About Waldenström macroglobulinemia
Waldenström macroglobulinemia is a rare disease catalogued by Orphanet (ORPHA:33226). It is associated with the MYD88 gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Waldenström macroglobulinemia trials.
Search ClinicalTrials.gov for "Waldenström macroglobulinemia" or filter by Orphanet code ORPHA:33226 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Waldenström macroglobulinemia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Waldenström macroglobulinemia. Updated daily.