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Suspended Phase 1Phase 2 Interventional

A Study to Evaluate Lucitanib in Combination With Nivolumab in Patients With a Solid Tumor

ClinicalTrials.gov ID: NCT04042116

Public ClinicalTrials.gov record NCT04042116. 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 Oct 28, 2026, 3:30 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

LIO-1: A Phase 1b/2, Open-Label Study to Evaluate the Safety and Efficacy of Lucitanib in Combination With Nivolumab in Patients With An Advanced, Metastatic Solid Tumor

Brief summary

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

This is an open-label, Phase 1b/2 study to determine the recommended dose of lucitanib in combination with nivolumab in patients with an advanced solid tumor (Phase 1b); followed by evaluation of the safety and efficacy of lucitanib and nivolumab in patients with an advanced gynecological solid tumor (Phase 2) and evaluate the effects of dosing under fasting or fed state (Food Effect)

Study identification

NCT ID
NCT04042116
Recruitment status
Suspended
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Clovis Oncology, Inc.
Industry
Enrollment
227 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
Jul 29, 2019 (Actual)
Primary completion
Jul 2023 (Estimated)
Completion
Jan 2024 (Estimated)
Last update posted
Dec 20, 2022

2019 – 2024

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
UCLA Jonsson Comprehensive Cancer Center Los Angeles California 90095 —
UC San Diego Moores Cancer Center San Diego California 92093 —
Anschutz Cancer Pavilion Aurora Colorado 80045 —
Florida Cancer Specialists Sarasota Florida 34232 —
Massachusetts General Hospital Boston Massachusetts 02114 —
NYU Langone Laura and Isaac Perlmutter Cancer Center New York New York 10016 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Duke University School of Medicine Durham North Carolina 27710 —
Ohio State University Wexner Medical Center Columbus Ohio 43210 —
Stephenson Cancer Center Oklahoma City Oklahoma 73104 —
Magee-Womens Hospital of UPMC Pittsburgh Pennsylvania 15213 —
Tennessee Oncology Nashville Tennessee 37203 —
Swedish Cancer Institute Seattle Washington 98107 —

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 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04042116, 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 Dec 20, 2022 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04042116 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →