Establishment of Genomic, Transcriptomic and Functional Characteristics of Tumor Cells in Hyperinflammatory Hemopathies
NCT04702932 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2021-01-11
Summary
Patients with monoclonal gammopathies either benign or malignant may develop inflammatory symptoms such as Schnitzler syndrome. We proposed to name those cases as monoclonal gammopathy of inflammatory significance, or MGIS.
The aim of the study is to search for inflammatory pathway that may be activated in case MGIS and to search if the genetic of tumoral cell could explain those activations.
Conditions
- Monoclonal Gammopathy of Undetermined Significance
- Multiple Myeloma
- Waldenstrom Macroglobulinemia
Sponsors & Collaborators
-
INSERM UMR 1163
collaborator UNKNOWN -
Assistance Publique - Hôpitaux de Paris
lead OTHER
Principal Investigators
-
Sophie GEORGIN-LAVIALLE, PU-PH · Assistance Publique - Hôpitaux de Paris
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-09-01
- Primary Completion
- 2026-09-01
- Completion
- 2036-09-01
Countries
- France
Study Locations
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