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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 Nov 4, 2026, 12:43 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. 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
Mar 1, 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 Mar 1, 2016 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02147951 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →