NCT06559033View on ClinicalTrials.gov

Determine the Frequency of Variants in the GBA/PSAP Genes in Patients With MM or MGUS

Not yet recruitingOBSERVATIONAL

Enrollment

300

Participants

Timeline

Start Date

June 1, 2025

Primary Completion Date

October 2, 2026

Study Completion Date

April 1, 2027

Conditions

Monoclonal Gammopathy of Undetermined SignificanceMyeloma Multiple

Interventions

BIOLOGICAL

Evaluation of the presence and number of mutated alleles of the GBA/PSAP genes in patients with MM or MGUS

Estimation of the frequency of variants in the PSAP/GBA genes in patients with MM or MGUS, then comparison with a reference frequency from databases such as the Exome Aggregation Consortium, the Exome Sequencing Project, the 1000 Genomes Project and the dbSNP.

All Listed Sponsors

lead

University Hospital, Rouen

OTHER

NCT06559033 - Determine the Frequency of Variants in the GBA/PSAP Genes in Patients With MM or MGUS | Biotech Hunter | Biotech Hunter