drugset / Trial / NCT05467553

A Study to Compare P1101 Plus TAF With or Without UDCA in Patients With HBV and HDV Co-Infection

NCT05467553

RandomizedParallel-groupOpen-labelTreatment

Summary

This is an open-label, randomized, multi-center study in patients with chronic HBV and HDV co-infection.

Timeline

Start
2023-02-24
Primary completion
2025-02-28
Completion
2025-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropeginterferon alfa-2b Protein / enzyme biologic 450 ug Subcutaneous
Subject Ursodeoxycholic Acid Small molecule 15 mg/kg
Background tenofovir alafenamide Small molecule 25 mg Oral