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Recruiting

Prospective Research Assessment in Multiple Myeloma: An Observational Evaluation (PREAMBLE) - CA204-008

Actualizada: 5 mayo, 2022   |   ClinicalTrials.gov

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Detalles del estudio

  • Géneros

  • 18+

    Rango de edad

  • 24

    Ubicación (es)

  • Recruiting

Opciones de tratamiento

Brazos del estudio
INTERVENCIÓN ASIGNADA
Cohort 1
Cohort 1
Cohort 2
Combination novel therapies
New Agents

Criterios clave de elegibilidad

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: For RRMM participants who have received at least one prior line of therapy (LoT) for MM: - Have documented progression from a prior LoT - Participants who have initiated treatment with one of the following therapies within 90 days before consent for this study OR in the case where treatment has not yet been initiated, documentation that the treatment strategy was determined before consent for this study must be provided, and treatment must be initiated within 30 days after consent: - IMiDs - PIs - Combination of IMiD + PI - Newer agents with novel MOAs alone or in combination (eg, mAbs, HDACIs, Akt inhibitors, SINE, or CAR T-cell therapies) For NDMM participants receiving frontline therapy: - Eligible to receive frontline therapy for MM (no prior MM treatment) - Participants who have initiated treatment for MM with one of the following therapies within 90 days before consent for this study OR in the case where treatment has not yet been initiated, documentation that the treatment strategy was determined before consent for this study must be provided, and treatment must be initiated within 30 days after consent: - IMiDs - PIs - Combination of IMiD + PI - Newer agents with novel MOAs alone or in combination (eg, mAbs, HDACIs, Akt inhibitors, SINE, or CAR T-cell therapies) Exclusion Criteria: - Participants who are currently participating in a clinical trial for MM - Participants who are currently receiving treatment for primary cancer other than MM - Participants who are not willing or able to provide informed consent - Participants who are incarcerated - Participants under compulsory detention for treatment of a physical (eg, infectious) or psychiatric illness Other protocol-defined inclusion/exclusion criteria apply

Recomendamos encarecidamente que se comunique con BMS para informar los efectos secundarios (eventos adversos)
Los efectos secundarios (eventos adversos) y otros eventos reportables se definen aquí
Informe de efectos secundarios (eventos adversos) o quejas sobre la calidad del producto: información médica

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