Share Icon Health Study Area: Cardiovascular Disease Chevron Icon Health Study Area: Genitourinary For Patients Health Study Area: Lung Cancer Page Icon Phone Icon For Caregivers Health Study Area: AutoImmune Disease Health Study Area: Melanoma Location Icon Print YouTube Icon For Parents Health Study Area: Lung Cancer Print Created with Sketch. Help Icon Green Check Icon Search Icon Instagram Created with sketchtool. Direction Arrow Icon Error Icon For Parents Health Study Area: Blood Cancer Help Icon Health Study Area: NASH Gender Both Bookmark Icon Health Study Area: Melanoma Created with Sketch. Glossary Print Health Study Area: Blood Cancer Health Study Area: Genitourinary Health Study Area: Gastrointestinal Cancer Mobile Menu Icon Created with Sketch. Health Study Area: Cardiovascular Disease Health Study Area: Women's Cancer Communities Map Icon Created with Sketch. For Caregivers Health Study Area: Fibrosis Health Study Area: AutoImmune Disease FAQs Health Study Area: Head and Neck Cancer Created with Sketch. For Clinicians Chevron Right Icon Gender Female Health Study Area: Breast Cancer Direction Arrow Icon Gender Both Right Arrow Icon LinkedIn Icon Green Check Icon Gender Male Health Study Area: Fibrosis For Patients Twitter Icon Email Icon Facebook Icon Health Study Area: Gastrointestinal Cancer Health Study Area: Head and Neck Cancer For Clinicians External Link Icon

Menü

Klinische Studien von BMS suchen
BMS-Symbol für "Aktive Studie, für die noch nicht rekrutiert wird"

Active, Not Recruiting

Studien-Nr. CC-95251-ST-001  |   NCT03783403

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

Celgene ist eine reine Tochtergesellschaft von Bristol-Myers Squibb

Warnsymbol
In diese Studie werden leider keine neuen Patient:innen aufgenommen, sie ist aber weiterhin aktiv.
Sie können auf die Schaltfläche "Prüfen Sie, ob eine Studie für Sie infrage kommt“ und einige Fragen zu Ihrer Gesundheit beantworten, um herauszufinden, ob eine andere Studie für Sie infrage kommt.

Zusammenfassung

  • Phase 1
  • Symbol für männliches und weibliches Geschlecht
  • 18+
    Altersgruppe
  • BMS-Symbol für "Aktive Studie, für die noch nicht rekrutiert wird"
    Active, Not Recruiting

Überblick

Study CC-95251-ST-001 is an open-label, Phase 1, dose escalation (Part A) and expansion (Parts B and C), first-in-human clinical study of CC-95251 in subjects with advanced cancers.

Wichtigste Einschlusskriterien

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.

Behandlungsmöglichkeiten

Studienarme

ZUGEWIESENE BEHANDLUNG

Studienarme

Experimental: CC-95251 alone

ZUGEWIESENE BEHANDLUNG
  • Drug: CC-95251

Studienarme

Experimental: CC-95251 in combination with cetuximab

ZUGEWIESENE BEHANDLUNG
  • Drug: CC-95251, Cetuximab

Studienarme

Experimental: CC-95251 in combination with rituximab

ZUGEWIESENE BEHANDLUNG
  • Drug: CC-95251, Rituximab

Unterstützen Sie uns dabei, Ihre Nutzung der Website zu optimieren! Teilen Sie Ihr Feedback mit unserem Team bei BMS Clinical Trials, um die Nutzung der Webseite, Ihre Erfahrungen und die anderer zu verbessern. Vielen Dank!