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Completed Phase 1 Interventional Results available

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

ClinicalTrials.gov ID: NCT02960854

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT02960854. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 13, 2026, 2:55 PM EST

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Official title

Randomized, Double-Blind, Parallel Group Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BMS-936558 (Nivolumab) in Participants With Severe Sepsis or Septic Shock.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT02960854
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
38 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 7, 2016 (Actual)
Primary completion
Jan 5, 2018 (Actual)
Completion
Jan 5, 2018 (Actual)
Last update posted
Apr 23, 2019

2016 – 2018

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Uc Davis Medical Center Sacramento California 95817 —
Univ. Of Colorado Health Colorado Springs Colorado 80909 —
Denver Health Medical Center Denver Colorado 80204 —
University Of Florida Gainesville Florida 32610 —
Pulmonary And Critical Care Of Atlanta Atlanta Georgia 30303 —
Osf Saint Francis Medical Center Peoria Illinois 61637 —
University Of Kentucky Lexington Kentucky 40536 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Beth Israel Deaconess Medical Center (BIDMC) Boston Massachusetts 02215 —
Baystate Medical Center Springfield Massachusetts 01199 —
University of Michigan, Division of Acute Care Surgery Ann Arbor Michigan 48109-5008 —
Washington University School Of Medicine St Louis Missouri 63110 —
Duke University Medical Center Durham North Carolina 27710 —
The Ohio State University Columbus Ohio 43210 —
UPMC Pittsburgh Pennsylvania 15261-2500 —
Harborview Medical Center Seattle Washington 98104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02960854, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 23, 2019 · Synced Nov 13, 2026

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