Marginal Zone Lymphoma (MZL) Clinical Trials

Find Marginal Zone Lymphoma (MZL) Clinical Trials Near You

Integrated Molecular and Clinical Profiling of Transformed Splenic Marginal Zone Lymphoma

Status: Recruiting
Location: See all (7) locations...
Study Type: Observational
SUMMARY

Histological transformation in Splenic Marginal Zone Lymphoma (t-SMZL) represents an unmet clinical and biological need, invariably associated with poor prognosis and reduced overall survival. At the present time, there are no recommended treatments intended specifically to t-SMZL and little is known about t-SMZL genetic complexity. The aim of this study is to provide information that will help clinicians to better understand the complexity of the disease. The information gained from this study will also lead to more specific and effective treatment for patients with t-SMZL.

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

• Adults aged 18 years or older, regardless of the gender;

• Diagnosis of HT of SMZL (both at baseline, co-occurring with diagnosis of SMZL, or during the natural history of the disease);

• Availability of diagnostic tumor material (either frozen or FFPE) from spleen, lymph node, extra nodal site, peripheral blood or bone marrow collected at the time of histological transformation. Tumor material (either frozen or FFPE), from spleen, peripheral blood or bone marrow, collected at the time of SMZL diagnosis will be also collected, if available;

• Availability of the baseline and follow-up annotations.

Locations
United States
New York
Columbia University
NOT_YET_RECRUITING
New York
Other Locations
Belgium
Universitz Hospitals Leuven
NOT_YET_RECRUITING
Leuven
France
Hôpital Saint Louis
RECRUITING
Paris
Italy
Fondazione IRCCS Policlinico San Matteo
RECRUITING
Pavia
Spain
Hospital Clínic de Barcelona
RECRUITING
Barcelona
Switzerland
Oncology Institute of Southern Switzerland
NOT_YET_RECRUITING
Bellinzona
United Kingdom
University Hospitals Dorset
NOT_YET_RECRUITING
Bournemouth
Contact Information
Primary
IELSG Study Coordination Office
ielsg@ior.usi.ch
+41 58 666 7321
Backup
Davide Rossi, MD
davide.rossi@eoc.ch
+41 91 811 8540
Time Frame
Start Date: 2025-10-13
Estimated Completion Date: 2029-03
Participants
Target number of participants: 100
Related Therapeutic Areas
Sponsors
Leads: International Extranodal Lymphoma Study Group (IELSG)

This content was sourced from clinicaltrials.gov