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Completed Phase 1 Interventional

Safety Study of Nivolumab With Nab-Paclitaxel Plus or Minus Gemcitabine in Pancreatic Cancer, Nab-Paclitaxel / Carboplatin in Stage IIIB/IV Non-Small Cell Lung Cancer or Nab-Paclitaxel in Recurrent Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT02309177

Public ClinicalTrials.gov record NCT02309177. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 26, 2026, 4:16 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1, Open-label, Multicenter, Safety Study of Nivolumab (Bms-936558) in Combination With Nab-pacitaxel Plus or Minus Gemcitabine in Pancreatic Cancer, Nab-paclitaxel/Carboplatin in Stage Iiib/iv Non-small Cell Lung Cancer or Nab-paclitaxel in Metastastic Breast Cancer

Brief summary

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

The purpose of this study is to assess safety of nab-paclitaxel based chemotherapy regimens administered prior to and/or in combination with nivolumab in Pancreatic Cancer, Non Small Cell Lung Cancer (NSCLC) and Metastatic Breast Cancer (mBC).

Study identification

NCT ID
NCT02309177
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Celgene
Industry
Enrollment
114 participants

Conditions and interventions

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
Jan 11, 2015
Primary completion
Sep 11, 2018
Completion
Sep 11, 2018
Last update posted
May 30, 2019

2015 – 2018

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
UC Davis Cancer Center Sacramento California 95817 —
University of California Los Angeles Santa Monica California 90404 —
Yale Cancer Center New Haven Connecticut 06510 —
H. Lee Moffitt Cancer Center and Research Institute University of South Florida Tampa Florida 33612 —
Northwestern University-NMDTI Chicago Illinois 60611 —
Dana-Farber / Harvard Cancer Institute Boston Massachusetts 02114 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
John Theurer Cancer Center at Hackensack University Medical Center Hackensack New Jersey 07601 —
Regional Care Cancer Centers NJ Morristown New Jersey 79062 —
Levine Cancer Institute Charlotte North Carolina 28204 —
Oncology Hematology Care, Inc. Cincinnati Ohio 45242 —
Ohio State Medical Center Columbus Ohio 43210 —
University of Pennslyvania Philadelphia Pennsylvania 19104 —
Seattle Cancer Center Alliance Seattle Washington 98109 —
Medical College of Wisconsin Milwaukee Wisconsin 53226 —

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 NCT02309177, 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 May 30, 2019 · Synced Sep 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02309177 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →