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  • NCT06357754

Recruiting

Transgene Assay Testing Service of Tumor Samples From Patients Who Received a Bristol-Myers Squibb Manufactured Gene Modified Cell Therapy and Have a Qualifying Second Primary Malignancy - CA082-085

Oppdatert: 2 juni, 2025   |   ClinicalTrials.gov

Utskriftsvennlig Sammendrag

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  • Kjønn

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    Aldersgruppe

  • 3

    Sted(er)

  • Recruiting

Behandlingsalternativer

Studiearmer
TILDELT INTERVENSJON
Participants treated with idecabtagene vicleucel
Biological: Idecabtagene vicleucel
Participants treated with lisocabtagene maraleucel
Biological: Lisocabtagene maraleucel

Nøkkelkriterier for kvalifikasjon

Inclusion Criteria: - Participant has received a commercially available Bristol-Myers Squibb (BMS) manufactured Gene Modified Cell Therapy (GMCT) and has been diagnosed with a qualifying second primary malignancy or a second primary malignancy which BMS has qualified for testing. - Participant has received a commercially available BMS manufactured GMCT in a clinical trial or other investigational setting (including non-conforming product) for which there is no testing protocol in place for that trial or investigational setting and has been diagnosed with a qualifying second primary malignancy or a second primary malignancy which BMS has qualified for testing. Exclusion Criteria: - Participant is actively participating in a clinical trial where information and sample collection is being conducted under that clinical trial. - Participant has not received a BMS manufactured GMCT or has not been diagnosed with a qualifying second primary malignancy.

Vi anbefaler at du kontakter BMS for å rapportere bivirkninger.
Bivirkninger (uønskede hendelser) og andre rapporterbare hendelser er definert her
For å rapportere bivirkninger (uønskede hendelser) eller reklamere på et legemiddel: Medisinsk informasjon

MLTNO2000046