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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 May 11, 2026, 2:32 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

Study identification

NCT ID
NCT02723006
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Millennium Pharmaceuticals, Inc.
Industry
Enrollment
22 participants

Conditions and interventions

Conditions

Interventions

  • TAK-202 Drug
  • TAK-580 Drug
  • ipilimumab Drug
  • nivolumab Drug
  • vedolizumab Drug

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 21, 2016
Primary completion
May 10, 2018
Completion
May 10, 2018
Last update posted
Mar 4, 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 4, 2024 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02723006 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →