drugset / Trial / NCT05222555

Safety and Pharmacokinetics Study of a Modified Tafasitamab IV Dosing Regimen Combined With Lenalidomide in R-R DLBCL Patients

NCT05222555

Phase 1/2 Active not recruiting 53 enrolled Incyte Corporation
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicentre study too Evaluate the Safety and Pharmacokinetics of a Modified Tafasitamab IV Dosing Regimen Combined with Lenalidomide (LEN) in Patients with Relapsed or Refractory Diffuse Large B-Cell Lymphoma (R/R DLBCL) who have had at least one, but no more than three prior systemic regimens and who are not eligible for high dose chemotherapy (HDC) with autologous stem-cell transplantation (ASCT) at the time of study entry.

Timeline

Start
2022-07-19
Primary completion
2024-07-17
Completion
2027-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Tafasitamab Monoclonal antibody Intravenous
Background Lenalidomide Other / unclassified Oral