Logo

Pfizer's Ibrance (palbociclib) Fails to Meet its Primary Endpoint in P-lll PENELOPE-B Study for Early Breast Cancer

Share this

Pfizer's Ibrance (palbociclib) Fails to Meet its Primary Endpoint in P-lll PENELOPE-B Study for Early Breast Cancer

Shots:

  • The P-lll PENELOPE-B study involves the assessment of Ibrance vs PBO in addition to at least 5yrs. of standard adjuvant endocrine therapy in 1-250 women with HR+- HER2- eBC at high risk of recurrence who have the residual invasive disease after completing neoadjuvant CT
  • The study did not meet its 1EPs of (iDFS) in women with eBC- no unexpected safety signals were observed. The trial is sponsored by the GBG as part of a clinical research collaboration with Pfizer and other study groups
  • Ibrance is an oral inhibitor of CDKs 4 and 6 and is approved in 95+ countries and has been prescribed to ~340-000 patients globally

    ­ Ref: Pfizer | Image: TrialSite News

 

Click here to­ read the full press release 

Senior Editor

This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions