A Study to Evaluate Zanubrutinib and Tislelizumab in Progressive Lymphoma Post CAR-T

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Health Network, Toronto

About this trial

This is a phase ll study of participants with large B Cell lymphoma previously treated with anti-CD19 Chimeric antigen receptor (CAR-T) therapy. The purpose of the study is to to evaluate the efficacy of zanubrutinib and tislelizumab in patients with progressive lymphoma post anti-CD 19 CAR-T failure.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Able and willing to provide written informed consent and to comply with the study protocol

Radiologically measurable disease (≥ 1 nodal lesion > 2.0 cm in the longest diameter, and/or extranodal lesion > 1.0cm in the longest diameter)

Intervention arm: Radiological measurable disease per inclusion criterion #3 with more than one site of disease.

Disqualifiers

Life expectancy < 30 days at the time of enrollment

Prior exposure to BTK or PD-1 inhibitor at any time prior to enrollment

Prior anaphylactic reaction to monoclonal antibody therapy at any time prior to enrollment

Intervention arm: On higher than physiologic doses (10mg daily) of prednisone daily at least 7 days prior to initiation of trial treatment. SOC arm: On prednisone for symptom management only.

Trial design

Treatments tested in this trial

  • Tislelizumab
  • Zanubrutinib
  • Tislelizumab + Zanubrutinib

Treatment groups

76 Participants
are divided into 4 treatment groups