For Healthcare Professionals

realMIND: Observational Study on Safety and Effectiveness of Tafasitamab in Combination With Lenalidomide in Patients With Relapsed or Refractory DLBCL

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About the study

The realMIND study is a multicenter, observational study intended to further characterize the safety and effectiveness data of US patients (with a focus on racial and ethnic minority patients) with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL), treated with tafasitamab in combination with lenalidomide.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Criteria: Inclusion Criteria:

  1. Age ≥18 years at the time of diagnosis of R/R DLBCL
  2. Initiated or initiating tafasitamab treatment
  3. R/R DLBCL patients who have received at least one (1) prior line of treatment for DLBCL
  4. Histologically confirmed DLBCL such as:
  1. a) DLBCL not otherwise specified (NOS) b) T-cell histiocyte-rich large B-cell lymphoma (THRLBCL) c) Epstein-Barr virus (EBV)-positive DLBCL of the elderly d) Composite lymphoma with a DLBCL component with a subsequent DLBCL relapse, according to Revised European American Lymphoma (REAL)/World Health Organization (WHO) classification e) Patients with evidence of histological transformation to DLBCL from an earlier diagnosis of low-grade lymphoma (i.e., an indolent pathology such as follicular lymphoma [FL], marginal zone lymphoma [MZL], chronic lymphocytic leukemia [CLL]) with a subsequent DLBCL relapse f) High-grade B-cell lymphoma: i) DLBCL with MYC and BCL2 or BCL6 translocation (double-hit) and MYC and BCL2 and BCL6 translocations (triple-hit) ii) High-grade B-cell lymphoma, NOS
  2. Signed and dated ICF by the patient or the patient's Legally Acceptable Representative (LAR), for patients with prospective data collection, as applicable. For deceased or otherwise unreachable patients, no informed consent will be obtained for data collection in the study, provided that the competent Independent Ethics Committee (IEC)/Institutional Review Board (IRB) has provided favorable opinion and that any other local regulatory requirements on this matter are met

EXCLUSION CRITERIA

Exclusion Criteria:

• Initiated or initiating tafasitamab treatment in the context of an interventional study.

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 1.855.463.3463Email iconEmail Study Center

Study Details


Contition

Diffuse Large B-cell Lymphoma

Age

18+

Participants Needed

100

Est. Completion Date

Aug 31, 2026

Treatment Type

OBSERVATIONAL


Sponsor

Incyte Corporation

ClinicalTrials.gov NCT Identifier

NCT04981795

Study Number

MOR208C414

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