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Safety and Antiviral Activity of a Monoclonal Hepatitis B Antibody: a Phase 1b, Open-label Trial in Individuals With Chronic Hepatitis D Infection

27 maggio 2026 aggiornato da: Ole Schmeltz Søgaard, Aarhus University Hospital

Safety and Antiviral Activity of a Monoclonal Hepatitis B Antibody: a Phase 1b, Open-label Trial in Individuals With Chronic Hepatitis D Infection (the SAMBA-D Study)

Hepatitis D virus (HDV) is a major global health issue, with an estimated 12 million people living with the infection worldwide. HDV infection requires the presence of hepatitis B virus (HBV), as it relies on hepatitis B virus for replication within the liver cells. Treatment options for HDV are limited and cannot cure the infection. The combination of concurrent HBV and HDV increases the risk of developing severe liver disease, including cirrhosis and liver cancer. This risk would significantly decrease if HDV is eliminated or reduced. Consequently, there is a need for the development of new treatment options.

Colleagues at Rockefeller University in New York have identified the antibody HepB mAb19, which effectively reduces the amount of circulating HBV antigens. Since HDV depends on HBV to replicate, we will test this antibody as a potential treatment for HDV.

The trial design is a phase 1b open-label aiming at including 15 study participants with chronic hepatitis D infection. All study participants will receive two or three dosis of the antibody, HepB mAB19, and will be followed for 60 weeks after the first HepB mAb19 infusion.

This study will evaluate the safety and pharmacokinetics of this antibody, as well as its potential effects on viral levels of HDV RNA and antiviral immune responses in individuals living with chronic HDV infection.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

15

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Ole Schmeltz Søgaard, MD, PhD, professor
  • Numero di telefono: +45 24 77 79 95
  • Email: olesoega@rm.dk

Backup dei contatti dello studio

  • Nome: Henriette Vendelbo Graversen, MD
  • Numero di telefono: +45 51 49 25 95
  • Email: henrgv@rm.dk

Luoghi di studio

      • Aarhus, Danimarca, 8000
        • Reclutamento
        • Aarhus University Hospital
        • Contatto:
          • Henriette Vendelbo Graversen, MD
          • Numero di telefono: +45 51 49 25 95
          • Email: henrgv@rm.dk
      • Berlin, Germania
        • Non ancora reclutamento
        • Charité - Universitätsmedizin Berlin
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • HDV infection confirmed by positive anti-HDV antibody and detectable HDV RNA
  • HBs antibody negative during screening period
  • Both HBeAg positive and negative participants are included
  • Ability and willingness to provide informed consent
  • Participants who can become pregnant must agree to use two methods of contraception:
  • Participants who can impregnate a partner and who are engaging in sexual activity that could lead to pregnancy must agree to use condoms 10 days prior to study entry and during study follow up to avoid impregnating a partner who can get pregnant.

Exclusion Criteria:

  • Child-Turcotte-Pugh >9 points
  • Severe clinical hepatic decompensation-such as hepatic encephalopathy or variceal hemorrhage-occurring currently or within the past 12 months.
  • Any confirmed significant allergic reactions (urticaria or anaphylaxis) against monoclonal antibody or vaccine, or multiple drug allergies (non-active hay fever is acceptable)
  • Pregnancy or lactation
  • Any vaccination 2 weeks prior to entry
  • Prior receipt of HepB mAb19 therapy
  • Any significant acute infection (e.g. influenza, COVID-19) or any other clinically significant illness 2 weeks prior to entry
  • Active hepatitis C infection
  • Untreated HIV disease
  • Individuals with HIV receiving antiretroviral therapy who have had a measurement of plasma HIV RNA (viral load) >50 copies/mL within the past 6 months are excluded. However, a single viral load measurement between >50 and <500 copies/mL during this period is acceptable.
  • Participation in another clinical study of an investigational product currently or 12 weeks prior to entry, or expected participation during this study

Laboratory abnormalities in the parameters listed below:

  • Alpha fetoprotein >100 ng/mL
  • Hemoglobin <10 gm/dL (6.21 mmol/L)
  • Platelet count <25,000 /mm3
  • Estimated glomerular filtration rate (eGFR) <60 mL/min
  • ALT ≥ x10 upper limit of normal (ULN)

Current, or history of:

  • Clinical cardiovascular disease (e.g., cardiac insufficiency, coronary artery disease, cardiomyopathy, congestive heart failure.
  • Presence of clinically significant ECG abnormalities based on the average of the triplicate ECG recordings (e.g., PR interval >210 ms (1st degree AV block only if clinical symptoms are present), QT corrected for heart rate using the Fridericia's correction factor [QTcF] > 450 ms for males and QTcF >470 ms for females);
  • Chronic liver disease from another cause, ICD, or autoimmune diseases that in the opinion of the investigator would preclude participation
  • History of hematopoietic stem cell transplant or solid organ transplant

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Opel label
All participants will be included in this study arm
All participants will receive a dose of HepB mAb19 at day 0 of 10 mg/kg and at day 28 of 30 mg/kg. They will receive a third dose at day 140 of 30 mg/kg if we observe a 1-log decrease in HDV RNA from week 0 to week 6.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Safety and tolerability
Lasso di tempo: Two weeks after each administration
Rate and severity of solicited adverse events that are Grade 2 or above
Two weeks after each administration
Safety and tolerability
Lasso di tempo: 2, 12, 28 and 60 weeks after first HepB mAb19 administration
Rate and severity of treatment-emerging unsolicited adverse events (including confirmed laboratory abnormalities) 2, 12, 28 and 60 weeks after first HepB mAb19 administration.
2, 12, 28 and 60 weeks after first HepB mAb19 administration
Safety and tolerability
Lasso di tempo: From enrollment to end of follow-up at week 60
Rate and severity of serious adverse events (SAEs) throughout the study period following investigational product (IP) administration
From enrollment to end of follow-up at week 60
Safety and tolerability
Lasso di tempo: From enrollment to end of follow-up at week 60
Rate and severity of adverse events of special interest, such as immune complex disease (ICD) throughout the study period following IP administration.
From enrollment to end of follow-up at week 60
Pharmacokinetic profile
Lasso di tempo: From enrollment to end of follow-up at week 60
HepB mAb19 levels in serum will be measured by a validated sandwich ELISA method developed and performed by Celldex Therapeutics. HepB mAb19 levels will be measured before and at the end of each of the antibody administrations, at 3 and 6 hours, and at later time points during follow up.
From enrollment to end of follow-up at week 60
Pharmacokinetic profile
Lasso di tempo: From enrollment to end of follow-up at week 60
Assesment of HepB mAb19 elimination half-life (t1/2)
From enrollment to end of follow-up at week 60
Pharmacokinetic profile
Lasso di tempo: From enrollment to end of follow-up at week 60
Assesment of clearance (CL/F) of HepB mAb19
From enrollment to end of follow-up at week 60
Pharmacokinetic profile
Lasso di tempo: From enrollment to end of follow-up at week 60
Calculation of volume of distribution (Vz/F)
From enrollment to end of follow-up at week 60
Pharmacokinetic profile
Lasso di tempo: From enrollment to end of follow-up at week 60
Calculation of area under the curve (AUC) for HepB mAb19
From enrollment to end of follow-up at week 60
Pharmacokinetic profile
Lasso di tempo: From enrollment to end of follow-up at week 60
Calculation of HepB mAb19 decay curve
From enrollment to end of follow-up at week 60

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Virologic response
Lasso di tempo: From baseline (day 0) to week 28
Virologic response defined as HDV RNA decrease of ≥2 log10 IU/mL or to undetectable from baseline (day 0) to week 28.
From baseline (day 0) to week 28
Anti-drug antibodies
Lasso di tempo: From enrollment to end of follow-up at week 60
Rate of induced anti-HepB mAb19 antibodies.
From enrollment to end of follow-up at week 60
Changes in liver function tests
Lasso di tempo: From enrollment to end of follow-up at week 60
Changes in liver function tests (e.g. ALT, AST, alkaline phosphatase, bilirubin, albumin) at selected follow-up visits.
From enrollment to end of follow-up at week 60

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
HBV markers
Lasso di tempo: From enrollment to end of follow-up at week 60
  • Change in quantitative serum HBsAg levels from baseline (day 0) and from achieved nadir (lowest serum HBsAg level following IP administration) at each scheduled follow up visit.
  • HBV DNA levels at baseline and selected follow up visits
  • HBcrAg levels at baseline and selected follow up visits.
  • HBsAb conversion from negative at baseline to positive at selected follow up visits.
  • HBeAg levels at baseline and selected follow up visits.
  • HBeAb conversion from negative at baseline to positive at selected follow up visits, among participants who are seronegative at baseline.
  • HBV-specific T and B cell immune responses following HepB mAb19 administration.
From enrollment to end of follow-up at week 60
HDV markers
Lasso di tempo: From enrollment to end of follow-up at week 60
- Anti-HDV at baseline and at selected follow-up visits.
From enrollment to end of follow-up at week 60
Innate immune response
Lasso di tempo: From enrollment to end of study at week 60
Changes in innate immune responses following HepB mAb19 administration.
From enrollment to end of study at week 60
Changes in inflammatory markers
Lasso di tempo: From enrollment to end of follow-up at week 60
Changes in inflammatory markers following HepB mAb19 administration.
From enrollment to end of follow-up at week 60
Changes in fibrosis grade
Lasso di tempo: From enrollment to end of follow-up at week 60.
Changes in fibrosis grade by FibroScan from entry to end of study.
From enrollment to end of follow-up at week 60.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Collaboratori

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

23 aprile 2026

Completamento primario (Stimato)

1 aprile 2028

Completamento dello studio (Stimato)

1 aprile 2028

Date di iscrizione allo studio

Primo inviato

12 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

27 maggio 2026

Primo Inserito (Effettivo)

28 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

28 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • SAMBA-D-001
  • 2025-522125-36-00 (Ctis)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .