Novartis receives FDA accelerated approval for Fabhalta® (iptacopan), the first and only complement inhibitor for the reduction of proteinuria in primary IgA nephropathy (IgAN)
arcticnovartis
Ad hoc announcement pursuant to Art. 53 LR
Novartis receives FDA accelerated approval for Fabhalta® (iptacopan), the first and only complement inhibitor for the reduction of proteinuria in primary IgA nephropathy (IgAN)
arcticnovartis
Ad hoc announcement pursuant to Art. 53 LR
Novartis Scemblix® granted FDA Priority Review for the treatment of adults with newly diagnosed CML
arcticnovartis
- Priority Review based on ASC4FIRST Phase III study with Scemblix® data first to show significantly improved molecular response and a favorable safety and tolerability profile compared to standard of care therapies (imatinib and 2G TKIs)1
- Treatment options combining high efficacy with safety and tolerability represent a critical gap in care for long-term CML management1
Novartis Scemblix® granted FDA Priority Review for the treatment of adults with newly diagnosed CML
arcticnovartis
- Priority Review based on ASC4FIRST Phase III study with Scemblix® data first to show significantly improved molecular response and a favorable safety and tolerability profile compared to standard of care therapies (imatinib and 2G TKIs)1
- Treatment options combining high efficacy with safety and tolerability represent a critical gap in care for long-term CML management1
Novartis erzielt im zweiten Quartal weiterhin kräftige Umsatzsteigerungen und erhöht die Kerngewinnmarge; Gewinnprognose für das Geschäftsjahr 2024 angehoben
arcticnovartis
Ad-hoc-Mitteilung gemäss Art. 53 KR
Novartis erzielt im zweiten Quartal weiterhin kräftige Umsatzsteigerungen und erhöht die Kerngewinnmarge; Gewinnprognose für das Geschäftsjahr 2024 angehoben
arcticnovartis
Ad-hoc-Mitteilung gemäss Art. 53 KR
ADDRESS
Suite 204, Block 1
Long Cheng Plaza
Mutley Bend, Belvedere
Harare, Zimbabwe
CALL US
+263 (242) 741 308
+263 (242) 741 309
Mon-Fri: 8am – 5pm
