Fabhalta (iptacopan) — NDA/BLA submission
2026
Full data will be presented at future medical meetings and included in regulatory submissions in 2026.Source filing
NOVARTIS AG · Data as of 2026-09-08
2026
Full data will be presented at future medical meetings and included in regulatory submissions in 2026.Source filing
2026
Full study readout and submission for the remaining two subtypes of CINDU expected in 2026.Source filing
H2 2026
Del-desiran is currently being evaluated in the Phase III HARBOR study in DM1, with readout anticipated in H2 2026.Source filing
2027
Data presented at ASH, simultaneously published in NEJM, and will be included in regulatory submissions in 2027.Source filing
H1 2027
Zigakibart is currently being evaluated in the Phase III BEYOND study in adults with IgAN, with readout anticipated in H1 2027.Source filing
Oct 21–Oct 23
Novartis will present the REMODEL-1 and REMODEL-2 data as a late-breaker at MSToronto2026 and intends to host an investor call following the congress presentation.Source filing