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Terminated Phase 1Phase 2 Interventional

A Study of Varlilumab (Anti-CD27) and Ipilimumab and CDX-1401 in Patients With Unresectable Stage III or IV Melanoma

ClinicalTrials.gov ID: NCT02413827

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT02413827. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 15, 2026, 3:42 AM EST

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Official title

A Phase 1 Safety Pilot/Phase II, Open-label Study of Varlilumab (CDX-1127) in Combination With Ipilimumab and CDX-1401 in Patients With Unresectable Stage III or Stage IV Melanoma

Brief summary

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

This is a study to determine the clinical benefit (how well the drug works), safety and tolerability of combining a) varlilumab and ipilimumab and b) varlilumab, ipilimumab, CDX-1401 and poly-ICLC. The study will enroll patients with unresectable Stage III or Stage IV melanoma.

Study identification

NCT ID
NCT02413827
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Celldex Therapeutics
Industry
Enrollment
9 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
Apr 2015 (Actual)
Primary completion
Nov 2, 2016 (Actual)
Completion
Nov 9, 2016 (Actual)
Last update posted
Apr 7, 2017

2015 – 2016

United States locations

U.S. sites
8
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
California Pacific Medical Center Research Institute San Francisco California 94115 —
Sutter Pacific Medical Foundation Santa Rosa California 95403 —
University of Colorado Aurora Colorado 80045 —
Georgetown University School of Medicine Washington D.C. District of Columbia 20007 —
University of Chicago Chicago Illinois 60637 —
Washington University School of Medicine St Louis Missouri 63110 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15232 —
Tennessee Oncology Sarah Cannon Research Institute Nashville Tennessee 37203 —

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 NCT02413827, 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 Apr 7, 2017 · Synced Nov 15, 2026

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