The IgA Nephropathy Foundation转发了
“As a parent of a son living with the disease for 20 years, I understand firsthand the fear and uncertainty that come with an IgAN diagnosis, and the devastating impact it can have on patients and their families,” said Bonnie Schneider, Director and Co-Founder, IgAN Foundation. “Today’s approval offers new hope for people living with IgA nephropathy as it represents a treatment innovation that provides us with a new way to fight this multifaceted disease.” Read the full press release https://lnkd.in/eaTs_z5G #iganephropathy #thefutureisbright
This is amazing! Absolutely love seeing new options for IGAN patients!!
Key Account Director | Health Systems | Accomplished Strategic Accounts Leader | Driving Revenue Growth & Market Penetration | Rare Disease | Oncology | Hematology | Orphan Drugs Specialist | Sales | Market Access
3 个月This is fantastic news for this patient population. As a renal dialysis nurse I watched patients suffer for many years and now they have this option... So great for patients...