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Study details
Enrolling now

A Study of Lisocabtagene Maraleucel (Liso-cel) for Transplant-Ineligible PCNSL

Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
NCT IDNCT07015242ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

65

Study length

about 3.1 years

Ages

18+

Locations

30 sites in CA, CO, FL +10

Why this study is shown

Actively enrollingPHASE2

What this study is about

Researchers are testing the safety and effectiveness of a treatment called lisocabtagene maraleucel (liso-cel) in adults with transplant-ineligible Primary Central Nervous System Lymphoma (PCNSL). The trial will last about 1130 days.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive Liso-cel
  • 2.Take Calcium folinate
  • 3.Take Cyclophosphamide
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVOral

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

calcium folinate, cyclophosphamide (Alkylating chemotherapy; crosslinks DNA strands), fludarabine, methotrexate, procarbazine, rituximab (Monoclonal antibody; targets CD20 on B-cells to destroy them), temozolomide

Drug routes

infusion, oral (Oral Tablet), oral (Oral Capsule), injection, intravenous

Endpoints

Primary: Progression-free Survival (PFS)

Secondary: Complete Response Rate (CRR), Duration of Response (DoR), Event-free Survival (EFS), Health-related quality of life (HRQoL), Modified Progression-free Survival (mPFS), Overall Response Rate (ORR), Overall Survival (OS), PFS

Body systems

Oncology