drugset / Trial / NCT01375842

A Study of Atezolizumab (an Engineered Anti-Programmed Death-Ligand 1 [PDL1] Antibody) to Evaluate Safety, Tolerability and Pharmacokinetics in Participants With Locally Advanced or Metastatic Solid Tumors

NCT01375842 ↗

Phase 1 Completed 661 enrolled Genentech, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This Phase I, multicenter, first-in-human, open-label, dose-escalation study will evaluate the safety, tolerability, and pharmacokinetics of atezolizumab (MPDL3280A) administered as single agent to participants with locally advanced or metastatic solid malignancies or hematologic malignancies. The study will be conducted in two cohorts: Dose-escalation cohort and Expansion cohort.

Timeline

Start
2011-06-21
Primary completion
2018-09-30
Completion
2018-09-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Atezolizumab Monoclonal antibody 0.01 mg/kg Intravenous
Subject Atezolizumab Monoclonal antibody 0.03 mg/kg Intravenous
Subject Atezolizumab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Atezolizumab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Atezolizumab Monoclonal antibody 1 mg/kg Intravenous
Subject Atezolizumab Monoclonal antibody 3 mg/kg Intravenous
Subject Atezolizumab Monoclonal antibody 10 mg/kg Intravenous
Subject Atezolizumab Monoclonal antibody 20 mg/kg Intravenous