RecruitingNCT06823960
Study to Assess Effectiveness and Safety of Zanubrutinib for Patients With Marginal Zone Lymphoma Treated in Italy Under the Named Patient Program (NPP)
An Italian Multicenter Retrospective Observational Study to Assess Effectiveness and Safety of Zanubrutinib for Patients With Marginal Zone Lymphoma Treated in Italy Under the Named Patient Program (NPP)
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Enrollment
59 participants
Start Date
Dec 9, 2024
Study Type
OBSERVATIONAL
Conditions
Summary
Observational, non-interventional, retrospective, multicentre study focusing on efficacy and safety of zanubrutinib in daily clinical practice in patients with relapsed/refractory (R/R) marginal zone lymphoma.
Eligibility
Min Age: 18 Years
Inclusion Criteria2
- Histologically confirmed diagnosis of relapsed/refractory marginal zone lymphoma
- Patients who received at least one dose of zanubrutinib under the Named patient program (D.M. 7 Sep 2017), between January 2021 and October 2023 3) Age≥18 at start of zanubrutinib therapy. 4) Signature of written informed consent to study participation and personal data processing.
Exclusion Criteria1
- \) relapsed/refractory marginal zone lymphoma patients who received zanubrutinib in a clinical trial context.
Locations(15)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06823960
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