ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Efficacy and Safety of Talimogene Laherparepvec Neoadjuvant Treatment Plus Surgery Versus Surgery Alone for Melanoma

ClinicalTrials.gov ID: NCT02211131

Public ClinicalTrials.gov record NCT02211131. 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 Apr 29, 2026, 12:38 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 2, Multicenter, Randomized, Open-label Trial Assessing the Efficacy and Safety of Talimogene Laherparepvec Neoadjuvant Treatment Plus Surgery Versus Surgery Alone for Resectable, Stage IIIB to IVM1a Melanoma

Study identification

NCT ID
NCT02211131
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Amgen
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

  • Immediate surgical resection of melanoma lesion(s) Procedure
  • Talimogene Laherparepvec Drug

Procedure · 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
Feb 2, 2015
Primary completion
Apr 29, 2019
Completion
Apr 27, 2022
Last update posted
Jun 4, 2023

2015 – 2022

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Research Site Birmingham Alabama 35249
Research Site Duarte California 91010
Research Site Orange California 92868
Research Site San Francisco California 94115
Research Site Santa Monica California 90404
Research Site Daytona Beach Florida 32117
Research Site Gainesville Florida 32610
Research Site Tampa Florida 33612
Research Site Louisville Kentucky 40202
Research Site Worcester Massachusetts 01655
Research Site Omaha Nebraska 68130
Research Site New Brunswick New Jersey 08903
Research Site New York New York 10029
Research Site New York New York 10032
Research Site Chapel Hill North Carolina 27599
Research Site Columbus Ohio 43210
Research Site Philadelphia Pennsylvania 19107
Research Site Memphis Tennessee 38163
Research Site Dallas Texas 75230
Research Site Dallas Texas 75390
Research Site Houston Texas 77030
Research Site Salt Lake City Utah 84112

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02211131, 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 Jun 4, 2023 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02211131 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →