A Phase 2 interventional study of anti-OX40 in Metastatic Melanoma, sponsored by Providence Health & Services. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-03-07.
Sponsored by Providence Health & Services · Phase 2, Interventional, and Treatment
In this study, anti-OX40 will be given to patients with melanoma to find out how the immune system responds to treatment with anti-OX40. It is hoped that this treatment will cause an immune response against melanoma resulting in tumor regression, but this is not known at this time. Anti-OX40 is a large protein that can help immune cells that fight bacteria, viruses and cancer cells.
3,006 studies on the registry are indexed under Melanoma; 520 are open to participants now.
Browse Melanoma studies →Providence Health & Services is the lead sponsor of 83 studies on the registry; 6 are open to participants now.
Of its 10 completed or terminated interventional studies of FDA-regulated products, 8 (80%) have results posted.
Counted across the registry records on this site, refreshed daily.
Laboratory values (performed within 28 days prior to enrollment) as follows:
Exclusion Criteria:
Patients with metastatic melanoma will be given 0.4 mg/kg anti-OX40 on days 1, 3 and 5 of a single treatment cycle.
Increased number of tumor antigen specific circulating T Cells
T Cells will be harvested by apheresis at baseline and Day 15 following anti-OX40 administration.
Time frame: Screening (baseline) and Day 15
This study is withdrawn, as verified in Mar 2013. You cannot join it, but the record below documents what was studied.
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Providence Health & Services