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Clear Cell Renal Cell CarcinomaCancerKidney and urinaryBiologicalPhase 1

What this study is

The purpose of this study is to assess the safety and tolerability of XmAb®819 administered intravenous (IV) or subcutaneous (SC) in subjects with relapsed or refractory clear cell renal cell carcinoma and to identify the minimum safe and biologically active dose and the recommended dose (RD).

What's being tested

  • XmAb819

    Intervention · BIOLOGICAL

    Monoclonal Bispecific Antibody

Study details

Official title
A Phase 1 Multiple Dose Study to Evaluate the Safety and Tolerability of XmAb819 in Subjects With Relapsed or Refractory Clear Cell Renal Cell Carcinoma
Sponsor
Xencor, Inc.
Conditions
Clear Cell Renal Cell Carcinoma
Enrolling
307 people
Starts
2022-06-13
Est. completion
2028-12
Design
Open-label, sequential groups, Phase 1
Record
View on ClinicalTrials.gov ↗