Novartis malaria treatment Coartem® Baby receives WHO prequalification, paving way for greater access for newborns and young infants
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  • Coartem® (artemether-lumefantrine) Baby is the first and only malaria treatment for newborns and young infants, closing long-standing treatment gap
  • WHO prequalification key milestone for donor-funded and public sector purchasing by UN and other procurement agencies
  • Novartis making treatment available on largely not-for-profit basis in areas where malaria is endemic

Novartis malaria treatment Coartem® Baby receives WHO prequalification, paving way for greater access for newborns and young infants
arcticnovartis

  • Coartem® (artemether-lumefantrine) Baby is the first and only malaria treatment for newborns and young infants, closing long-standing treatment gap
  • WHO prequalification key milestone for donor-funded and public sector purchasing by UN and other procurement agencies
  • Novartis making treatment available on largely not-for-profit basis in areas where malaria is endemic

Novartis announces expansion of community health programs to close gaps in heart disease and cancer care, targeting more than 30 countries by 2030
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  • Strengthens three community health models spanning community‑embedded care, earlier intervention and data‑driven population health

  • Scales program footprint from 11 countries to more than 30 by 2030, including across five cities in the U.S.

  • Builds on pilot programs that demonstrated significant increase in control rates for high blood pressure in pilot settings

Working with communities to close gaps in heart disease and cancer care
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Novartis IgAN data in New England Journal of Medicine show Fabhalta® slowed kidney function decline by 49.3%
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  • Fabhalta lowered likelihood of progression to kidney failure by 43% in APPLAUSE-IgAN study1
  • 40.7% of patients on Fabhalta demonstrated sustained reduction of protein in urine over two years1
  • Fabhalta granted priority review by FDA for traditional approval

Basel, March 29, 2026 – Novartis today announced final two-year results from the Phase III APPLAUSE‑IgAN study of Fabhalta® (iptacopan) in IgA nephropathy (IgAN).

Novartis withdraws EMA application for adding new indication for Pluvicto®
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