Novartis’ Newly Acquired Atrsentan P-III (ALIGN) Study Shows Positive Interim Results in IgA Nephropathy
Shots:
- Novartis plans to submit these 36wks. interim results for accelerated approval from FDA, where Atrasentan showed a reduction in proteinuria vs PBO in IgA Nephropathy patients
- The P-III (ALIGN) study is planned to continue for up to 136wks. in order to assess eGFR with confirmatory results expected by Q1’26
- Novartis recently acquired Chinook for Atresentan & Zigabikart (SC) both of which are under P-III clinical evaluation in IgAN patients. Additionally, the company recently published results for its organic Iptacopan (Factor B inhibitor) in IgAN patients
Ref: Novartis| Image: Novartis
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Shivani was a content writer at PharmaShots. She has a keen interest in recent innovations in the life sciences industry. She was covering news related to Product approvals, clinical trial results, and updates. We can be contacted at connect@pharmashots.com.
