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Regeneron’s Libtayo (cemiplimab) Receives EC’s Approval as the 2L Treatment of Recurrent or Metastatic Cervical Cancer

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Regeneron’s Libtayo (cemiplimab) Receives EC’s Approval as the 2L Treatment of Recurrent or Metastatic Cervical Cancer

Shots:

  • The EC has approved Libtayo as monotx. in adult patients with recurrent or metastatic cervical cancer & disease progression on or after Pt-based CT
  • The approval was based on the P-III (EMPOWER-Cervical 1) trial evaluating Libtayo (350mg, q3w) as monotx. vs CT in 608 patients across 14 countries irrespective of PD-L1 expression status or histology which showed an improvement in OS, PFS & ORR, 31% & 27% reduction in risk of death & a longer m-OS in the overall population & SCC histology (12.0 vs 8.5mos. & 11.1 vs 8.8mos.), 25% reduction of risk in progressive disease while ORR (16% vs 6%) in the overall population
  • Immune-mediated adverse reactions (21%), permanent discontinuation (4.6%) with no new Libtayo safety signals. The results were published in NEJM

Ref: Regeneron | Image: Regeneron

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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