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FDA Grants Fast Track Designation in HR+/HER2- Metastatic Breast Cancer

The FDA granted Fast Track designation to gedatolisib for the treatment of HR+/HER2- metastatic breast cancer, following progression on CDK4/6 therapy, according to a press release.

The manufacturer anticipates FDA feedback in the first quarter of 2022 to finalize plans for the Phase 3 clinical trial. 

Additionally, the manufacturer will initiate two Phase 2 clinical trials for gedatolisib in patients with HR+/HER- breast cancer selected with a CELsignia P13K Pathway Test.

One trial will evaluate gedatolisib in combination with fulvestrant, and the second, will evaluate the treatment in combination with palbociclib and letrozole.

"Initiating clinical trials to evaluate gedatolisib in CELsignia selected patients in parallel with other CELsignia studies is very synergistic. First, we believe this will enhance the enrollment activities for each study. Secondly, these studies provide an efficient opportunity for Celcuity to evaluate gedatolisib in CELsignia PI3K test selected patients,” Brian Sullivan, CEO and co-founder of Celcuity, said in the release.

Reference:
https://www.accesswire.com/684239/Celcuity-Receives-FDA-Fast-Track-Designation-for-Gedatolisib-in-HR-HER2-Metastatic-Breast-Cancer-and-Provides-Corporate-Update

Images: Getty Images, Pixabay

By MD /alert Staff

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