Logo

F2G's Olorofim Receives the US FDA's Breakthrough Therapy Designation to Treat Invasive Mold Infections in Patients with Limited or No Treatment Options

Share this

F2G's Olorofim Receives the US FDA's Breakthrough Therapy Designation to Treat Invasive Mold Infections in Patients with Limited or No Treatment Options

Shots:

  • The BT designation follows the P-IIb Trial in patients with IFD or probable invasive aspergillosis (IA) and either refractory disease- resistance- or intolerance to available agents
  • The study resulted in well tolerable results across more than 10 years of patient dosing days with a median therapy duration of 12 wks.
  • Olorofim is first antifungal agent targeted to treat invasive fungal mold infections such as azole-resistant aspergillosis- scedosporiosis- lomentosporiosis- and other rare mold infections and is being developed as IV and oral formulation

Click here ­to­ read full press release/ article | Ref: PRNewswire  | Image: F2G


Senior Editor

This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions