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Terminated Phase 1Phase 2 Interventional Results available

A Study of Rovalpituzumab Tesirine Administered in Combination With Nivolumab and With or Without Ipilimumab for Adults With Extensive-Stage Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT03026166

Public ClinicalTrials.gov record NCT03026166. 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 24, 2026, 8:14 PM 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 1/2 Study on the Safety of Rovalpituzumab Tesirine Administered in Combination With Nivolumab or Nivolumab and Ipilimumab for Adults With Extensive-Stage Small Cell Lung Cancer

Brief summary

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

The purpose of this study is to assess the safety and efficacy of rovalpituzumab tesirine administered in combination with nivolumab or nivolumab and ipilimumab in participants with extensive-stage small cell lung cancer (SCLC).

Study identification

NCT ID
NCT03026166
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
42 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
Mar 29, 2017
Primary completion
Jul 2, 2019
Completion
Jul 2, 2019
Last update posted
Jul 16, 2020

2017 – 2019

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
14
Facility City State ZIP Site status
Ucsd /Id# 161030 La Jolla California 92093 —
Florida Hospital /ID# 161017 Orlando Florida 32803 —
University Cancer & Blood Cent /ID# 161028 Athens Georgia 30607 —
University of Chicago /ID# 161006 Chicago Illinois 60637-1443 —
The University of Kansas Clini /ID# 162915 Fairway Kansas 66205 —
Washington University-School of Medicine /ID# 161011 St Louis Missouri 63110 —
Rutgers Cancer Institute of NJ /ID# 161032 New Brunswick New Jersey 08903 —
Memorial Sloan Kettering Cancer Center /ID# 161010 New York New York 10065-6007 —
Duke University Medical Center /ID# 161009 Durham North Carolina 27710-3000 —
Oregon Health and Science University /ID# 161029 Portland Oregon 97239 —
Medical University of South Carolina /ID# 161007 Charleston South Carolina 29425 —
Tennessee Oncology, PLLC /ID# 161012 Nashville Tennessee 37203 —
Vanderbilt University Med Ctr /ID# 162916 Nashville Tennessee 37232-6307 —
Virginia Cancer Institute /ID# 161025 Richmond Virginia 23230 —
University of Wisconsin Clinic /ID# 161013 Madison Wisconsin 53705 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03026166, 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 Jul 16, 2020 · Synced Sep 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03026166 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →