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Completed Phase 2 Interventional

Anti-Tumor Activity Of SB-485232 In Patients With Previously Untreated Metastatic Melanoma

ClinicalTrials.gov ID: NCT00107718

Public ClinicalTrials.gov record NCT00107718. 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 Oct 20, 2026, 12:38 AM 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 II Study of IL-18 in Melanoma Patients

Brief summary

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

This Phase II study is designed to evaluate the anti-tumor activity of three dose groups of SB-485232 (0.01, 0.1, and 1.0 mg/kg/day) administered intravenously as a single agent in subjects with previously untreated metastatic melanoma.

Study identification

NCT ID
NCT00107718
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
64 participants

Conditions and interventions

Conditions

Interventions

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
Nov 15, 2004 (Actual)
Primary completion
May 19, 2006 (Actual)
Completion
May 19, 2006 (Actual)
Last update posted
Jul 27, 2017

2004 – 2006

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
GSK Investigational Site Los Angeles California 90089 —
GSK Investigational Site San Francisco California 94115 —
GSK Investigational Site Santa Monica California 90404-2104 —
GSK Investigational Site New Haven Connecticut 06520 —
GSK Investigational Site Jacksonville Florida 32209 —
GSK Investigational Site Miami Beach Florida 33140 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Indianapolis Indiana 46202 —
GSK Investigational Site Lutherville-Timonium Maryland 21093 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site Toledo Ohio 43614-5809 —
GSK Investigational Site Pittsburgh Pennsylvania 15213-2584 —

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 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00107718, 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 Jul 27, 2017 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00107718 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →