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RECRUITING
NCT05731245
PHASE2

Ropeginterferon Alfa 2b for Early MyelofibrosisDIPSS Low/Intermediate-1 Risk Myelofibrosis

Sponsor: National Taiwan University Hospital

View on ClinicalTrials.gov

Summary

This is a multi-centre phase 2 open-label prospective study designed to assess the efficacy and safety of ropeg patients with pre-fibrotic primary myelofibrosis or DIPSS low/intermediate-1 risk myelofibrosis after 24 months of treatment.

Official title: Efficacy and Safety of Ropeginterferon Alfa-2b for Pre-fibrotic Primary Myelofibrosis and DIPSS Low/Intermediate-1 Risk Myelofibrosis

Key Details

Gender

All

Age Range

20 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2023-02-08

Completion Date

2026-10-12

Last Updated

2023-02-16

Healthy Volunteers

No

Interventions

DRUG

Ropeginterferon Alfa-2B Prefilled Syringe [Besremi]

Eligible subjects will receive Ropeginterferon alfa-2b subcutaneously (SC) every 2 weeks at the starting dose of 250µg at week 0, 350 µg at week 2, then 500µg at a fixed dose from week 4 onwards

Locations (1)

National Taiwan University Hospital

Taipei, Taiwan, 100, Taiwan