drugset / Trial / NCT02960854

A Study of Nivolumab Safety and Pharmacokinetics in Patients With Severe Sepsis or Septic Shock.

NCT02960854 ↗

Phase 1 Completed 38 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindOther

Summary

A study to evaluate the safety, tolerability and pharmacokinetics of Nivolumab in participants with severe sepsis or septic shock.

Timeline

Start
2016-12-07
Primary completion
2018-01-05
Completion
2018-01-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 480 mg —
Subject Nivolumab Monoclonal antibody 960 mg —