ANRS HB07 IP-Cure-B
ANRS HB07 IP-Cure-B proof of concept (PoC) clinical trial. Educating the liver immune environment through TLR8 stimulation followed by NUC discontinuation
Topic
Chronic hepatitis B
Sponsor
Inserm – ANRS
Coordinating investigator
Fabien Zoulim MD, PhD – Hospices Civils de Lyon
Short description
Chronic hepatitis B (CHB) is a major public health care issue worldwide and one of the principal causes of chronic liver disease, cirrhosis and hepatocellular carcinoma (HCC). Liver cancer is the third leading cause of cancer deaths globally, with the highest burden of disease found in regions where HBV is endemic.
New treatment options that enhance rates of HBsAg clearance with or without seroconversion are needed. Such treatments will allow patients to discontinue life-long oral antiviral therapy and provide an option for a functional cure with a finite duration of treatment.
The ANRS HB07 IP-cure-B study is a proof of concept Phase II clinical trial in HBeAg negative virally suppressed non-cirrhotic CHB patients. It will explore whether stopping NUC or stopping NUC after SLGN administration can increase the rate of HBsAg decline compared to standard of care CHB treatment. Exploratory analyses will help elucidate whether modifications in the liver immune environment are responsible for HBsAg decline.
Study design
Phase II, randomized, multicenter, open-label, exploratory study to examine in virally suppressed, non-cirrhotic HBeAg-negative CHB patients whether stopping NUC or stopping NUC after SLGN administration can increase the rate of HBsAg decline compared to standard of care CHB treatment
Primary objective
To study the virological efficacy, defined as ≥ 1 log10 IU/mL decline in HBsAg at 76 weeks, of both stopping NUC and stopping NUC after SLGN treatment compared to a control arm (NUC taken continuously for 76 weeks) which is defined as the standard of care for CHB treatment in HBeAg negative patients.
Primary endpoint
Percentage of subjects with ≥ 1.0 log10 IU/mL decline of HBsAg at week 76 compared to baseline
Study population
CHB virally suppressed patients
Intervention
20 participants will receive pre-study NUC for 76 weeks (arm A), 40 participants will receive pre-study NUC for 28 weeks (arm B) and 40 participants will receive pre-study NUC plus Selgantolimod for 28 weeks (arm C)
Number of subjects
100 participants
Participating country(ies) and sites
8 highly qualified Liver centres in 4 European countries: France (Lyon, Marseille, Nantes (x2), Paris), Germany (Freiburg), Italy (Milan, Parma) and Spain (Barcelona)
Study duration
41 months
Funding
The IP-Cure-B project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement n°847939
UMS MART/EUCLID activities
Methodological aspects, trial coordination, data management, statistical analysis, monitoring coordination