Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Determine the Frequency of Variants in the GBA/PSAP Genes in Patients With MM or MGUSBlood Protein Disorders, Hemic and Lymphatic Diseases, Hypergammaglobulinemia, Neoplasms by Histologic Type, cardiovascular disorder, hematologic disorder, hemorrhagic disease, immune system disorder, immunoproliferative disorder, lymphoproliferative syndrome, monoclonal gammopathy, monoclonal gammopathy of uncertain significance, neoplasm, plasma cell myeloma, plasma cell neoplasm, vascular disorder, vascular hemostatic diseaseRecruitingNot stated2026-06-10NCT06559033

1 results · Page 1 of 1

Swipe the table sideways for more columns.

OrganizationsLinked trials
University Hospital, Rouen141

2 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
Centre Henri BecquerelRouenFrance10
University Rouen HospitalRouenFrance9