Logo

Novartis Terminates Clinical Development of Fevipiprant (AW039) in P-III LUSTER Studies for Patients with Uncontrolled GINA 4/5 Asthma

Share this

Novartis Terminates Clinical Development of Fevipiprant (AW039) in P-III LUSTER Studies for Patients with Uncontrolled GINA 4/5 Asthma

Shots:

  • The P-III LUSTER-1 & 2 studies involve assessing of Fevipiprant (150/ 450mg) vs PBO in 894 & 877 patients aged ≥12yrs. in a ratio (1:1:1) with moderate-severe asthma- receiving GINA 4 and 5 SoC asthma therapy for 52wks. respectively
  • The pooled analysis of P-III LUSTER 1 & 2 study did not support the further development of Fevipiprant for asthma as a primary indication- but it was well tolerated with AEs balanced across treatments groups
  • Fevipiprant (qd) is an investigational- steroid-free therapy- act by blocking the DP2 pathway. Additionally- Novartis continues to invest in respiratory therapies with its respiratory portfolio including Xolair- Ultibro Breezhaler- QVM149

Click here to­ read full press release/ article | Ref: Novartis | Image: StraitTimes


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