Pfizer and Arvinas’ jointly develop oral treatment for breast cancer

Vepdegestrant is a novel oral PROteolysis Targeting Chimera (PROTAC) ER degrader specifically for estrogen receptor-positive and HER2-negative metastatic breast cancer previously treated by endocrine-based therapy that is being jointly developed by Arvinas and Pfizer.

Being developed jointly by Arvinas and Pfizer, the drug candidate is a heterobifunctional PROTAC (proteolysis-targeting chimera) and selective estrogen receptor degrader (SERD) acts by targeting estrogen receptor alpha and cereblon (CRBN).

Vepdegestrant is a novel oral PROteolysis Targeting Chimera (PROTAC) ER degrader that is being jointly developed by Arvinas and Pfizer.

Chairperson, CEO, and president of Arvinas, John Houston, said: “We are focused on the persisting unmet needs of people with ER+/HER2- breast cancer and doing all that we can to expedite the development of vepdegestrant as a novel, oral ER-targeted potential therapy for this patient community,”

“We are pleased the FDA has granted Fast Track designation for vepdegestrant, and we continue to believe this investigational drug has the potential to harness the body’s own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins.”

As described by the FDA, ‘fast track is a process designed to facilitate the development and expedite the review of drugs to treat serious conditions and fill an unmet medical need’.

Arvinas’ John Houston

The purpose is to get important new drugs to patients earlier. Vepdegestrant as a monotherapy is being studied in the ongoing Phase 3 VERITAC-2​ clinical trial, which is evaluating vepdegestrant or fulvestrant in patients with locally advanced or metastatic ER+/HER2- breast cancer who have been previously treated with an endocrine-based therapy.

Leave a Reply

Your email address will not be published. Required fields are marked *