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  • Outcomes of Low-Risk Endometrial Cancer with Isolated Tumor Cells in the Sentinel Lymph Nodes: a Prospective, Multicenter, Cohort Study

    PRIMARY OBJECTIVE: I. Evaluate whether patients with low-risk endometrial cancer and isolated tumor cells (ITC) will have worse recurrence-free survival (RFS) than a historical cohort of similar patients with negative nodes. OUTLINE: This is an observational study. Patients undergo tissue sample collection and have their medical records reviewed on study.

    Phase

    N/A

    Span

    256 weeks

    Sponsor

    Mayo Clinic

    Kefar Sava

    Recruiting

  • Mirvetuximab Soravtansine With Bevacizumab Versus Bevacizumab as Maintenance in Platinum-sensitive Ovarian, Fallopian Tube, or Peritoneal Cancer

    Mirvetuximab Soravtansine (MIRV) is an investigational antibody drug conjugate designed to selectively kill cancer cells. The antibody (protein) part of MIRV targets tumors by delivering a cell-killing drug to the tumor cells carrying a tumor-associated protein called folate receptor alpha (FRα). It is being developed as maintenance therapy for the treatment of subjects with recurrent platinum-sensitive, highgrade epithelial ovarian, primary peritoneal, or fallopian tube cancers with high folate receptor-alpha expression. Patients must have confirmation of FRα positivity by the Ventana FOLR1 Assay.

    Phase

    3

    Span

    331 weeks

    Sponsor

    AbbVie

    Kefar Sava

    Recruiting

  • Disitamab Vedotin With Pembrolizumab vs Chemotherapy in Previously Untreated Urothelial Cancer Expressing HER2

    Phase

    3

    Span

    293 weeks

    Sponsor

    Seagen, a wholly owned subsidiary of Pfizer

    Kefar Sava

    Recruiting

  • Observational Evaluation of Atopic Dermatitis in Pediatric Patients

    The study duration is 120 months.

    Phase

    N/A

    Span

    871 weeks

    Sponsor

    Sanofi

    Kefar Sava

    Recruiting

  • Treatment of Type 1 Diabetes With Anti-OX40L Bispecific With Anti-TNF Activity In a Single Nanobody® Molecule

    The total study duration will be up to 83 weeks including Screening and Safety follow-up period.

    Phase

    2

    Span

    185 weeks

    Sponsor

    Sanofi

    Kefar Sava

    Recruiting

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