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HBsAg Loss Adding Pegylated Interferon in HBeAg-negative Patients

J

José Antonio Carrion

Status

Completed

Conditions

Chronic Hepatitis B (HBeAg-negative)

Treatments

Drug: Pegylated interferon alfa-2a

Study type

Interventional

Funder types

Other

Identifiers

NCT02743182
QUANTI-B

Details and patient eligibility

About

Chronic hepatitis B (CHB) affects more than 350 million people worldwide. The most common form in Europe is CHB HBeAg-negative. Antiviral treatment of CHB HBeAg-negative patients includes chronic administration of nucleos(t)ide analogues (NUC) or pegylated interferon (PegIFN) during 12 months. Typically, PegIFN allows immune control of CHB and antigen "s" (HBsAg) loss in around 4% of patients compared to less than 0,1% using NUC. Recently, it has been described that HBsAg quantification (HBsAg-q) is useful to identify patients with high probability to lose HBsAg during follow-up. In addition, a proof-of-concept study with nine HBeAg-negative patients receiving NUC showed that adding PegIFN (16 weeks) achieved HBsAg loss in one patient (11%). The aim of our study is to evaluate the efficacy and safety adding PegIFN (48 weeks) in treated HBeAg-negative patients with NUC.

Enrollment

119 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic hepatitis B (HBeAg-negative)
  • Signed inform consent
  • Aged > 18

Exclusion criteria

  • Contraindications for Pegylated interferon (cirrhosis, pregnancy, others)
  • Previous treatment with interferon or Pegylated interferon
  • Previous HBsAg loss
  • Treatment duration with Nucleos(t)ide analogues less than 2 years
  • Poor adherence to Nucleos(t)ide analogues

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

119 participants in 2 patient groups

Pegylated interferon alfa-2a
Active Comparator group
Description:
adding Pegylated interferon alfa-2a (180 microgs /week during 48 weeks) in HBeAg-negative patients receiving nucleos(t)ide analogues
Treatment:
Drug: Pegylated interferon alfa-2a
Control
No Intervention group
Description:
HBeAg-negative patients receiving nucleos(t)ide analogues

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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