Logo

Context Therapeutics’ Clinical Partner Stemline Therapeutics Receives the US FDA’s Approval of Orserdu (elacestrant) for ER+, HER2-, ESR1-Mutated Breast Cancer

Share this
Context Therapeutics

Context Therapeutics’ Clinical Partner Stemline Therapeutics Receives the US FDA’s Approval of Orserdu (elacestrant) for ER+, HER2-, ESR1-Mutated Breast Cancer

Shots:

  • The US FDA has approved Orserdu for postmenopausal women or adult men with ER+, HER2-, ESR1-mutated advanced or metastatic breast cancer. The approval was based on the P-III trial (EMERALD) results evaluating elacestrant vs SoC endocrine monotx. in 478 patients
  • The trial met both 1EPs in all patients & whose tumors harbor ESR1 mutations (45% reduction in risk of progression or death) along with a significant PFS, m-PFS (8.6 vs 1.9mos.) whose tumors harbored ESR1 mutations & had been treated with a CDK4/6i for 12mos.
  • ONA-XR (onapristone extended release), an oral progesterone receptor antagonist is being tested in the ongoing P-Ib/II trial (ELONA) to improve the activity of Orserdu in ESR1-mutated & wild-type metastatic breast cancer

Ref: GlobeNewswire | Image: Context Therapeutics

Related News:- Context and Menarini Entered into a Clinical Trial Collaboration and Supply Agreement to Evaluate ONA-XR + Elacestrant for Metastatic Breast Cancer

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.

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions