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Not yet recruitingNCT07905157Updated Oct 29, 2026

A Study to Compare Blood Levels of Bepirovirsen and Safety Using Different Methods of Injecting in Healthy Adult Participants

A Phase 1 interventional study of Bepirovirsen in Hepatitis B, sponsored by GlaxoSmithKline. Not yet recruiting. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by GlaxoSmithKline · Phase 1, Interventional, and Treatment

Updated Oct 29, 2026Newly registeredGo to Updates ↓
Phase
Phase 1
Study type
Interventional
Enrollment
98
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This is an open-label study being done to compare two different methods of study medicine bepirovirsen is given in healthy adults. The researchers want to learn how the body affects the medicine over time (pharmacokinetic [PK] study). The study will also evaluate the safety of bepirovirsen and how well it is tolerated, meaning how people feel after receiving the medicine and whether they experience any side effects.

02

Conditions studied

  • Hepatitis B

Keywords

  • Bepirovirsen
  • Hepatitis B virus
  • Liver Diseases
  • Infectious Diseases
  • Pharmacokinetics
  • Administration
  • Safety
  • Autoinjector
03

In context

Hepatitis B

1,045 studies on the registry are indexed under Hepatitis B; 139 are open to participants now.

This study's planned enrollment of 98 is below the median of 147 across 756 interventional studies indexed under Hepatitis B.

Browse Hepatitis B studies →

Lead sponsor

GlaxoSmithKline is the lead sponsor of 3,650 studies on the registry; 118 are open to participants now.

Of its 264 completed or terminated interventional studies of FDA-regulated products, 241 (91%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age greater than or equal to (>=) 18 and less than or equal to (\<=) 65 years at the time of signing the .
  • Participants who are overtly healthy as determined by medical evaluation including medical history, physical examination, laboratory tests, (ECGs) and vital signs.
  • Body weight >=50 kilograms (kg) and (BMI) >= 19.0 to 29.9 kilograms per square meter (kg/m\^2).
  • Male and female participants, as follows:

    • Male Participants: There are no requirements for male participants.
    • A female participant is eligible to participate if they are not pregnant or breastfeeding, and one of the following conditions applies:

      • Is a participant of non- (PONCBP), or
      • Is a participant of childbearing potential (POCBP) and using an acceptable contraceptive method 28 days prior to and during the study intervention period and for at least 16 weeks after the last dose of study intervention. The Investigator should evaluate the potential for contraceptive method failure (for example, non-compliance, recently initiated in relationship to the first dose of study intervention).
  • Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in the protocol.

Exclusion criteria

Exclusion Criteria:

  • History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematologic, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs; constituting a risk when taking the study intervention or interfering with the interpretation of data.
  • Abnormal blood pressure, as determined by the investigator.
  • Lymphoma, leukemia, or any within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of disease for 3 years.
  • Participants with any other medical conditions which, in the judgement of the investigator (or in consultation with the Medical Monitor), could jeopardize the integrity of the safety of the participant or the data derived from that participant.
  • Current or chronic history of liver disease, hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
  • Past, current or intended use of over-the-counter or prescription medication including herbal medications within 7 days or 5 half-lives (whichever is longer) before dosing.
  • Prior use of drugs within 3 months before dosing or interferon within 12 months before dosing.
  • Prior treatment with any oligonucleotide or small interfering ribonucleic acid (siRNA) within 12 months before dosing
  • Participants for whom immunosuppressive treatment, including therapeutic doses of , is .
  • Participants requiring anti-coagulation therapies (e.g., warfarin, Factor Xa inhibitors) or anti- agents (including but not limited to clopidogrel or aspirin) unless treatment can safely be discontinued throughout duration of study intervention, by the discretion of the investigator. Occasional use is permitted.
  • Prior treatment with bepirovirsen.

Prior/Concurrent clinical study participation:

  • Loss of blood or blood products in excess of 500 milliliters (mL) within any 3-month period during the study.
  • Exposure to more than 4 new drugs within 12 months prior to the first dosing day.
  • The participant has participated in a clinical trial and has received an product within the following time period prior to dosing in the current study: 5 half-lives (if known) or twice the duration (if known) of the biological effect of the study intervention (whichever is longer) or 90 days (if half-life or duration is unknown), or, current participation in another clinical study
  • Enrollment into another clinical study whilst participating in this study.

Diagnostic assessments:

  • Positive pre-study drug/alcohol screen, including tetrahydrocannabinol (THC).
  • Cotinine levels indicative of regular or recent use of tobacco products or nicotine-containing products, including cigarettes, cigars, pipes and materials used to 'vape 'Positive (HIV) antibody test.

Liver safety:

  • (ALT) >1.5 × (ULN).
  • Total >1.5 × ULN (isolated total bilirubin >1.5 × ULN is acceptable if total bilirubin is fractionated and direct bilirubin \< 35 percent (%). Participants with Gilbert's syndrome can be included with total bilirubin >1.5xULN if direct bilirubin is \<= 1.5xULN.
  • For participants with benign unconjugated hyperbilirubinemia with total bilirubin >1.25 × ULN, the investigator should review the results in conjunction with other medical history to confirm eligibility.
  • Serum albumin \<=3.5 gram per deciliter (g/dL).
  • Presence of surface antigen (HBsAg) at screening or within 3 months prior to first dose of study intervention.
  • Positive antibody test result at screening or within 3 months prior to first dose of study intervention.

Note: Participants with positive hepatitis C antibody due to prior resolved disease can be enrolled, only if a confirmatory negative hepatitis C RNA test is obtained.

- Positive hepatitis C RNA test result at screening or within 3 months prior to first dose of study intervention.

Note: Test is optional and participants with negative hepatitis C antibody test are not required to also undergo hepatitis C RNA testing.

Cardiac Safety:

  • interval (QTc) QTcF >= 450 milliseconds (msec) (mean of triplicate measurements should be used at screening to confirm that participant meets exclusion criterion
  • Regular alcohol consumption within 6 months prior to the study defined as an average weekly intake of >14 units for males or females. One unit is equivalent to 8 g of alcohol: a half-pint (\~240 mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits.

Others:

  • Regular use of known drugs of abuse, including tetrahydrocannabinol (THC).
  • Sensitivity to heparin or heparin-induced thrombocytopenia.
  • Sensitivity or history of sensitivity to the study interventions, or components thereof, or drug or other allergy that, in the opinion of the investigator [or medical monitor] contraindicates participation in the clinical study.
  • Use of any products intended to treat medical conditions that are not approved by the governing health authority in a given country or region (for example, herbal medicine, health supplements, traditional medicine, homeopathic remedies, etc.).
  • Platelets \<140x10\^9/L.
Terms in these criteria, in plain language(19)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
98 participants (estimated)

Study arms

  • Experimental
    Group 1

    Bepirovirsen will be administered from a vial.

    Drug: Bepirovirsen

  • Experimental
    Group 2

    Bepirovirsen will be administered from an autoinjector.

    Drug: Bepirovirsen

Interventions

  • Bepirovirsen will be administered.

    Also known as: GSK3228836

06

What researchers measure

Primary outcomes

  1. Area Under the Concentration-time Curve from Time Zero (pre-dose) up to Day 8 [AUC(0- 8 d)] of Bepirovirsen in Plasma

    Time frame: Pre-dose to Day 8 (168 hours) post dose

  2. Maximum Observed Concentration (Cmax) of Bepirovirsen in plasma

    Time frame: Pre-dose to Day 8 (168 hours) post dose

Secondary outcomes

  1. Number of Participants with Adverse Events (AEs), Serious Adverse Events (SAEs), Treatment Related AEs Related SAEs

    Time frame: Up to 64 Days

  2. Number of Participants with Fatal SAEs, AEs of Grade 3 and above, and AEs Leading to Permanent Discontinuation of Study Intervention

    Time frame: Up to 64 Days

  3. Number of Participants with Adverse Event of Special Interest (AESIs)

    Time frame: Up to 64 Days

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Yes — Study Sponsor will assess requests from qualified researchers for anonymized individual patient-level data and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.gsk-studyregister.com/gsk-patient-level-data-sharing-july2025.pdf

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report

Time frame: Anonymized IPD will be made available within 6 months of publication of primary, key secondary and safety results for studies in product with approved indication(s) or asset(s) with development terminated across all indications.

Access criteria: Anonymized IPD is shared with researchers whose proposals are approved by an Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months, but an extension may be granted, when justified, for up to 6 months.

Data sharing details ↗ · www.gsk-studyregister.com

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Nov 2026; primary completion for Mar 2027, 4 months later.

Of 49 industry-sponsored phase 1 interventional studies under Hepatitis B, half reached primary completion within 13 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 24. This study's planned 4 months is below that.

Counting every sponsor, half of 58 studies reached it within 14 months; a quarter within 7 and three quarters within 27.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 23, 2026
First posted
Oct 29, 2026
StartEst.
Nov 3, 2026
Primary completionEst.
Mar 30, 2027
CompletionEst.
Mar 30, 2027
Last update
Oct 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07905157
Lead sponsor
GlaxoSmithKline
Responsible party
Sponsor
First posted
Oct 29, 2026
Start date
Nov 3, 2026 (estimated)
Primary completion
Mar 30, 2027 (estimated)
Completion
Mar 30, 2027 (estimated)
Last update
Oct 29, 2026

Study contacts

US GSK Clinical Trials Call Center
Contact
GSKClinicalSupportHD@gsk.com
877-379-3718
EU GSK Clinical Trials Call Center
Contact
GSKClinicalSupportHD@gsk.com
+44 (0) 20 89904466
GSK Clinical Trials
study director · GlaxoSmithKline

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Studies of the drug tested here: Bepirovirsen

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