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Clinical Trial Summary

Background - Advanced cutaneous T-cell lymphoma (mycosis fungoides, MF) is an incurable extranodal mature lymphoma with poor prognosis. Currently available therapies provide only short-term remissions. Rationale - MF is an immunogenic cancer and expresses a high number of neoantigens. therefore it it reasonable to assume that it would respond to immune checkpoint inhibitors. Objectives - The primary objective is to test the clinical efficacy (objective response rate) of the immune checkpoint inhibitor cemiplimab in patients with advanced mycosis fungoides (MF) who failed first-line therapy, defined as the sum of complete and partial responses (where at least 50% reduction of mSWAT is achieved).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05538988
Study type Interventional
Source AHS Cancer Control Alberta
Contact
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date December 2024
Completion date March 2026

See also
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Completed NCT02883517 - Cell-free Circulating DNA in Primary Cutaneous Lymphomas
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