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Adding Ropeginterferon to Ruxolitinib for Myelofibrosis

Myelofibrosis

Treatments studied

Part of Blood & lymphatic clinical trials.

This study tests whether adding a type of interferon (ropeginterferon) to your current myelofibrosis treatment (ruxolitinib) is safe and tolerable. Myelofibrosis is a blood disorder where bone marrow becomes scarred; this combination might help control the disease better.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
15 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have primary myelofibrosis, post-polycythemia vera myelofibrosis, or post-essential thrombocythemia myelofibrosis with specific genetic mutations (JAK2, CALR, or MPL)
  • You have been on a stable dose of ruxolitinib for at least 6 weeks before joining the trial
  • Your spleen is enlarged (larger than 450ml) confirmed by imaging
  • Your blood tests show adequate kidney, liver, and blood cell function
  • You are at least 18 years old and able to give informed consent
  • If you can become pregnant, you must use reliable contraception and cannot be pregnant at the start

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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