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Observational Retrospective Cohort Study of Systemic Therapies for R/R DLBCL

Completed
Conditions
Diffuse Large B Cell Lymphoma
Registration Number
NCT04697160
Lead Sponsor
MorphoSys AG
Brief Summary

To compare the efficacy outcomes of the L-MIND cohort with the effectiveness in a matched patient population treated with systemic NCCN/ESMO guideline listed regimens administered in routine clinical care.

Detailed Description

This retrospective observational cohort study aims to generate a historical control consisting of R/R DLBCL patients who received currently guideline recommended therapies.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3573
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Overall Survival (OS)through study completion, an average of 1 year
Secondary Outcome Measures
NameTimeMethod
Overall/Objective Response Rate (ORR)through study completion, an average of 1 year
Complete Response Rate (CR)through study completion, an average of 1 year
Duration of Response (DoR)through study completion, an average of 1 year
Time to next treatment (TTNT)through study completion, an average of 1 year
Progression Free Survival (PFS)through study completion, an average of 1 year
Treatment discontinuation rate due to adverse eventsthrough study completion, an average of 1 year
Duration of treatment exposurethrough study completion, an average of 1 year
Event Free Survival (EFS)through study completion, an average of 1 year

Trial Locations

Locations (1)

MorphoSys Research Site

🇬🇧

Westcliff-on-Sea, United Kingdom

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