European Myeloma Network (EMN) Sample Project
About this study
This is an observational, non-interventional, multicenter study for the prospective collection, storage and analysis of patients' biological samples. This study establishes a common international infrastructure useful to collect standard clinical variables at baseline and during treatment and to uniformly collect and store biological samples
- Condition
- Multiple Myeloma, Smoldering Multiple Myeloma, Plasma Cell Leukemia, Extramedullary Myeloma, MGUS
- Tested
- storage of biological samples
- Sponsor
- European Myeloma Network B.V.
Who can join
- Age
- 18 years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
Inclusion 7
- Minimum age: 18 years
- Study condition: Multiple Myeloma, Smoldering Multiple Myeloma, Plasma Cell Leukemia, Extramedullary Myeloma, MGUS
- Subjects with MGUS, smouldering Multiple Myeloma (SMM) , MM (Multiple Myeloma) (+/- EMD), plasma cell leukemia (PCL) (+/- EMD)
- Subjects are ≥ 18 years old.
- Subjects have provided written informed consent in accordance with federal, local, and institutional guidelines prior to initiation of any project-specific activities or procedures.
- Subjects do not have kind of condition that, in the opinion of the Investigators, may compromise the ability of the subjects to give written informed consent and
- subjects are, in the investigator's opinion, willing and able to comply with the protocol requirements.
Exclusion 3
- Previous treatment with anti-myeloma therapy (excluding one course of therapy in patients in which urgent therapy is deemed necessary according to physician's discretion, e.g. myeloma-related complications resistant to supportive care).
- Subjects have had prior unforeseen (serious) adverse reactions to blood donation including, but not limited to fainting, angina, severe bruising, allergic reactions, or any other adverse events.
- Any psychological, familial, sociological and geographical condition potentially hampering compliance with the protocol and follow-up schedule.
Where
41 sites, 41 recruiting
Alfred Hospital
Melbourne, Australia
KUK Linz
Linz, Austria
Medical University Vienna
Vienna, Austria
Department of Haematology UZ Leuven Gasthuisberg
Leuven, Belgium
Nemocnice Havířov
Havířov, Czechia
Nemocnice Nový Jičín
Nový Jičín, Czechia
and 35 more sites on ClinicalTrials.gov
Contact
-
Chiara Del Pietro
+31 10702687065 chiara.delpietro@emn.org
Potential match only. Final eligibility is determined by the study team.