drugset / Trial / NCT01204762

Dose Ranging Study of Pegylated Interferon Lambda in Patients With Hepatitis B and Positive for the Hepatitis B e Antigen

NCT01204762 ↗

Phase 2 Completed 197 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

At least 1 dose of pegIFNλ will be identified which is safe, well tolerated, and efficacious for the treatment of chronic hepatitis B virus infection (CHB) Amendment 7, Part B Sub Study: The primary purpose of this amendment is to obtain preliminary data on the safety of pegylated interferon Lambda (Lambda) when administered in combination with Entecavir(ETV) to patients with hepatitis E antigen-positive (HBeAg-positive) chronic hepatitis B(CHB) infection employing a sequential therapy approach

Timeline

Start
2010-11
Primary completion
2013-12
Completion
2013-12

Outcome

Missed primary endpoint

paper however lambda non-inferiority was not met at week 24 post-treatment (13.8% vs. 30.1%, respectively; lambda vs. alfa 80% CI lower bound -24%). PMID 26739688 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Peginterferon Lambda-1a Protein / enzyme biologic 180 ug Subcutaneous
Comparator Peginterferon alfa-2a Protein / enzyme biologic 180 ug Subcutaneous
Background Entecavir Small molecule 0.5 mg Oral