Non Hodgkin Lymphoma Clinical Trial

Long-term Cognitive, Neuropsychiatric and Functional Outcomes in Adults Who Have Received Chimeric Antigen-Receptor T-Cell (CAR-T) Therapy for Aggressive Lymphoma at Stanford

Summary

This study aims to assess the feasibility of performing neuropsychological testing to measure the cognitive performance of individuals following Axicabtagene ciloleucel CAR-T therapy at Stanford.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

>/= 18 years-old
Treated with Axicabtagene ciloleucel CAR-T therapy at Stanford Or
Treated with standard commercial Axicabtagene ciloleucel CAR-T therapy elsewhere and followed primarily by SHC Blood and Bone Marrow transplant providers
>/= 6 months from the date of CAR-T infusion
Fluent in English
Able to attend and participate in in-person testing (Arm I)
Able to participate in remote video testing with adequate workspace, computer and internet capabilities for a reliable telehealth video connection (Arm II)

Exclusion Criteria:

Concurrent enrollment in a CAR-T therapeutics research study
Unable to be present for the scheduled testing
Unable to participate in testing due to severe cognitive or physical limitation
Actively receiving chemotherapy
Progressive cancer

Study is for people with:

Non Hodgkin Lymphoma

Estimated Enrollment:

20

Study ID:

NCT05416554

Recruitment Status:

Not yet recruiting

Sponsor:

Stanford University

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There is 1 Location for this study

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Stanford Cancer Center
San Francisco California, 94305, United States More Info
Brian J Scott, MD
Contact
[email protected]
[email protected]
Michelle Monje, MD, PhD
Sub-Investigator
Gayle Deutsch, PhD, ABPP
Sub-Investigator
Matthew J Frank, MD, PhD
Sub-Investigator
Sheila Lahijani, MD
Sub-Investigator
Tracy P Murray, MSN, RN, AGACNP-BC
Sub-Investigator

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Estimated Enrollment:

20

Study ID:

NCT05416554

Recruitment Status:

Not yet recruiting

Sponsor:


Stanford University

How clear is this clinincal trial information?

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