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Study to Evaluate the Safety and Efficacy of Tafasitamab Plus Lenalidomide in Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma (firmMIND)
MinorPrimary completion date changed from estimate of Apr 1, 2026 to Mar 30, 2026v33
Minor2 versionsRe-verified since Jul 3, 2025, no change to tracked fieldsv31-v32
MinorTrial status: Recruiting to Active, Not RecruitingEnrollment target: estimated 81 to confirmed 82 · Primary completion date: Dec 24, 2025 to Apr 1, 2026 · Completion date: Dec 24, 2026 to Apr 1, 2027 · 1 morev30Show 4 more changesShow less
Enrollment target: estimated 81 to confirmed 82
Primary completion date: Dec 24, 2025 to Apr 1, 2026
NotablePrimary completion date: Dec 24, 2026 to Dec 24, 2025Start date changed from estimate of Nov 16, 2022 to Dec 23, 2022 · Site details revised at 10 of 58 sitesv6Show 2 more changesShow less
Start date changed from estimate of Nov 16, 2022 to Dec 23, 2022
Site details revised at 10 of 58 sites
MinorStudy sites: 57 to 58v5
MinorStudy sites: 56 to 57v4
NotableTrial status: Not Yet Recruiting to RecruitingPrimary and study completion dates: Apr 17, 2026 to Dec 24, 2026 · Start date: Oct 15, 2022 to Nov 16, 2022 · Study sites: 0 to 56v3Show 3 more changesShow less
Primary and study completion dates: Apr 17, 2026 to Dec 24, 2026
Start date: Oct 15, 2022 to Nov 16, 2022
Study sites: 0 to 56
NotableStart date: Aug 24, 2022 to Oct 15, 2022Primary and study completion dates: Dec 16, 2026 to Apr 17, 2026v2Show 1 more changeShow less
Primary and study completion dates: Dec 16, 2026 to Apr 17, 2026
MinorStudy First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to assess the efficacy and safety of of tafasitamab plus lenalidomide in adults with diffuse large B-cell lymphoma (DLBCL) who have relapsed or are refractory to at least 1 but no more than 3 previous systemic DLBCL treatment regimens and who are not eligible for high-dose chemotherapy (HDC) and autologous stem cell transplantation (ASCT).