MEDICI - t(11;14) and BCL2 Expression in Patients With Multiple Myeloma: Prevalence, Stability Across Lines of Therapy and Concordance Across Sample Types

Status: Completed
Location: See all (38) locations...
Study Type: Observational
SUMMARY

Multiple myeloma (MM) is a rare cancer caused by abnormal survival of plasma cells (blood cells). Most trial participants with MM relapse (cancer has come back) or become non- responsive to treatment and remission gets shorter after each line of treatment. This is a study to assess t(11;14) and BCL2 expression in adult participants with newly diagnosed and relapsed/refractory (R/R) MM. Approximately 500 adult participants with newly confirmed or relapsed/refractory (R/R) multiple myeloma (MM) will be enrolled in around 15-20 countries. Participants will receive standard of care while participating in this study. No drug will be administered as a part of this study. Participants will attend regular visits during the course of the study at a hospital or clinic and will be asked to provide bone marrow and blood samples.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• \- Confirmed newly diagnosed or relapsed/refractory (R/R) Multiple myeloma (MM) who have signed informed consent for the use of their biological material for research purposes.

Locations
United States
Louisiana
Tulane School of Medicine /ID# 223864
New Orleans
Texas
University of Texas Southwestern Medical Center /ID# 223865
Dallas
Other Locations
Argentina
Hospital Italiano de Buenos Aires /ID# 224153
Ciudad Autonoma Buenos Aires
Australia
Alfred Health /ID# 224386
Melbourne
Brazil
Hospital de Clinicas de Porto Alegre /ID# 224274
Porto Alegre
Instituto COI de Educacao e Pesquisa /ID# 224245
Rio De Janeiro
Hospital São Rafael /ID# 224307
Salvador
Clinica Sao Germano /ID# 224239
São Paulo
Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo /ID# 225749
São Paulo
Real e Benemérita Associação Portuguesa de Beneficência /ID# 224305
São Paulo
Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein /ID# 224303
São Paulo
Canada
Cross Cancer Institute /ID# 224172
Edmonton
Croatia
Klinicki bolnicki centar Zagreb /ID# 226969
Zagreb
France
CHRU Lille - Hopital Claude Huriez /ID# 228919
Lille
CHU de Nantes, Hotel Dieu -HME /ID# 223702
Nantes
AP-HP - Hopital Necker /ID# 228062
Paris
Germany
Praxis am Volkspark /ID# 224763
Berlin
Asklepios Klinik Altona /ID# 224761
Hamburg
Greece
Alexandra General Hospital /ID# 224828
Athens
Ireland
Beaumont Hospital /ID# 225514
Beaumont
Israel
Hadassah Medical Center-Hebrew University /ID# 224884
Jerusalem
Italy
Azienda Ospedaliero Universitaria Ospedali Riuniti di Ancona /ID# 224690
Ancona
ASST Grande Ospedale Metropolitano Niguarda /ID# 224608
Milan
Netherlands
Maastricht Universitair Medisch Centrum /ID# 224694
Maastricht
Norway
Rikshospitalet OUS HF /ID# 227288
Oslo
Poland
Szpital Kliniczny im. Heliodora Swiecickiego Uniwersytetu Medycznego im. Karola /ID# 227038
Poznan
Instytut Hematologii i Transfuzjologii /ID# 227039
Warsaw
Romania
Institutul Clinic Fundeni /ID# 224574
Bucharest
Saudi Arabia
Princess Noorah Oncology Center /ID# 224968
Jeddah
Slovenia
Univ Medical Ctr Ljubljana /ID# 225408
Ljubljana
Spain
Hospital Universitario Germans Trias i Pujol /ID# 229281
Badalona
Hospital Clinic de Barcelona /ID# 224804
Barcelona
Hospital de Leon /ID# 229191
León
Hospital Universitario 12 de Octubre /ID# 225617
Madrid
Hospital Universitario Fundacion Jimenez Diaz /ID# 229524
Madrid
Hospital Universitario de Salamanca /ID# 224803
Salamanca
Taiwan
Taichung Veterans General Hospital /ID# 227084
Taichung
Turkey
Bagcilar Medipol Mega Universite Hastanesi /ID# 225515
Istanbul
Time Frame
Start Date: 2021-07-07
Completion Date: 2023-09-30
Participants
Target number of participants: 514
Treatments
Participants With Multiple Myeloma
Participants with newly diagnosed and relapsed/refractory multiple myeloma will receive standard of care. Bone marrow and blood samples will be collected.
Related Therapeutic Areas
Sponsors
Leads: AbbVie

This content was sourced from clinicaltrials.gov