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Hledat Study Connect

Active, Not Recruiting

An Investigational Immuno-Therapy Study to Determine the Safety and Effectiveness of Nivolumab and Daratumumab in Patients With Multiple Myeloma - CA209-039

Aktualizováno: 11 září, 2023   |   ClinicalTrials.gov

Kontaktujte nás, potřebujete-li pomoc
clinical.trials@bms.com

Tisk přehledného shrnutí

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Podrobnosti o hodnocení

  • Phase 1/Phase 2

    Fáze

  • Pohlaví

  • 18+

    Věková skupina

  • Active, Not Recruiting

Možnosti léčby

Ramena studie
Přiřazená léčba
Experimental: Daratumumab vs. Nivolumab + Daratumumab
Biological: Nivolumab, Daratumumab
Experimental: Nivo + Dara + Pom + Dexa vs. Nivo + Dara
Biological: Nivolumab, Daratumumab Drug: Pomalidomide, Dexamethasone
Experimental: Nivolumab + Ipilimumab
Biological: Ipilimumab, Nivolumab
Experimental: Nivolumab + Lirilumab
Biological: Nivolumab, Lirilumab
Experimental: Nivolumab monotherapy (Dose Escalation)
Biological: Nivolumab

Klíčová kritéria způsobilosti

For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Have received at least 3 prior lines of therapy, including a proteasome inhibitor [PI] and an immunomodulatory agent [IMiD] OR have disease that is double refractory to a PI and IMiD - More than 12 weeks post-transplant of your own blood forming stem cells (autologous transplant) - Have detectable disease measured by a specific protein in your blood and/or urine - Must consent to bone marrow aspirate or biopsy. Exclusion Criteria: - Solitary bone or extramedullary plasmacytoma as the only evidence of plasma cell dyscrasia, or monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), primary amyloidosis, Waldenstrom's macroglobulinemia, POEMS syndrome or active plasma cell leukemia - Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, anti CTLA 4, or anti-CD38 antibody, or allogeneic stem cell transplantation - Seropositive for human immunodeficiency virus (HIV), Hepatitis B surface antigen or Hepatitis C antibody positive (except if HCV-RNA negative), or history of active chronic hepatitis B or C - History of central nervous system involvement or symptoms suggestive of central nervous system involvement by multiple myeloma Other protocol defined inclusion/exclusion criteria could apply

Důrazně doporučujeme kontaktovat BMS a oznámit vedlejší účinky / nežádoucí příhody
Zde jsou definovány vedlejší účinky / nežádoucí příhody a další příhody, které by měly být hlášeny
Nahlásit vedlejší účinky / nežádoucí příhody nebo stížnosti na kvalitu produktu: lékařské informace

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