Preetam Jain: FDA Approves Vepdegestrant For ESR1-Mutant HR+/HER2- MBC
Preetam Jain/ X

Preetam Jain: FDA Approves Vepdegestrant For ESR1-Mutant HR+/HER2- MBC

Preetam Jain, Consultant Medical Oncologist and Hemato-Oncologist at Bombay Hospital and Medical Research Centre, shared a post on X:

“Big News in Breast Cancer Treatment ​

The FDA has approved Vepdegestrant, a novel oral protein degrader for patients with ESR1-mutated ER+/HER2- metastatic breast cancer whose disease has progressed on prior endocrine therapy.

​This biomarker-defined approval highlights the critical importance of ESR1 mutation testing to guide treatment decisions. ​Data from the VERITAC-2 trial shows a significant improvement in median Progression-Free Survival (mPFS) of 5.0 months compared to 2.1 months with fulvestrant (HR: 0.57). ​An exciting new precision medicine option for our patients.”

Preetam Jain: FDA Approves Vepdegestrant For ESR1-Mutant HR+/HER2- MBC