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NCT05710211
Clonal Architecture of ASXL1-mutated Myelofibrosis
Conditions: Myelofibrosis
Sex: All
Ages: 18 Years – N/A
Phase: NA
Enrollment: 50
Sponsor: University Hospital, Angers
Location: France
Summary
Prospective study to decipher the clonal architecture of ASXL1-mutated primary and secondary myelofibrosis and its impact on prognosis
Eligibility Criteria
Inclusion Criteria:Adults (age ≥18 years),Affiliated to the national social security system,ASXL1 mutated primary or secondary myelofibrosis,Signed the consent to participate in the study,Included, or consenting to be included, in the national clinical-biological database of France Intergroupe Syndrome Myéloprolifératifs (FIM).Exclusion Criteria:Patient with another active hematological disease or cancer at the time of diagnosis,Person subject to legal protection scheme or incapable of giving consent.
Source: ClinicalTrials.gov (NCT05710211). StuddyBuddy aggregates publicly available trial information.