A Study to Assess the Safety, Tolerability, and Pharmacokinetics of GIGA-2339 in Participants With Chronic Hepatitis B Virus Infection

NCT ID: NCT07024641

Last Updated: 2026-01-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE1

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-11-13

Study Completion Date

2027-09-30

Brief Summary

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The primary purpose of this study is to assess the safety and tolerability of single and multiple intravenous (IV) doses of GIGA-2339 in participants with chronic Hepatitis B Virus (HBV) infection.

Detailed Description

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Conditions

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Hepatitis B Virus Infection

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Part 1: Single Ascending Dose (SAD)

Participants will receive a single IV infusion of either GIGA-2339 or placebo in ascending doses on Day 1.

Group Type EXPERIMENTAL

GIGA-2339

Intervention Type DRUG

Administered by intravenous infusion

Placebo

Intervention Type DRUG

Administered by intravenous infusion

Part 2: Multiple Ascending Dose (MAD)

Participants will receive multiple IV infusions of either GIGA-2339 or placebo, once every 4 weeks, at a dose determined in Part 1.

Group Type EXPERIMENTAL

GIGA-2339

Intervention Type DRUG

Administered by intravenous infusion

Placebo

Intervention Type DRUG

Administered by intravenous infusion

Interventions

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GIGA-2339

Administered by intravenous infusion

Intervention Type DRUG

Placebo

Administered by intravenous infusion

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Hepatitis B envelope antigen (HBeAg) negative chronic HBV infection for ≥ 6 months, defined as presence of Hepatitis B surface antigen (HBsAg) in serum for ≥ 6 months.
* Serum HBsAg concentration between ≥ 100 international units per milliliter (IU/mL) and 2000 IU/mL at screening.
* Currently on stable dose of nucleot(s)ide analogues (NAs) (≥ 6 months) and expected to continue while participating in the study, or are not received NAs.
* Have serum HBV deoxyribonucleic acid (DNA) concentration ≤ 50 IU/mL at screening (for those who are on NAs); or have serum HBV DNA concentration ≤ 2000 IU/mL at screening (for those who are NOT on NAs).
* Male participants must refrain from donating spermatozoa and agree to use highly effective contraception.
* Female participants must not be pregnant, or breastfeeding; either should not be a woman of childbearing potential (WOCBP) or if WOCBP should use highly effective contraceptive methods.

Exclusion Criteria

* Positive for co-infection with hepatitis C virus (HCV), human immunodeficiency virus (HIV), and/or hepatitis D virus (HDV) at screening.
* Participants that weigh less than 50 kilograms (kg) and/or have a body mass index (BMI) less than 18.5.
* History of documented liver cirrhosis at screening. Patients under liver cirrhosis evaluation at screening will not be eligible until cirrhosis is ruled out.
* Liver stiffness \> 8 kilopascal (kPa) at screening.
* History of chronic liver disease from another cause, immune complex disease, or autoimmune diseases that in the opinion of the investigator would preclude participation.
* Family history of hepatocellular carcinoma (HCC).
* Alpha fetoprotein \> 20 nanograms per milliliter (ng/mL).
* Presence of a liver imaging reporting and data system (LI-RADS) 4 or 5 liver lesion on imaging 12 months prior to Screening OR, LI-RADS-US findings of US-3 grade on imaging 12 months prior to Screening, OR LIRADS-US grade 3 done prior to the D1 infusion visit, if prior LI-RADS or LI-RADS-US results are not available at Screening.
* History of hematopoietic stem cell transplant or solid organ transplant.
* Receipt of anti-HBV monoclonal antibody (mAb)/pAb therapy of any kind in the past (including hepatitis B immunoglobulin \[HBIG\]).
* History of cardiovascular disease (e.g., coronary artery disease, cardiomyopathy, congestive heart failure, family history of congenital long QT syndrome). Stable hypertension is allowed.
* Malignancy diagnosed and/or treated within 5 years prior to Screening, and/or with ongoing treatment for malignancy, with the exception of localized non-metastatic basal cell or squamous cell carcinoma of the skin or in-situ carcinoma of the cervix excised with curative intent.
* Participants requiring anti-coagulation therapies (for example warfarin, Factor Xa inhibitors, or anti-platelet agents like clopidogrel).
* Male participants with a corrected QT interval using Fridericia's formula (QTcF) \> 450 milliseconds (msec) and female participants with QTcF \> 470 msec on ECG recorded at screening. if the participant has evidence of an intraventricular conduction delay, defined as QRS interval greater than 110 msec, a QTcF is \> 500 msec for both males and females will be excluded.
* Known hypersensitivity to any GIGA-2339 excipients or any confirmed significant allergic reactions (urticaria or anaphylaxis) against any drug, or multiple drug allergies (nonactive hay fever is acceptable), or a history of drug or other allergy that, in the opinion of the Investigator, contraindicates participation.
* Received or will receive live-attenuated virus vaccinations such as measles, mumps, rubella or varicella within 4 weeks before and up to three months after administration of investigational product (IP).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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GigaGen, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Grifols Investigative site

Chandler, Arizona, United States

Site Status RECRUITING

Grifols Investigative site

Huntington Beach, California, United States

Site Status RECRUITING

Grifols Investigative site

Lake Forest, California, United States

Site Status RECRUITING

Grifols Investigative site

Long Beach, California, United States

Site Status RECRUITING

Grifols Investigative site

Oakland, California, United States

Site Status RECRUITING

Grifols Investigative Site

Peachtree Corners, Georgia, United States

Site Status RECRUITING

Grifols Investigative Site

Iowa City, Iowa, United States

Site Status RECRUITING

Grifols Investigative Site

Lenexa, Kansas, United States

Site Status RECRUITING

Grifols Investigative site

Baltimore, Maryland, United States

Site Status RECRUITING

Grifols Investigative site

San Antonio, Texas, United States

Site Status RECRUITING

Grifols Investigative site

Webster, Texas, United States

Site Status RECRUITING

Grifols Investigative site

Richmond, Virginia, United States

Site Status RECRUITING

Grifols Investigate Site

Concord, New South Wales, Australia

Site Status RECRUITING

Grifols Investigative site

Fortitude Valley, Queensland, Australia

Site Status RECRUITING

Countries

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United States Australia

Central Contacts

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Enrikas Vainorius, MD

Role: CONTACT

+1 919-316-6396

Facility Contacts

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Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Enrikas Vainorius, MD

Role: primary

Other Identifiers

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GC2301

Identifier Type: -

Identifier Source: org_study_id

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