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A Real-world Study of Tafasitamab in Combination With Lenalidomide in Patients withR/R DLBCL

Z

Zhao Weili

Status

Not yet enrolling

Conditions

Diffuse Large B-cell Lymphoma

Treatments

Drug: Tafasitamab Injection

Study type

Observational

Funder types

Other

Identifiers

NCT05883709
KY2023-006

Details and patient eligibility

About

To evaluate the real-world efficacy of Tafasitamab combined with Lenalidomide base regimen in patients with relapsed or refractory DLBCL, with objective response rate as the primary end point.

Full description

This study retrospectively collected the data of patients previously treated with Tafa and divided them into two coords according to different protocols received. Cohort 1 was Tafa combined treatment group, which could include Tafa combined with lenalidomide, Tafa combined with Lenalidomide plus BTK inhibitor, Tafa combined with Lenalidomide plus chemotherapy (including ADC). Cohort 2 was treated with sequential CAR T or graft after Tafa combination therapy.

Enrollment

15 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with pathological diagnosis of DLBCL, including but not limited to non-specific DLBCL (NOS-DLBCL); Large B-cell lymphoma (THRLBCL) rich in T cells/histiocytes; EBV positive DLBCL (EBV-positive DLBCL); According to the revised REAL/WHO classification, it was grade 3b follicular lymphoma, including DLBCL component, followed by DLBCL recurrence. In addition, patients with low-grade lymphomas such as follicular lymphoma, marginal zone lymphoma, and chronic lymphocytic leukemia have histological evidence of transformation to DLBCL and subsequent recurrence
  • Patients who, as determined by the treating physician, would benefit from Tafa treatment

Exclusion criteria

  • Known allergy or metabolic disorder to any drug in the regimen
  • Those who refuse to use reliable methods of contraception during pregnancy, lactation or age-appropriate period
  • Have a history of uncontrolled medical disease (including uncontrolled diabetes, severe heart, lung, liver, renal insufficiency), blood, endocrine system, and other malignancies
  • Severe mental illness
  • Patients deemed unsuitable for inclusion by the investigator

Trial design

15 participants in 2 patient groups

Cohort 1
Description:
Tafa combination therapy group, which could include Tafa combined with lenalidomide, Tafa combined with Lenalidomide plus BTK inhibitors, Tafa combined with Lenalidomide plus chemotherapy (including ADC)
Treatment:
Drug: Tafasitamab Injection
Cohort 2
Description:
Tafa combination therapy group followed by sequential CAR T or transplantation
Treatment:
Drug: Tafasitamab Injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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