hepatitis B (CHB) subjects to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of BJT-778
Scientific title
A Phase 1/2a, Randomized, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of BJT-778 in Healthy Volunteers and in Subjects with Chronic Hepatitis B Infection, Including Subjects with Chronic Hepatitis D Infection- Part 4 conducted in individuals with chronic hepatitis B infection.
Secondary ID [1] 308344 0
BJT-778-001
Universal Trial Number (UTN)
Trial acronym
Linked study record
This study follows up from ACTRN12623000075684, ACTRN12623000078651, and ACTRN12623000105640.

Health condition
Health condition(s) or problem(s) studied:
Chronic Hepatitis B Virus (HBV) Infection 328134 0
Condition category
Condition code
Infection 325190 325190 0 0
Other infectious diseases
Oral and Gastrointestinal 325559 325559 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
BJT-778 is being developed as a potent, selective neutralizing monoclonal antibody for the treatment of Chronic Hepatitis B Virus Infection (CHB) and Chronic Hepatitis D Virus Infection (CHD).
Cohort E: Once the safety and antiviral activity in Cohort B +/- C are established for a given dose (i.e., Dose 1), optional open-label multidose BJT-778 cohorts may be initiated including different dosing intervals (i.e., every 1, 2 or 4 weeks). The decision to initiate multidose cohorts for a given dose (i.e., Dose 1) will be determined by safety and maximum HBsAg reductions observed with a single dose.
Subjects will be monitored with serial vitals, ECGs, safety laboratory assessments, and AEs recording.
The number of subjects per cohort in Cohort E is targeted at 8 but may be expanded to enable all qualifying subjects in Cohort B and C the opportunity to enroll.
For a given dose (i.e., Dose 1), arms exploring different intervals may enroll simultaneously or sequentially at the discretion of the Sponsor. No subjects in Cohort E will receive placebo.
• E1) Optional Dose considered safe in Cohort B +/- C, given subcutaneously at a TBD interval for 12 weeks
• E2) Optional Dose considered safe in Cohort B +/- C, given subcutaneously at a TBD interval for 12 weeks
• E3) Optional Dose considered safe in Cohort B +/- C, given subcutaneously at a TBD interval for 12 weeks
All Subjects will continue their nucleos(t)ide treatment for the duration of the study including the follow up.
Doses fall within the range of 75mg to 900mg and the exact doses will be disclosed after IP restrictions are met.
Intervention code [1] 324794 0
Treatment: Drugs
Comparator / control treatment
No control group.
Control group
Uncontrolled

Outcomes
Primary outcome [1] 333016 0
To evaluate the safety and tolerability of BJT-778. Subjects will be monitored with serial vitals, ECGs, safety labs, and adverse events recording from Screening to End of Treatment.
Timepoint [1] 333016 0
Participants will be assessed daily for adverse events from baseline to end of treatment visit. Adverse events are recorded using Division of AIDS Adverse Experience Reporting System (DAERS) from Screening to Day 169. Some of the known/possible adverse events are Immune-complex disease, changes in liver function/liver related blood tests and risk of allergic reactions.
Safety labs are collected regularly throughout the study from screening up to 24 weeks, these include
Blood chemistries, Hematology, Complement studies (C3, C5a, Bb) and Urinalysis.
Blood samples for Blood chemistries, Hematology, are collected at screening and Days 1, 8, 15, 29, 43, 57, 71, 85, 113, 141 and Day 169 post-dose for Cohort E.
Blood samples for complement studies (C3, C5a, Bb) are collected at screening and Days 1, 8, 15, 29, 43, 57, 71, 85, 113, 141 and Day 169 post-dose for Cohort E as well as at any time post-dose if immune-complex disease is suspected.
Urine samples are collected screening, Days 1, 8, 15, 29, 43, 57, 71, 85, 113, 141 and Day 169 post-dose for Cohort E.
Vital signs will be collected at every visit – heart rate measured using a pulse oximeter, blood pressure measured using a sphygmomanometer, temperature measured using a thermometer and respiratory rate counted by qualified personnel - all will be performed before blood draws from Screening to Day 169 post dose.
Supine ECGs will be performed before blood draws in Screening.
Secondary outcome [1] 415555 0
To evaluate the plasma pharmacokinetics of BJT-778. PK parameters include but are not limited to Cmax, Clast, Tmax, Tlast, AUCinf, AUClast, t1/2, Lambda z, WF, and CL/F
Timepoint [1] 415555 0
PK blood samples are collected as follows:
• Cohort E: Day 1 (pre-dose), Days 8, 15, 29, 43, 57, 71, 85, 113, 141, and 169
Secondary outcome [2] 415999 0
To evaluate the immunogenicity of BJT-778 by assessing levels of anti-drug antibodies (ADAs)
Timepoint [2] 415999 0
Blood samples are collected at regular intervals - once on Day 1, 15, 29, 57, 85, 169 post-dose for Cohort E and stored for analysis of ADAs.
Secondary outcome [3] 416927 0
To evaluate the anti-viral activity of BJT-778 by assessing HBsAg levels
Timepoint [3] 416927 0
Participants will be assessed for changes in absolute HbsAg levels or Anti-HBsAg activity. 2 blood samples for quantitative HBsAg measurements are collected regularly throughout treatment and follow up i.e.,
For Cohort E: twice on Day 1, 8, 15, 29, 43, 57, 71, 85, 113, 141, 169 post-dose

Eligibility
Key inclusion criteria
• Male or female adults between 18 and 70 years of age
• BMI 18 to 40 kg/m2
• Chronic HBV infection greater than or equal to 6 months (e.g., positive for serum HBsAg greater than or equal to 6 months)
• Plasma HBV DNA less than 100 IU/ml at Screening
• On nucleos(t)ide analogs
• Qualitative HBsAg level criteria at Screening by Cohort/group:
- Cohort E: greater than or equal to 10 IU/ml
Minimum age
18 Years
Maximum age
70 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
• Evidence of cirrhosis
• History of decompensated liver disease
• History of liver disease other than Hepatitis B
• Received solid organ or bone marrow transplant
• Currently taking, or took within 1 month of Screening, any immunosuppressing drugs (e.g., prednisone). If the subject received a short course, the situation may be discussed with the Medical Monitor, or designee
• Clinically significant abnormalities aside from chronic HBV infection in medical history (e.g., previous acute coronary syndrome within 6 months of Screening, major surgery within 3 months of Screening, uncontrolled diabetes) or physical examination
• History of bleeding diathesis or coagulopathy
• History of, or suspected presence of vasculitis
• History of extrahepatic disorders possibly related to HBV immune complexes (e.g., glomerulonephritis, polyarteritis nodosa)
• Malignancy within 5 years, except for basal or squamous cell carcinoma of the skin or carcinoma in situ of the cervix that has been successfully treated
• Treatment with a different investigational drug other than BJT-778, biological agent, or device within 4 weeks of screening or 5 half-lives of Study Drug, whichever is longer.
• History of drug abuse/addiction within 6 months (except cannabis) of Screening or positive urine drug Screen (excluding physician-prescribed drugs and cannabis)
• Unwillingness to comply with study procedures, including follow-up, as specified by this protocol, or unwillingness to cooperate fully with the Investigator
• Have any other conditions (medical, social, psychiatric, or other), which in the opinion of the Investigator would make the subject unsuitable for inclusion or could interfere with the subject participating in or completing the study.

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised 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
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 2
Type of endpoint/s
Safety
Statistical methods / analysis

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
11/09/2023
Actual
Date of last participant enrolment
Anticipated
31/01/2024
Actual
Date of last data collection
Anticipated
18/07/2024
Actual
Sample size
Target
24
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,VIC
Recruitment hospital [1] 23504 0
Royal Prince Alfred Hospital - Camperdown
Recruitment hospital [2] 23505 0
The Alfred - Melbourne
Recruitment hospital [3] 23664 0
St Vincent's Hospital (Melbourne) Ltd - Fitzroy
Recruitment postcode(s) [1] 38912 0
2050 - Camperdown
Recruitment postcode(s) [2] 38913 0
3004 - Melbourne
Recruitment postcode(s) [3] 39087 0
3065 - Fitzroy

Funding & Sponsors
Funding source category [1] 312587 0
Commercial sector/Industry
Name [1] 312587 0
Bluejay Therapeutics Inc.
Country [1] 312587 0
United States of America
Primary sponsor type
Commercial sector/Industry
Name
Bluejay Therapeutics Inc.
Address
400 Concar Drive, Suite 3-101, San Mateo, CA 94402
Country
United States of America
Secondary sponsor category [1] 314202 0
None
Name [1] 314202 0
Address [1] 314202 0
Country [1] 314202 0
Other collaborator category [1] 282474 0
Commercial sector/Industry
Name [1] 282474 0
Novotech (Australia) Limited
Address [1] 282474 0
Novotech (Australia) Pty Limited
Level 3, 235 Pyrmont Street Sydney, NSW, Australia - 2009
Country [1] 282474 0
Australia

Ethics approval
Ethics application status
Submitted, not yet approved
Ethics committee name [1] 311914 0
Central Health and Disability Ethics Committees (HDEC)
Ethics committee address [1] 311914 0
Ethics committee country [1] 311914 0
New Zealand
Date submitted for ethics approval [1] 311914 0
01/11/2022
Approval date [1] 311914 0
15/11/2022
Ethics approval number [1] 311914 0
2022 FULL 13730

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

Contacts
Principal investigator
Name 122818 0
Prof Ed Gane
Address 122818 0
New Zealand Clinical Research 3 Ferncroft St, Grafton Auckland 1010 New Zealand
Country 122818 0
New Zealand
Phone 122818 0
+64 021548371
Fax 122818 0
Email 122818 0
[email protected]
Contact person for public queries
Name 122819 0
Carole Ann Moore
Address 122819 0
Vice President, Clinical Operations, 400 Concar Drive, Suite 3-101, San Mateo, CA 94404
Country 122819 0
United States of America
Phone 122819 0
+001 650 796 5003
Fax 122819 0
Email 122819 0
[email protected]
Contact person for scientific queries
Name 122820 0
Nancy Shulman, MD
Address 122820 0
Nancy Shulman, MD
Chief Medical Officer
951 Mariners Island Blvd., Suite 300
San Mateo, CA 94404
Country 122820 0
United States of America
Phone 122820 0
+0016506650669
Fax 122820 0
Email 122820 0
[email protected]

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

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.