Clin2
NCT03058588Possibly a fitRecruiting

Genetic testing study for inherited AML or MDS risk

Leukemia

Part of Blood & lymphatic, Cancer clinical trials.

This study uses advanced DNA testing to look for inherited gene changes in people with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). It may help explain whether your illness could be part of a family-linked risk syndrome, which can guide treatment and family planning.

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

Phase
N/A
Enrollment
20 people
Ages
Any age
Study type
Observational

Who can take part

  • You have been diagnosed with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS)
  • A close family member (parent, sibling, child, or grandparent) has AML or MDS, or another myeloid blood cancer
  • OR a close family member has a lymphoma or other lymph “blood cancer”
  • OR you have personal signs that can fit certain inherited MDS/AML risk patterns (examples like easy bruising/low platelets, unusual nail/skin/oral changes, lung scarring with no clear cause, liver problems with no clear cause, swollen limbs, unusual infections, or immune problems)
  • You are able and willing to sign informed consent

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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