- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07852091
A Novel Combination Therapeutic Strategy Aiming to Functional Cure for Chronic Hepatitis B Virus Infection (A)
Hepatitis B virus (HBV) infection is a major public health threat in China. At present, a functional cure, also known as clinical cure or sustained Hepatitis B surface antigen (HBsAg) loss, is recommended as the ideal endpoint of HBV treatment. However, HBsAg loss can be achieved in less than 10% of chronic hepatitis B (CHB) patients treated with current available antiviral drug interferonα (IFNα) or nucleos(t)ide analogues (NAs) monotherapy. With the support of the national major special funding for infectious diseases from "11th Five-Year Plan" to "13th Five-Year Plan", we have implemented a pioneer clinical study of sequential combination of IFNα therapy on NAs to treat NAs-treated CHB patients (ie. New Switch Study). This is the world's first clinical trial aiming to functional cure, which increased the rate of HBsAg loss to 15% in the overall population in our study, and to 30-50% among those with lower baseline HBsAg levels. How to further improve the HBsAg loss rate is an urgent issue for us. The key point of achieving functional cure is to reverse the HBV-specific T cell exhaustion and establish the long-term immune control against HBV infection. Programmed death-1(PD-1)/programmed death-ligand 1 (PD-L1) axis blockade has been demonstrated to reinvigorate exhausted CD8+ T cells, and would be a potential strategy to treat chronic HBV infection. In this study, a large multicenter prospective study will be performed to explore the safety and efficacy of a novel combination strategy involving immune checkpoint inhibitor (anti-PD-1/anti-PD-L1 antibody) and IFNα in CHB patients, observe the HBsAg loss rate in NA-treated CHB patients receiving this combination strategy, evaluate the potential of breaking immune tolerance by this strategy, and further assess its efficacy to further improve the clinical cure rate on the basis of New Switch Study. Based on New Switch Study, this study further attempts to reverse T cell exhaustion in CHB patients, explore a novel platform of combination therapy development for clinical cure, and ultimately increase the HBsAg loss rate to higher than 50% in overall patients. The implementation of the project is expected to reduce the burden of HBV infection in China and contribute to the goal of global elimination of hepatitis B and C by 2030 (WHO 2030).
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Fase 2
Contacten en locaties
Studiecontact
- Naam: Dachuan Cai, MD
- Telefoonnummer: +86 18323409779
- E-mail: cqmucdc@cqmu.edu.cn
Studie Contact Back-up
- Naam: Min Chen, PhD
- Telefoonnummer: +86 17338600343
- E-mail: mchen@hospital.cqmu.edu.cn
Studie Locaties
-
-
Chongqing Municipality
-
Chongqing, Chongqing Municipality, China, 400010
- Werving
- The 2nd affiliated Hospital of Chongqing Medical University
-
Hoofdonderzoeker:
- HONG REN, Professor
-
Contact:
- DACHUAN CAI
- Telefoonnummer: +8618323409779
- E-mail: cqmucdc@cqmu.edu.cn
-
Contact:
- HONG REN
- Telefoonnummer: +8613983888786
- E-mail: renhong0531@vip.sina.com
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Sign the informed consent form before inclusion and be able to complete the study according to the study requirements;
- 18-60 years old.
- NAs-naive/NAs-experienced CHB patients.
Exclusion Criteria:
- A history of allergy, or who are suspected by the researcher to be allergic to the active ingredient of the drug under study or its excipients;
- Use of inhibitors, inducers or substrates of CYP3A4 within 28 days before enrollment;
- Systematical use of immunosuppressants, immunomodulators (thymosin) and cytotoxic drugs within 6 months before enrollment, or vaccination of live attenuated vaccine within 1 month before enrollment;
- Acute infection within 2 weeks before enrollment which requires intravenous antibiotic treatment, or existing infection which requires anti-infection treatment when enrollment;
- Clinically significant acute and chronic liver disease not caused by HBV infection (judged by reseachers);
- Confirmed or suspected decompensated cirrhosis, including but not limited to: hepatic encephalopathy, hepatorenal syndrome, bleeding from esophageal varices, splenomegaly, ascites, etc, or evidence of progressive liver fibrosis;
- Primary liver cancer, or alpha-fetoprotein (AFP) is greater than 50 ug/L or imaging suggests the possibility of malignant liver lesions, or other malignant tumors or a history of other malignant tumors within 5 years before enrollment (except that the malignant tumors have been completely relieved after treatment and patients have not received additional medical or surgical intervention within 3 years before screening);
- A history of pathological fracture or osteoporosis;
- Gastrointestinal dysfunction or gastrointestinal diseases that might affect the absorption of oral drugs, such as severe gastric ulcer, erosive gastritis, partial gastrectomy, and persistent gastrointestinal symptoms (such as nausea, vomiting, or diarrhea) >2 grades;
- Serious diseases of circulatory, respiratory, urinary, blood, metabolic, immune, mental, neurological, renal and other systems;
- Major trauma or major surgery within 3 months before enrollment, or planned surgery during the study period;
- Blood donation/loss ≥ 400 mL within 3 months before enrollment, or given a blood transfusion within 3 months before enrollment, or blood donation/loss ≥ 200 mL within 1 month before enrollment;
- Platelet count<90 × 10^9/L, white blood cell count<3.0 × 10^9/L, neutrophil count<1.3 × 10^9/L, total serum bilirubin>2 × upper limit of normal (ULN), albumin<30 g/L, creatinine clearance ≤ 60 mL/min (calculated by CKD-EPI formula), or international normalized ratio of prothrombin time (INR)>1.5 (unless receiving stable anticoagulant therapy);
- Hepatitis C virus (HCV) antibody (+), HIV antigen/antibody (+), or treponema pallidum antibody (+) and rapid plasma regain (RPR) test (+);
- A history of continuous alcohol abuse within 3 years before enrollment (average daily alcohol consumption exceeds 20 gram);
- A history of drug dependence or drug abuse within 1 year before enrollment;
- Those who have participated in clinical trials of other investigational drugs or medical devices and taken investigational drugs or used medical devices within 3 months before enrollment;
- Female in suckling period or pregnancy test (+) during screening;
- Subjects who are considered by the researcher to have other factors that are not suitable for the study
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: NAs combined with Sintilimab/Envafolimab
NAs (Once/day, 1 capsule/time, oral)combined with Sintilimab(anti-PD-1 antibody, once/three weeks, dose lower than the dose used in cancer patients, intravenous injection) /Envafolimab(anti-PD-L1 antibody, once/two weeks, dose lower than the dose used in cancer patients, subcutaneous injection), followed by NAs monotherapy |
Sintilimab(anti-PD-1 antibody),once/three weeks, dose lower than the dose used in cancer patients, intravenous injection; Envafolimab(anti-PD-L1 antibody),once/two weeks, dose lower than the dose used in cancer patients, subcutaneous injection
Andere namen:
NAs(ETV/TDF/TAF), Once/day, 1 capsule/time, oral |
|
Actieve vergelijker: NAs
NAs(Once/day, 1 capsule/time, oral) |
NAs(ETV/TDF/TAF), Once/day, 1 capsule/time, oral |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Serum HBsAg
Tijdsspanne: Baseline
|
Serum HBsAg level |
Baseline
|
|
Serum HBsAg
Tijdsspanne: 24 weeks after the treatment
|
Serum HBsAg level |
24 weeks after the treatment
|
|
Serum HBsAg
Tijdsspanne: 48 weeks after the treatment
|
Serum HBsAg level |
48 weeks after the treatment
|
|
Serum HBsAg
Tijdsspanne: 24 weeks after the end of treatment
|
Serum HBsAg level |
24 weeks after the end of treatment
|
|
Serum HBV DNA
Tijdsspanne: Baseline
|
Serum HBV DNA level |
Baseline
|
|
Serum HBV DNA
Tijdsspanne: 24 weeks after the treatment
|
Serum HBV DNA level |
24 weeks after the treatment
|
|
Serum HBV DNA
Tijdsspanne: 48 weeks after the treatment
|
Serum HBV DNA level |
48 weeks after the treatment
|
|
Serum HBV DNA
Tijdsspanne: 24 weeks after the end of treatment
|
Serum HBV DNA level |
24 weeks after the end of treatment
|
|
Serum alanine aminotransferase (ALT)
Tijdsspanne: Baseline
|
Serum ALT level |
Baseline
|
|
Serum alanine aminotransferase (ALT)
Tijdsspanne: 24 weeks after the treatment
|
Serum ALT level |
24 weeks after the treatment
|
|
Serum alanine aminotransferase (ALT)
Tijdsspanne: 48 weeks after the treatment
|
Serum ALT level |
48 weeks after the treatment
|
|
Serum alanine aminotransferase (ALT)
Tijdsspanne: 24 weeks after the end of treatment
|
Serum ALT level |
24 weeks after the end of treatment
|
Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Tijdsspanne: Baseline
|
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb) |
Baseline
|
|
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Tijdsspanne: 24 weeks after the treatment
|
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb) |
24 weeks after the treatment
|
|
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Tijdsspanne: 48 weeks after the treatment
|
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb) |
48 weeks after the treatment
|
|
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Tijdsspanne: 24 weeks after the end of treatment
|
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb) |
24 weeks after the end of treatment
|
|
Immune response of T and B cells
Tijdsspanne: Baseline
|
Frequencies and functions of T and B cells (tested by flowcytometry/FluoroSpot/ELISPOT) |
Baseline
|
|
Immune response of T and B cells
Tijdsspanne: 24 weeks after the treatment
|
Frequencies and functions of T and B cells (tested by flowcytometry/FluoroSpot/ELISPOT) |
24 weeks after the treatment
|
|
Immune response of T and B cells
Tijdsspanne: 48 weeks after the treatment
|
Frequencies and functions of T and B cells (tested by flowcytometry/FluoroSpot/ELISPOT) |
48 weeks after the treatment
|
|
Immune response of T and B cells
Tijdsspanne: 24 weeks after the end of treatment
|
Frequencies and functions of T and B cells (tested by flowcytometry/FluoroSpot/ELISPOT) |
24 weeks after the end of treatment
|
|
Virus and host genome
Tijdsspanne: Baseline
|
Detect virus and host genome using peripheral blood and liver tissue by sequencing |
Baseline
|
|
Virus and host genome
Tijdsspanne: 24 weeks after the treatment
|
Detect virus and host genome using peripheral blood and liver tissue by sequencing |
24 weeks after the treatment
|
|
Virus and host genome
Tijdsspanne: 48 weeks after the treatment
|
Detect virus and host genome using peripheral blood and liver tissue by sequencing |
48 weeks after the treatment
|
|
Virus and host genome
Tijdsspanne: 24 weeks after the end of treatment
|
Detect virus and host genome using peripheral blood and liver tissue by sequencing |
24 weeks after the end of treatment
|
Medewerkers en onderzoekers
Medewerkers
Onderzoekers
- Studie directeur: Hong Ren, MM, The Second Affiliated Hospital of Chongqing Medical University
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Door bloed overgedragen infecties
- Pathologische processen
- Chronische ziekte
- Ziekte attributen
- Infecties
- Virusziekten
- Ziekten van het spijsverteringsstelsel
- Lever Ziekten
- Hepatitis, viraal, menselijk
- Overdraagbare ziekten
- DNA-virusinfecties
- Hepadnaviridae-infecties
- Hepatitis, chronisch
- Hepatitis
- Pathologische aandoeningen, tekenen en symptomen
- Hepatitis B
- Hepatitis B, chronisch
- Envafolimab
- Sintilimab
Andere studie-ID-nummers
- 2025-0215
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .