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Clinical Trial Summary

To evaluate the efficacy and safety of tebentafusp-based regimens tebentafusp monotherapy and in combination with anti-PD1 vs investigator choice (including clinical trials of investigational agents, salvage therapy per local standard of care (SoC), best supportive care (BSC)) on protocol survivor follow up) in patients with advanced non-ocular melanoma


Clinical Trial Description

This is a Phase 2/3, multicenter, open-label study to evaluate the efficacy and safety of tebentafusp as monotherapy (Arm A) and in combination with pembrolizumab (Arm B) compared with standard of care or best supportive care (Arm C) in participants with non-ocular advanced melanoma who have progressed on a prior anti-PD(L)1 regimen, received prior ipilimumab and, if the participant has a BRAF mutation, a prior BRAF tyrosine kinase inhibitor (TKI) regimen. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05549297
Study type Interventional
Source Immunocore Ltd
Contact Immunocore Medical Information
Phone 844-466-8661
Email medical.information@immunocore.com
Status Recruiting
Phase Phase 2/Phase 3
Start date December 19, 2022
Completion date September 2027

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