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NCT02853214: PreFamDys
Familial Dysglobulinemia
NA trial testing Genetic analysis of peripheral blood samples in Dysglobulinemia in 1,868 participants. Completed in 25 September 2023.
25 September 2023
Quick facts
| Lead sponsor | Hospices Civils de Lyon |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | screening |
| Enrollment | 1,868 |
| Start date | 6 February 2008 |
| Primary completion | 25 September 2023 |
| Estimated completion | 25 September 2023 |
| Sites | 47 locations across France |
Drugs / interventions tested
- Genetic analysis of peripheral blood samples
Conditions studied
- Dysglobulinemia — all drugs for Dysglobulinemia →
Sponsor
Hospices Civils de Lyon — full company profile →
Who can join
18 and older, any sex, with Dysglobulinemia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Multiple Myeloma (MM) is a malignant proliferation of monoclonal plasma cells. Myeloma accounts for almost 14% of all hematologic cancers and is essentially incurable. Myeloma commonly evolves from a precursor disease, Monoclonal gammopathy of undetermined significance (MGUS). Despite intensive study, the etiology of MGUS and myeloma are unknown and no lifestyle or environmental exposure factors have been identified that are consistently linked to increased risk of MM, MGUS or the transition between the two. The overall goal is to identify risk genes for dysglobulinemia, and more specifically Multiple Myeloma. This will involve the conservation of cells in a bank and genetic sequencing on samples obtained from families with at least two cases of dysglobulinemia. Material used for sequencing is likely to include fresh peripheral blood cells or lymphoblastoid lines established from peripheral blood lymphocytes of patients.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Clinical characteristics and outcome of 318 families with familial monoclonal gammopathy: A multicenter Intergroupe Francophone du Myélome study.
Dumontet C, Demangel D, Galia P, Karlin L, et al · · 2023 · cited 5× · PMID 36588407 · DOI 10.1002/ajh.26785
Verify or expand the search:
- PubMed search for NCT02853214
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02853214 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hospices Civils de Lyon
- Last refreshed: 3 September 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02853214.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing