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Terminated Phase 1 Interventional Results available

Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of Investigational Treatments in Combination With Standard of Care Immune Checkpoint Inhibitors in Participants With Advanced Melanoma

ClinicalTrials.gov ID: NCT02723006

Public ClinicalTrials.gov record NCT02723006. 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 26, 2026, 6:14 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

An Open-Label, Phase 1b, Multi-Arm Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of Investigational Treatments in Combination With Standard of Care Immune Checkpoint Inhibitors in Patients With Advanced Melanoma

Brief summary

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

The purpose of this study is to determine the initial safety profile and initial antitumor activity of the combination treatments (immune checkpoint inhibitors \[nivolumab, ipilimumab\] with investigational drugs \[TAK-580, TAK-202 (plozalizumab), vedolizumab\]) in the 3 arms when administered to participants with advanced melanoma.

Study identification

NCT ID
NCT02723006
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Enrollment
22 participants

Conditions and interventions

Conditions

Interventions

Drug

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
Jun 22, 2016 (Actual)
Primary completion
May 11, 2018 (Actual)
Completion
May 11, 2018 (Actual)
Last update posted
Mar 5, 2024

2016 – 2018

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
University of Arizona Cancer Center Tucson Arizona — —
University of California Los Angeles - Jonsson Comprehensive Cancer Center Los Angeles California — —
University of California San Francisco Medical Center San Francisco California — —
University of Colorado Cancer Center Aurora Colorado — —
Emory University Hospital Atlanta Georgia — —
Dana-Farber Cancer Institute Boston Massachusetts — —
Massachusetts General Hospital Cancer Center Boston Massachusetts — —
Virginia Piper Cancer Institute Minneapolis Minnesota — —
Washington University School of Medicine St Louis Missouri — —
New York University Langone Medical Center New York New York — —
Saint Luke's Cancer Center - Bethlehem Easton Pennsylvania — —
Fox Chase Cancer Center Philadelphia Pennsylvania — —
Texas Oncology-Baylor Charles A. Sammons Cancer Center Dallas Texas — —
Inova Fairfax Hospital Fairfax Virginia — —

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 NCT02723006, 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 Mar 5, 2024 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02723006 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →