CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 44 enrolled
Drug / intervention
High-dose IL-2 +1 moredrug
Likely dose
High-dose IL-2 600,000 IUfrom 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/NCT01416831
NCT01416831Phase 2Active

Phase II Randomized Study of High Dose Interleukin-2 Versus Stereotactic Body Radiation (SBRT) and High Dose Interleukin-2 (IL-2) in Patients With Metastatic Melanoma

Providence Health & Services·interventional·Posted Aug 15, 2011·Updated Apr 24, 2026

In Brief

A Phase 2 clinical trial evaluating Radiation therapy and high-dose IL-2 and High-dose IL-2 for Metastatic Melanoma. Active but no longer recruiting, targeting 44 participants across 1 site.

Detailed Summary

The purpose of this study is compare the response rates in patients with metastatic melanoma treated with high-dose IL-2 to patients treated with high-dose IL-2 along with radiation therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2Active
2012201320142015201620172018201920202021202220232024202520262027
First PostedAug 15, 2011
Enrollment StartJul 1, 2011
Primary CompletionApr 5, 2017
Study CompletionDec 1, 2026
TodayJul 2, 2026
Enrollment to primary: 5.8 yearsPosted 14.9 years ago

Interventions

Radiation therapy and high-dose IL-2other

Patients 1 - 20 will receive a single fraction of radiation. Patients 21 through the completion of the study will receive two fractions. The dose for all patients will be 20 Gy per fraction to the prescription line at the edge of the planning treatment volume (PTV) with the last dose delivered on a Friday before IL-2 administration. For patients receiving two radiation doses, the doses can be administered on the Wednesday and Friday before IL-2 starts. Patients who are assigned to IL-2 monotherapy and have progressive disease after two IL-2 cycles are then eligible to receive SBRT before cycle 3 of IL-2 commences, single fraction for patients 1-20 and two fractions for patients 21- end of study.

High-dose IL-2drug

IL-2 will be given on a Monday at a dose of 600,000 IU per kilogram IV every 8 hours for up to 14 doses each cycle. The second cycle is planned 16 days after cycle 1 but may be delayed up to one week to allow toxicity to resolve. The maximum number of doses that can be given during two cycles will be 28 doses. Patients who respond after two cycles can receive 4 more cycles of IL-2. Patients with disease progression after 2 cycles may elect to receive radiation before a 3rd cycle of IL-2. If patients crossover, IL-2 will be given on the Monday following the last dose of radiation, at a dose of 600,000 IU per kilogram IV every 8 hours for a maximum of 14 doses each cycle. Another cycle is planned 16 days after cycle 3 but may be delayed up to one week to allow toxicity to resolve.