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MYeloma Resistance And Clonal Evolution

MYeloma Resistance And Clonal Evolution

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03807128
Acronym
MYRACLE
Enrollment
1400
Registered
2019-01-16
Start date
2019-02-11
Completion date
2049-02-11
Last updated
2025-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Myeloma

Keywords

Myeloma, Cohort, Resistance, Quality of life

Brief summary

Multiple Myeloma (MM) is often associated with progression, temporary response to therapy and a high relapse rate over time resulting in a poor long-term prognosis. Because MM is classified as an incurable disease, therapeutic resistance is of great interest. However, knowledge about the biological mechanisms underlying resistance associated with MM therapies and about associated predictors remains poor. The MYRACLE cohort, a multicenter prospective cohort of patients with MM, is set up to address this limitation.

Detailed description

The MYRACLE cohort study aims at including all patients (\>18 years old) who are diagnosed with MM in any stage of the disease and treated in specialized oncology centers in 2 public hospitals in Northwestern France. Any such patient providing a signed informed consent is included. All subjects are followed up until refusal to participate in the study, emigration or death. The MYRACLE follow-up is continuous and collects data on socio-economic status, medical status, MM therapies and associated events (resistance, side effects). Participants also complete standardized quality of life (QOL) questionnaires. In addition, participants are asked to donate blood samples that will support ex vivo analysis of expression and functional assays required to uncover predictive biomarkers and companion diagnostics. If diagnostic biopsies are performed during the course of the disease, extracted biological samples are kept in a dedicated biobank.

Interventions

OTHERPrélèvement sanguin (2*4mL) ou médullaire (2mL)

Additional blood (2\*4mL) or bone marrow (2mL) sample depending on clinical presentation of disease

OTHERData collection through questionnaires

Collection of quality of life and occupational exposure data via questionnaires

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient consulting due to the discovery or recurrence of MM according to international diagnostic criteria (IMWG 2014) * Patient having consented to participate in the study and his/her biocollection * Patient affiliated to or benefiting from a social security scheme or similar

Exclusion criteria

* Minors * Major under guardianship or curatorship * Protected persons. * Pregnant or breast-feeding women * Persons benefiting from the AME

Design outcomes

Primary

MeasureTime frameDescription
Describe the mechanisms of resistance of myeloma cells.15 yearsNumber of resistance.

Countries

France

Contacts

Primary ContactCyrille TOUZEAU, PU
cyrille.touzeau@chu-nantes.fr02 40 08 32 71

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026