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Voice as a Digital Biomarker of Neurotoxicity in CAR T-Cell Therapy

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The purpose of this study is to collect voice recordings and nervous system (neurologic) assessments from people with non-Hodgkin lymphoma (NHL) or multiple myeloma (MM) who are receiving standard treatment with CAR T-cell therapy. Researchers will study whether these voice recordings and assessments are a practical (feasible) way to monitor for immune effector cell-associated neurotoxicity syndrome (ICANS). Feasibility will be measured by tracking how many participants join the study and complete the assessments.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Documentation of Disease

• o Patients must have pathologically confirmed Diagnosed with non-Hodgkin lymphoma or multiple myeloma.

• Definition of treatment and ability

‣ Scheduled to receive an FDA-approved CAR-T product: Axi-cel, Liso-cel, Tisa-cel, Ide-cel, Cilta-cel, or Brexu-cel.

⁃ Ability to comply with twice daily voice recordings or daily neurologic assessments, as determined by the investigator.

• Age ≥ 18

• ECOG Performance Status of ≤ 2

• Required

‣ Perform twice daily voice recordings using a smartphone.

⁃ Undergo daily neurologic assessments (e.g., ICE score, tremor evaluation).

⁃ Smartphone ownership.

⁃ Sufficient English proficiency to complete structured voice tasks in the study application.

• Comorbid Conditions

‣ No pre-existing neurological conditions that significantly impair speech, including but not limited to severe dysarthria, expressive aphasia, or neurodegenerative disorders.

⁃ No history of significant speech or voice disorders, including laryngeal paralysis, severe dysphonia, or recent vocal cord surgery or radiation to the area.

⁃ No pathology affecting the vocal cords that could interfere with voice analysis, such as vocal cord paralysis, chronic laryngitis, vocal cord nodules, polyps, granulomas, or malignancies.

⁃ No severe hearing impairment that would interfere with voice assessments

• Language o Proficiency in spoken English is required, without the need for native-level fluency. This ensures participants can accurately perform structured voice tasks, as the application and underlying acoustic models are currently validated only in English, despite the limitation in generalizability. Participants with language barriers that prevent reliabletask completion or data interpretation will be excluded.

Locations
United States
New Jersey
Memorial Sloan Kettering at Basking Ridge (Consent Only)
RECRUITING
Basking Ridge
Memorial Sloan Kettering Monmouth (Consent only)
RECRUITING
Middletown
Memorial Sloan Kettering Bergen (Consent Only)
RECRUITING
Montvale
New York
Memorial Sloan Kettering Suffolk-Commack (Consent Only)
RECRUITING
Commack
Memorial Sloan Kettering Westchester (Consent only)
RECRUITING
Harrison
Memorial Sloan Kettering Cancer Center (All Protocol Activites)
RECRUITING
New York
Weill Cornell Medical Center (Data Analysis Only)
NOT_YET_RECRUITING
New York
Memorial Sloan Kettering Nassau (Consent Only)
RECRUITING
Rockville Centre
Contact Information
Primary
Roni Shouval, MD, PhD
shouvalr@mskcc.org
646-888-3483
Backup
Mohammad Alhomoud, MD
alhomom@mskcc.org
646-608-4375
Time Frame
Start Date: 2026-04-17
Estimated Completion Date: 2027-12
Participants
Target number of participants: 20
Treatments
Participants diagnosed with non-Hodgkin lymphoma or multiple myeloma
Participants must have pathologically confirmed Diagnosed with non-Hodgkin lymphoma or multiple myeloma.
Sponsors
Leads: Memorial Sloan Kettering Cancer Center

This content was sourced from clinicaltrials.gov