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No Longer Available No phase listed Expanded access

Expanded Access Protocol of Talimogene Laherparepvec for Subjects With Unresected, Stage lllB to IVM1c Melanoma

ClinicalTrials.gov ID: NCT02147951

Public ClinicalTrials.gov record NCT02147951. 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 13, 2026, 8:22 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 3b, Multicenter, Open-label, Single-arm, Expanded Access Protocol of Talimogene Laherparepvec for the Treatment of Subjects With Unresected, Stage lllB to IVM1c Melanoma

Brief summary

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

Expanded access of Talimogene Laherparepvec for subjects with unresected, stage IIIb to IVM1c Melanoma.

Study identification

NCT ID
NCT02147951
Recruitment status
No Longer Available
Study type
Expanded access
Phase
Not listed
Lead sponsor
Amgen
Industry
Enrollment
Not listed

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 95 Years
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
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Feb 29, 2016

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
Research Site Mobile Alabama 36604
Research Site Mobile Alabama 36608
Research Site Little Rock Arkansas 72205
Research Site Duarte California 91010
Research Site La Jolla California 92093-0698
Research Site Daytona Beach Florida 32117
Research Site Jacksonville Florida 32207
Research Site Miami Beach Florida 33140
Research Site Indianapolis Indiana 46260
Research Site Louisville Kentucky 40202
Research Site Minneapolis Minnesota 55407
Research Site St Louis Missouri 63110-1093
Research Site Omaha Nebraska 68130
Research Site Omaha Nebraska 68198
Research Site Morristown New Jersey 07962
Research Site New York New York 10016
Research Site Winston-Salem North Carolina 27157
Research Site Canton Ohio 44718
Research Site Portland Oregon 97213
Research Site Greenville South Carolina 29605
Research Site Dallas Texas 75230
Research Site Dallas Texas 75390
Research Site Franklin Wisconsin 53132
Research Site Wauwatosa Wisconsin 53226

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 NCT02147951, 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 Feb 29, 2016 · Synced Sep 13, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02147951 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →