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Not yet recruitingNCT07917910Updated Nov 5, 2026

A Study of HT-101 and HT-102 in Chronic Hepatitis B (CHB)

A Phase 2 interventional study of HT-101 + HT-102 and HT-101 placebo + HT-102 placebo in Chronic Hepatitis B Virus Infection, sponsored by Suzhou HepaThera Biotech Co., Ltd.. Not yet recruiting. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-11-05.

Sponsored by Suzhou HepaThera Biotech Co., Ltd. · Phase 2, Interventional, and Treatment

Updated Nov 5, 2026Newly registeredGo to Updates ↓
Phase
Phase 2
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Phase II trial of HT-101 + HT-102 in CHB: (1) functional cure in treatment-naïve patients (vs placebo); (2) efficacy of sequential interferon in previously treated patients.

Read the detailed description

This is a Phase II clinical trial to evaluate the efficacy and safety of HT-101 Injection in combination with HT-102 Injection in participants with chronic hepatitis B virus infection. The primary objective is(1) to assess the efficacy of HT-101 Injection plus HT-102 Injection compared with placebo in achieving functional cure in treatment-naïve participants with chronic hepatitis B virus infection

02

Conditions studied

  • Chronic Hepatitis B Virus Infection

Browse trials for

03

In context

Hepatitis B, Chronic

895 studies on the registry are indexed under Hepatitis B, Chronic; 151 are open to participants now.

This study's planned enrollment of 120 is above the median of 100 across 659 interventional studies indexed under Hepatitis B, Chronic.

Browse Hepatitis B, Chronic studies →

Lead sponsor

Suzhou HepaThera Biotech Co., Ltd. is the lead sponsor of 5 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  1. Having a full understanding of the nature, significance, possible benefits, and risks of this study, demonstrating good compliance, and voluntarily signing the Form (ICF);
  2. Treatment-naïve participants clinically diagnosed with chronic virus (HBV) infection;
  3. Male or female participants of (WOCBP) must commit to having no plans for procreation, sperm or ovum donation during the study and for 6 months after the last dose, and must voluntarily use a highly effective method.

Exclusion criteria

Exclusion Criteria:

  1. Previous history of cirrhosis, or evidence suggesting significant hepatic fibrosis or cirrhosis;
  2. History of hepatocellular carcinoma (HCC) or suspected HCC;
  3. Individuals who have experienced major trauma or undergone major surgery within 3 months prior to screening, or who plan to undergo major surgery during the study period;
  4. Previous history of solid organ transplantation or hematopoietic stem cell transplantation ();
  5. Pregnant or lactating women, or those with a positive pregnancy test;
  6. Known allergy to any component of the product and/or other products of the same class, or history of severe food or drug allergy, or allergic constitution;
  7. Participants deemed by the investigator, for any other reason, to be unsuitable to participate in this study;
Terms in these criteria, in plain language(6)

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.

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.

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.

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.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

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.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    HT-101 + HT-102

    Drug: HT-101 + HT-102

  • Experimental
    HT-101 placebo + HT-102 placebo

    Drug: HT-101 placebo + HT-102 placebo

Interventions

  • DrugHT-101 + HT-102

    HT-101 given by subcutaneous injection.HT-102 given by subcutaneous injection.

  • DrugHT-101 placebo + HT-102 placebo

    HT-101 placebo + HT-102 placebo

06

What researchers measure

Primary outcomes

  1. Proportion of participants achieving functional cure at Week 24 of follow-up after discontinuation of all anti-hepatitis B medications.

    Time frame: Up to Week 72

07

Study locations

No study locations are listed for this record.

08

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 Oct 2026; primary completion for Oct 2028, 24 months later.

Of 75 industry-sponsored phase 2 interventional studies under Hepatitis B, Chronic, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 39. This study's planned 24 months is close to that.

Counting every sponsor, half of 87 studies reached it within 23 months; a quarter within 16 and three quarters within 41.

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

Registered
Oct 29, 2026
First posted
Nov 5, 2026
StartEst.
Oct 30, 2026
Primary completionEst.
Oct 30, 2028
CompletionEst.
Sep 17, 2029
Last update
Nov 5, 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
Nov 5, 2026
Show all 1 update
  1. Nov 5, 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 ↗

09

Registry details

Key details

Study ID
NCT07917910
Lead sponsor
Suzhou HepaThera Biotech Co., Ltd.
Responsible party
Sponsor
First posted
Nov 5, 2026
Start date
Oct 30, 2026 (estimated)
Primary completion
Oct 30, 2028 (estimated)
Completion
Sep 17, 2029 (estimated)
Last update
Nov 5, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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

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Discussion

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