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NCT07015242 · ClinicalTrials.gov registry record · Phase 2

A Study of the Efficacy and Safety of Lisocabtagene Maraleucel (Liso-cel) as First-Line Therapy in Adults With Transplant-Ineligible Primary Central Nervous System Lymphoma

A Phase 2 study of Lymphoma, sponsored by Juno Therapeutics, Inc., a Bristol-Myers Squibb Company.

Recruiting
Registry status
Phase 2
Development phase
65
Enrollment target
20
Study locations

NCT07015242: Recruiting Phase 2 study of Lymphoma, sponsored by Juno Therapeutics, Inc., a Bristol-Myers Squibb Company.

NCT07015242 is a Phase 2 study of Lymphoma that is actively recruiting participants, run by Juno Therapeutics, Inc., a Bristol-Myers Squibb Company. The registered enrollment target is 65 participants, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (87% lower). The trial reports 20 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07015242, a Phase 2 study of Lymphoma, is actively recruiting participants, sponsored by Juno Therapeutics, Inc., a Bristol-Myers Squibb Company.

RECRUITING
Registry status
Phase 2
Development phase
65 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this study is to evaluate the safety and efficacy of lisocabtagene maraleucel (Breyanzi/liso-cel/BMS-986387) in adults as first-line treatment in transplant-ineligible Primary Central Nervous System Lymphoma (PCNSL).

Primary Outcome

Defined as the time from the date of liso-cel infusion to the date of first documented disease relapse or progression as assessed by the investigator, or death from any cause, whichever occurs first

Conditions Studied

Interventions

  • DRUG Rituximab
  • DRUG Temozolomide
  • DRUG Methotrexate
  • DRUG Procarbazine
  • BIOLOGICAL Liso-cel

Study Locations (20)

New York

  • Local Institution - 310 - Buffalo
  • Roswell Park Comprehensive Cancer Center - Buffalo
  • Local Institution - 301 - New York
  • Memorial Sloan Kettering Cancer Center - New York

Massachusetts

  • Local Institution - 314 - Boston
  • Dana-Farber Cancer Institute - Boston
  • Local Institution - 313 - Boston

Colorado

  • Local Institution - 0305 - Aurora
  • Local Institution - 305 - Aurora

Florida

  • Local Institution - 308 - Tampa
  • Moffitt Cancer Center - Tampa

Illinois

  • Local Institution - 0311 - Chicago
  • Local Institution - 311 - Chicago

Missouri

  • Local Institution - 316 - St Louis
  • Washington University School of Medicine in St. Louis - St Louis

New Jersey

  • Local Institution - 0315 - New Brunswick
  • Local Institution - 315 - New Brunswick

Ohio

  • Cleveland Clinic - Cleveland
  • Local Institution - 302 - Cleveland

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2025-11-06
Est. Completion 2028-12-10
Phase Phase 2

What NCT07015242 shows while recruiting

NCT07015242 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 484-participant average among 299 other Lymphoma trials with a reported enrollment target (87% lower).

The record links to 1 condition, with Lymphoma appearing as the primary indexed condition, and to 5 interventions - of which Rituximab is the first listed.

NCT07015242 names 20 study sites across 9 states, led by New York, Massachusetts, Colorado.

Frequently Asked Questions

What is clinical trial NCT07015242 about?

NCT07015242 is a clinical study titled "A Study of the Efficacy and Safety of Lisocabtagene Maraleucel (Liso-cel) as First-Line Therapy in Adults With Transplant-Ineligible Primary Central Nervous System Lymphoma". The purpose of this study is to evaluate the safety and efficacy of lisocabtagene maraleucel (Breyanzi/liso-cel/BMS-986387) in adults as first-line treatment in transplant-ineligible Primary Central Nervous System Lymphoma (PCNSL).

What is the current status of trial NCT07015242?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 65 participants. The study started on 2025-11-06. Estimated completion is 2028-12-10.

What conditions does trial NCT07015242 study?

This clinical trial studies the following conditions: Lymphoma.

What interventions are being tested in trial NCT07015242?

The interventions under investigation include: Rituximab (DRUG), Temozolomide (DRUG), Methotrexate (DRUG), Procarbazine (DRUG), Liso-cel (BIOLOGICAL).

Who is sponsoring clinical trial NCT07015242?

This trial is sponsored by Juno Therapeutics, Inc., a Bristol-Myers Squibb Company, which has 14 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07015242 being conducted?

This trial has 20 study locations across California, Colorado, Florida, Illinois, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lymphoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07015242's enrollment target sits among peer trials

65 122nd of 299 higher than 177 of 299 other Lymphoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Lymphoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT07015242, the US trial registry maintained by the National Library of Medicine. NCT07015242 (small enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.