Phase 2 open-label, multicenter, single-arm study of cemiplimab in patients with locally advanced basal cell carcinoma after hedgehog inhibitor therapy: Extended follow-up - 11/01/24
, Aleksandar Sekulic, MD b, Ketty Peris, MD c, Oliver Bechter, MD d, Sorilla Prey, MD e, Karl D. Lewis, MD f, Nicole Basset-Seguin, PhD g, Anne Lynn S. Chang, MD h, Stéphane Dalle, MD i, Almudena Fernández Orland, MD j, Lisa Licitra, MD k, Caroline Robert, PhD l, Claas Ulrich, MD m, Axel Hauschild, MD n, Michael R. Migden, MD o, Reinhard Dummer, MD p, Suk-Young Yoo, PhD q, Emmanuel Okoye, MBBS, MPH q, Ioannis Bassukas, MD r, Carmen Loquai, MD s, Vincenzo De Giorgi, MD t, Zeynep Eroglu, MD u, Ralf Gutzmer, MD v, Jens Ulrich, MD w, Susana Puig, MD x, Timothy J. Inocencio, PharmD, PhD q, Chieh-I Chen, MPH q, Patrick R. LaFontaine, PharmD y, Frank Seebach, MD q, Israel Lowy, MD, PhD q, Matthew G. Fury, MD, PhD qKey words : cemiplimab, clinical trial, hedgehog inhibitor, immune checkpoint inhibitor, locally advanced basal cell carcinoma, phase 2, quality of life
| Funding sources: This study was funded by Regeneron Pharmaceuticals, Inc, and Sanofi. |
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| Patient consent: All patients provided written informed consent. |
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| IRB approval status: The study protocol and all amendments were approved by the institutional review board/ethics committee at each participating study site. |
Vol 90 - N° 2
P. 414-418 - février 2024 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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