Myovant Sciences Ltd and Pfizer Inc Receive FDA Approval for MYFEMBREE® Transcript
Good day, everyone, and welcome to Myovant Sciences MYFEMBREE FDA approval conference call. Today's call is being recorded.
At this time, I would like to turn the call over to Ryan Crowe, Vice President of Investor Relations at Myovant. Please go ahead.
Thank you, operator. Good morning, and thank you for joining us today to discuss the FDA approval of MYFEMBREE for the management of heavy menstrual bleeding associated with uterine fibroids in premenopausal women. Our press release as well as the slides that will be presented today are available on our Investor Relations website, investors.myovant.com.
Joining me for today's call are Dave Marek, Myovant's Chief Executive Officer; Frank Karbe, President and Chief Financial Officer; Lauren Merendino, Chief Commercial Officer; and Dr. Juan Camilo Arjona, Chief Medical Officer.
During the course of this conference call, we'll be making forward-looking statements. These include plans and expectations with respect to our products, product
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