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The CAROLYN Trial: Lisocabtagene Maraleucel as First-Line Therapy for Primary Central Nervous System Lymphoma (PCNSL) in Transplant-Ineligible Patients

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521144-38-00
Acronym
CA082-1215
Enrollment
31
Registered
2025-10-29
Start date
2025-12-23
Completion date
Unknown
Last updated
2025-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Central Nervous System Lymphoma

Brief summary

The proportion of participants in whom the cancer gets worse, or who passed away, within 12 months after getting liso-cel.

Detailed description

The time it takes for the cancer to worsen, The time it takes for the participant to start a new cancer treatment, The time it takes for the participants to pass away, after they enroll into the study;, The proportion of participants with no detectable signs of cancer, The proportion of participants with improvement in signs (complete and partial responses), at any time after getting the liso-cel treatment and before the cancer gets worse, they start a new cancer treatment, or the study ends, How long the responses last, How the treatment affects the participants' quality of life, What kinds of health problems participants experience during the study, how severe they are, and how often they happen

Interventions

DRUGTEMOZOLOMIDE
DRUGMETHOTREXATE
DRUGPROCARBAZINE
DRUGCALCIUM FOLINATE
DRUGRITUXIMAB
DRUGFLUDARABINE
DRUGCYCLOPHOSPHAMIDE
DRUGTOCILIZUMAB

Sponsors

Bristol-Myers Squibb Services Unlimited Company
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The proportion of participants in whom the cancer gets worse, or who passed away, within 12 months after getting liso-cel.

Secondary

MeasureTime frame
The time it takes for the cancer to worsen, The time it takes for the participant to start a new cancer treatment, The time it takes for the participants to pass away, after they enroll into the study;, The proportion of participants with no detectable signs of cancer, The proportion of participants with improvement in signs (complete and partial responses), at any time after getting the liso-cel treatment and before the cancer gets worse, they start a new cancer treatment, or the study ends, How long the responses last, How the treatment affects the participants' quality of life, What kinds of health problems participants experience during the study, how severe they are, and how often they happen

Countries

France, Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026