Zanubrutinib in Combination With Pola-R-CHP and High-dose Methotrexate in Patients With Secondary CNS Lymphoma

PHASE1RecruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

April 17, 2025

Primary Completion Date

April 30, 2030

Study Completion Date

April 30, 2030

Conditions
CNS Lymphoma
Interventions
DRUG

Zanubrutinib

Zanubrutinib capsules will be self-administered orally by participants at a starting dose of 160 mg twice a day (BID) or 320 mg once a day (QD)\* at the beginning of Cycle 2 of Pola-R-CHP therapy.

DRUG

Methotrexate

Participants will receive Methotrexate as per standard of care (SOC).

DRUG

Polatuzumab Vedotin

Participants will receive Polatuzumab Vedotin as per standard of care (SOC).

DRUG

Rituximab

Participants will receive Rituximab as per standard of care (SOC), as part of combination standard of care Pola-R-CHP therapy.

DRUG

Cyclophosphamide

Participants will receive Cyclophosphamide as per standard of care (SOC), as part of combination standard of care Pola-R-CHP therapy.

DRUG

Doxorubicin

Participants will receive Doxorubicin as per standard of care (SOC), as part of combination standard of care Pola-R-CHP therapy.

DRUG

Prednisone

Participants will receive Prednisone as per standard of care (SOC), as part of combination standard of care Pola-R-CHP therapy.

Trial Locations (1)

33136

RECRUITING

University of Miami, Miami

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

BeiGene

INDUSTRY

lead

Juan P. Alderuccio, MD

OTHER

NCT06730542 - Zanubrutinib in Combination With Pola-R-CHP and High-dose Methotrexate in Patients With Secondary CNS Lymphoma | Biotech Hunter | Biotech Hunter