OncRef

Clinical Trial: NCT04134936

Phase Ib Study to Assess Safety and Preliminary Efficacy of Tafasitamab or Tafasitamab Plus Lenalidomide in Addition to R-CHOP in Patients With Newly Diagnosed DLBCL

Status:

COMPLETED

Phase:

Phase 1

Lead Sponsor:MorphoSys AG
Information Provided By:MorphoSys AG
Last Update Posted:2024-10-16

Study Overview

Brief Summary

This is an open-label, randomized, multicentre study to evaluate safety and preliminary efficacy of the human anti-CD19 antibody Tafasitamab in addition to R-CHOP (Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, Prednisone) or Tafasitamab and Lenalidomide in addition to R-CHOP in adult patients with newly diagnosed, previously untreated Diffuse Large B-cell Lymphoma (DLBCL).

Official Title

A Phase Ib, Open-label, Randomized Study to Assess Safety and Preliminary Efficacy of Tafasitamab in Addition to R-CHOP or Tafasitamab Plus Lenalidomide in Addition to R-CHOP in Patients With Newly Diagnosed Diffuse Large B-Cell Lymphoma (DLBCL) - First-MIND

Conditions

Diffuse Large B-cell Lymphoma

Intervention / Treatment

  • Drug: Tafasitamab
  • Drug: Tafasitamab plus lenalidomide

Other Study ID Numbers

  • MOR208C107

Start Date (Actual)

2019-12-11

Primary Completion Date (Actual)

2021-02-11

Study Completion Date (Actual)

2022-08-10

Enrollment (Actual)

66

Study Type

Interventional

Phase

Phase 1