drugset / Trial / NCT03003325

The Benefit/Risk Profile of AOP2014 in Low-risk Patients With PV

NCT03003325 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The Low-PV study is a multicenter, phase II, randomized trial aimed to assess whether the addition of Pegylated Proline-interferon-alpha-2b to the best therapeutic current strategy available based on phlebotomies and low dose acetylsalicylic acid (ASA) could improve the efficacy of treatment of patients with PV at low risk of thrombosis (younger than 60 years and without prior vascular events), in term of control of recommended level of hematocrit \< 45%, over a period of 12 months.

Timeline

Start
2017-02-02
Primary completion
2022-03-31
Completion
2023-03-31

Outcome

Met primary endpoint

paper The primary end point was met in 81% and 51% in the ropeg and standard groups, respectively. PMID 38320126 ↗

paper In this 24-month trial, ropeg was superior to phlebotomy alone in maintaining hematocrit on target. PMID 38320126 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ropeginterferon alfa-2b Protein / enzyme biologic 100 ug Subcutaneous
Background ASA Unknown 100 mg —