About this trial
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 interferon (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).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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.
Disqualifiers
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;
Trial design
Parallel
Treatments tested in this trial
anti-PD-1/anti-PD-L1 antibody
DrugOnce/two or three weeks, dose lower than the dose used in cancer patients, subcutaneous/intravenous injection
NAs
DrugOnce/day, 1 capsule/time, oral
PEG-IFNα
DrugOnce/week, 180μg/time, subcutaneous injection
Treatment groups
Trial outcomes
Primary outcomes
Serum HBsAg
Serum HBsAg level
Serum HBsAg
Serum HBsAg level
Serum HBsAg
Serum HBsAg level
Serum HBsAg
Serum HBsAg level
Other outcomes
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Levels of other HBV markers (HBsAb, HBeAg, HBeAb, and HBcAb)
Sponsors and contacts
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The Second Affiliated Hospital of Chongqing Medical University
Lead sponsor
The Affiliated Hospital Of Southwest Medical University
Collaborator
Guizhou Provincial People's Hospital
Collaborator
Chongqing Three Gorges Central Hospital
Collaborator
First Affiliated Hospital of Chongqing Medical University
Collaborator