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Sanofi: Libtayo (cemiplimab) approved by the European Commission for first-line treatment of patients with advanced non-small cell lung cancer with =50% PD-L1 expression

Libtayo (cemiplimab) approved by the European Commission for first-line treatment of patients with advanced non-small cell lung cancer with =50% PD-L1 expression Approval ....

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Regeneron Pharmaceuticals : Libtayo® (cemiplimab) Approved by the European Commission for First-Line Treatment of Patients with Advanced Non-small Cell Lung Cancer with ≥50% PD-L1 Expression

TARRYTOWN, N.Y. and PARIS, June 25, 2021 /PRNewswire/
Approval based on a Phase 3 trial demonstrating Libtayo significantly improved overall survival compared to chemotherapy in advanced. | June 25, 2021 ....

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Regeneron Pharmaceuticals : Libtayo® (cemiplimab) Approved by the European Commission as the First Immunotherapy Indicated for Patients with Advanced Basal Cell Carcinoma

TARRYTOWN, N.Y. and PARIS, June 25, 2021 /PRNewswire/
Approval based on data from the largest trial to date in patients with advanced basal cell carcinoma previously treated with a hedgehog pathway inhibitor
Libtayo now approved by the European Commission for three advanced cancers
Regeneron Pharmaceuticals, Inc. (NASDAQ:
REGN) and Sanofi today announced that the European Commission (EC) has approved the PD-1 inhibitor Libtayo
® (cemiplimab) to treat adults with locally advanced or metastatic basal cell carcinoma (BCC) who have progressed on or are intolerant to a hedgehog pathway inhibitor (HHI).
BCC is the most common type of skin cancer worldwide, representing up to 80% of non-melanoma skin cancers, and incidence is increasing across many European countries. While the large majority of BCCs are caught early and easily cured with surgery and/or radiation, a small proportion of cases can develop into advanced BCC and penetrate deeper into surround ....

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Sanofi: Libtayo® (cemiplimab) approved by the European Commission as the first immunotherapy ...

Press release content from Globe Newswire. The AP news staff was not involved in its creation. ....

United States , France General , Kaplan Meier , Eva Schaefer Jansen , Arnaud Delepine , Suzanne Greco , Felix Lauscher , Vesna Tosic , Fara Berkowitz , Peterc Adamson , Ashleigh Koss , Natalie Pham , Taylor Ramsey , Regeneron Genetics Center , European Union , European Commission , Drug Administration , Clinical Sciences , Global Development Head , Israel Lowy , Senior Vice President , Nonproprietary Naming , Biological Products Guidance , Relations Contacts , North America , Media Relations Contact ,

Libtayo® (cemiplimab) Approved by the European Commission as the First Immunotherapy Indicated for Patients with Advanced Basal Cell Carcinoma

Press release content from PR Newswire. The AP news staff was not involved in its creation.
Libtayo® (cemiplimab) Approved by the European Commission as the First Immunotherapy Indicated for Patients with Advanced Basal Cell Carcinoma
June 25, 2021 GMT
TARRYTOWN, N.Y. and PARIS, June 25, 2021 /PRNewswire/
Approval based on data from the largest trial to date in patients with advanced basal cell carcinoma previously treated with a hedgehog pathway inhibitor
Libtayo now approved by the European Commission for three advanced cancers
Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Sanofi today announced that the European Commission (EC) has approved the PD-1 inhibitor Libtayo® (cemiplimab) to treat adults with locally advanced or metastatic basal cell carcinoma (BCC) who have progressed on or are intolerant to a hedgehog pathway inhibitor (HHI). ....

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