CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 245 enrolled / 245 target
Drug / intervention
Ipilimumab +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01134614
NCT01134614Phase 2ActiveUpdate Overdue (1.3/mo)Completion was 160mo ago

A Phase II Trial of GM-CSF Protein Plus Ipilimumab in Patients With Advanced Melanoma

National Cancer Institute (NCI)·interventional·Posted Jun 2, 2010·Updated Jun 15, 2026

In Brief

A Phase 2 clinical trial evaluating Ipilimumab and Sargramostim for Advanced Melanoma and 8 related conditions. Active but no longer recruiting, targeting 245 participants across 257 sites.

Signals

Enrollment appears stalled

Detailed Summary

This randomized phase II trial is studying how well giving ipilimumab with or without sargramostim (GM-CSF) works in treating patients with stage III or stage IV melanoma that cannot be removed by surgery (unresectable). Ipilimumab works by activating the patient's immune system to fight cancer. Colony-stimulating factors, such as sargramostim, may increase the number of immune cells found in bone marrow or peripheral blood and may help the immune system recover from the side effects of treatment. It is not yet known whether giving ipilimumab together with sargramostim is more effective than ipilimumab alone in treating melanoma.

Study Details

Timeline

Phase 2Active
201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 2, 2010
Enrollment StartDec 28, 2010
Primary CompletionFeb 15, 2013
Study CompletionMar 19, 2027
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 16.1 years ago

Arms & Interventions

Arm A (ipilimumab and sargramostim)experimental

Patients receive induction therapy comprising ipilimumab IV over 90 minutes on day 1 and sargramostim SC once daily on days 1-14. Treatment repeats every 21 days for 4 cycles. After 12 weeks of induction treatment, anti-tumor response is assessed and patients then receive maintenance therapy comprising ipilimumab IV over 90 minutes on day 1 and sargramostim SC once daily on days 1-14. Treatment with ipilimumab repeats every 12 weeks and treatment with sargramostim repeats every 21 days. After 12 weeks of maintenance therapy, anti-tumor response is reassessed and patients with responsive or stable disease then continue maintenance therapy until disease progression or unacceptable toxicity.

Biological: IpilimumabBiological: Sargramostim
Arm B (ipilimumab)active_comparator

Patients receive induction therapy comprising ipilimumab IV over 90 minutes on day 1. Treatment repeats every 21 days for 4 cycles. After 12 weeks of induction treatment, anti-tumor response is assessed and patients then receive maintenance therapy of ipilimumab IV over 90 minutes on day 1. Treatment with ipilimumab repeats every 12 weeks. After 12 weeks of maintenance therapy, anti-tumor response is reassessed and cycles repeat every 12 weeks in the absence of disease progression or unacceptable toxicity

Biological: Ipilimumab

Interventions

Ipilimumabbiological

Given IV

Sargramostimbiological

Given SC