Clin2
NCT07204392Possibly a fitRecruiting

Genetic study for early-onset or familial MPN

Myeloproliferative DiseaseGermline Mutation

Part of Blood & lymphatic clinical trials.

This study explores whether certain inherited gene changes make people more likely to develop myeloproliferative neoplasms (MPNs). It is looking at patients who were diagnosed at a young age or have a family history of blood cancers, to better understand the genetic causes of these conditions.

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

Phase
N/A
Enrollment
313 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You have a type of blood cancer called a myeloproliferative neoplasm (MPN). This includes Polycythemia Vera, Essential Thrombocythemia, or Primary Myelofibrosis.
  • You have already had a test to identify the main gene change (driver mutation) that caused your MPN.
  • Either you were diagnosed with MPN before turning 27 years old, OR you have at least one close relative (first or second degree) with a blood cancer.

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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