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Recruiting

A Study of CC-95251, a Monoclonal Antibody Directed Against SIRPα, in Subjects With Advanced Solid and Hematologic Cancers - CC-95251-ST-001

Actualizada: 16 febrero, 2021   |   ClinicalTrials.gov

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Detalles del estudio

  • Phase 1

    Fase

  • Géneros

  • 18+

    Rango de edad

  • 19

    Ubicación (es)

  • Recruiting

Opciones de tratamiento

Brazos del estudio
INTERVENCIÓN ASIGNADA
Experimental: CC-95251 alone
Drug: CC-95251
Experimental: CC-95251 in combination with cetuximab
Drug: CC-95251 Drug: Cetuximab
Experimental: CC-95251 in combination with rituximab
Drug: CC-95251 Drug: Rituximab

Criterios clave de elegibilidad

Inclusion Criteria: 1. Subject must understand and voluntarily sign an informed consent form (ICF). 2. Subject (male or female) is ≥ 18 years of age at the time of signing the ICF. 3. Subject must have progressed on (or not been able to tolerate due to medical comorbidities or unacceptable toxicity) standard anticancer therapy or for whom no other approved conventional therapy exists and have histological or cytological confirmation of advanced unresectable solid tumors. 4. Subject must have at least one site of measurable disease as determined by RECIST v1.1. NHL subjects must have bi-dimensionally measurable disease on cross sectional imaging by CT or MRI as defined by Lugano/IWG criteria. 5. Subject has an ECOG PS of 0 or 1. 6. Subjects must exhibit acceptable hematopoietic, liver, renal, and coagulation function as assessed by laboratory tests. 7. Subject is willing and able to adhere to the study visit schedule and other protocol requirements. Exclusion Criteria: 1. Subject has received prior investigational therapy directed at CD47 or SIRPα. 2. Subject has cancer with symptomatic central nervous system involvement. 3. Subject is on chronic systemic immunosuppressive therapy or corticosteroids. 4. Subjects with a history of clinically significant cardiac disease within the previous 6 months. 5. Subject had a prior systemic cancer-directed treatments or investigational modalities ≤ 5 half-lives or 4 weeks prior to starting CC-95251, whichever is shorter. 6. Subject had major surgery ≤ 2 weeks prior to starting CC-95251. 7. Subject is a pregnant or lactating female. 8. Subject has known human immunodeficiency virus (HIV) infection. 9. Subject has known chronic, active hepatitis B or C (HBV/HCV) infection. 10. Ongoing treatment with chronic, therapeutic dosing of anti-coagulants. 11. History of autoimmune hemolytic anemia or autoimmune thrombocytopenia. 12. History of concurrent second cancers requiring active, ongoing systemic treatment. 13. For subjects receiving cetuximab, known history of cetuximab intolerance.

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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