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08:56:46 EDT Fri 03 May 2024
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Z:NVS - NOVARTIS AG ADR-EACH REPR 1 CHF0.5(REGD) - http://www.novartis.com
Sym-XBid - AskLastChg%ChVol$Vol#TrOpen-Hi-LoYear Hi-LoLast TrNewsDelay
NVS - Z0.498.12·98.170.897.3416.81,64367    108.78  92.1908:37:47Apr 1515 min RT 2¢

Recent Trades - Last 10 of 67
Time ETExPriceChangeVolume
08:37:47Z98.130.79400
08:37:47Z98.130.79400
08:37:47Z98.130.79200
08:37:38Z98.100.76800
08:37:38Z98.100.76200
08:37:25Z98.140.80200
08:37:25Z98.140.80100
08:37:25Z98.150.81200
08:37:06Z98.1760.8361
08:37:06Z98.1760.83668

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Recent Bulletins
Date ETSymbolTypeHeadline
2024-04-15 14:00U:NVSNews ReleaseNew Novartis Fabhalta(TM) (iptacopan) data show clinically meaningful and statistically significant proteinuria reduction of 38.3% versus placebo for patients with IgA nephropathy (IgAN)
2024-04-11 07:01U:NVSNews ReleaseArvinas Enters into a Transaction with Novartis, including a Global License Agreement for the Development and Commercialization of PROTAC(TM) Androgen Receptor (AR) Protein Degrader ARV-766 for the Treatment of Prostate Cancer
2024-04-06 16:16U:NVSNews ReleaseNew Novartis data show early addition of twice-yearly* Leqvio(TM) (inclisiran) following maximally tolerated statin therapy significantly reduces LDL-C in ASCVD patients in real-world setting
2024-02-14 08:00U:NVSNews ReleaseErasca Announces Two Clinical Trial Collaboration and Supply Agreements for Trametinib to Evaluate Naporafenib Combination in SEACRAFT-1 and SEACRAFT-2 Trials
2023-12-10 19:39U:NVSNews ReleaseNovartis presents new 48-week results from Phase III APPLY-PNH trial showing sustained efficacy and long-term safety of Fabhalta ‚ ® (iptacopan) in adults with paroxysmal nocturnal hemoglobinuria (PNH)
2023-12-06 00:18U:NVSNews ReleaseNovartis receives FDA approval for Fabhalta ‚ ® (iptacopan), offering superior hemoglobin improvement in the absence of transfusions as the first oral monotherapy for adults with PNH
2023-09-11 10:00U:NVSNews ReleaseNovartis Issues Voluntary Nationwide Recall of One Lot of Sandimmune ‚ ® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL due to Crystallization
2023-06-08 07:00U:NVSNews ReleaseKAZIA THERAPEUTICS ANNOUNCES PHASE II CLINICAL STUDY TO INVESTIGATE PAXALISIB IN RECURRENT/PROGRESSIVE IDH-MUTANT GRADE 2 & 3 GLIOMA