15.05.2024 16:00:14 - Press Release: Novartis highlights pioneering innovation in CML with data from Scemblix(R) Phase III ASC4FIRST study in newly diagnosed patients at ASCO and EHA

*DJ Novartis highlights pioneering innovation in CML with data from Scemblix(R) Phase III ASC4FIRST study in newly diagnosed patients at ASCO and EHA

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May 15, 2024 10:00 ET (14:00 GMT)

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-- Primary results of the Scemblix(R) ASC4FIRST pivotal Phase III study in
first-line Ph+ CML-CP supporting third US FDA Breakthrough Therapy
designation, to be detailed in the ASCO Press Program and the EHA Plenary
Session

-- Latest data from the Kisqali(R)* NATALEE trial, including efficacy
endpoints for patients with node-negative stage II and III HR+/HER2-
early breast cancer

-- New radioligand therapy portfolio data supporting overall platform
leadership and ongoing expansion in research infrastructure and supply
capabilities
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Basel, May 15, 2024 -- Novartis will present data from more than 60 abstracts, including investigator-initiated trials at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting and the European Hematology Association (EHA) 2024 Hybrid Congress. The primary results from ASC4FIRST, a pivotal Phase III study of Scemblix(R) (asciminib) versus standard of care tyrosine kinase inhibitors (imatinib, nilotinib, dasatinib, and bosutinib) in newly diagnosed patients with Philadelphia chromosome positive chronic myeloid leukemia in chronic phase (Ph+ CML-CP) will be shared at the ASCO official Press Program and at the EHA Plenary Session.

Despite progress, people with CML continue to struggle to find treatment that is both efficacious and tolerable for them at diagnosis and beyond. We look forward to sharing the primary analysis from the pivotal Phase III ASC4FIRST trial, which builds on our over 20-year legacy to transform care for people diagnosed with CML," said Jeff Legos, Executive Vice President, Global Head of Oncology, Novartis. "With these promising data, a new analysis of the NATALEE trial in patients with node-negative early breast cancer and additional updates from our RLT portfolio, we further our efforts to reimagine medicine for those with cancer in partnership with the scientific community."

Key highlights of data accepted by ASCO include:

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Medicine Abstract Title Abstract Number/
Presentation Details
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Scemblix                                                    ASC4FIRST, a pivotal phase 3 study of asciminib (ASC)        Abstract #LBA6500 
vs investigator-selected tyrosine kinase inhibitors          Oral presentation 
(IS TKIs) in newly diagnosed patients (pts) with chronic     Friday, May 31 
myeloid leukemia (CML): Primary results                      2:45 - 5:45pm CDT 
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Kisqali(R) (ribociclib)                                     Baseline (BL) characteristics and efficacy endpoints         Abstract #512 
for patients (pts) with node-negative (N0) HR+/HER2-         Rapid oral presentation 
early breast cancer (EBC): NATALEE trial                     Friday, May 31 

2:45 - 4:15pm CDT
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Kisqali                                                     On-treatment (tx) dynamic circulating tumor DNA changes      Abstract #1012 
( ctDNA) associated with progression-free survival           Clinical Science Symposium 
(PFS) and overall survival (OS) of patients (pts)            Sunday, June 2 
with HR+/HER2- advanced breast cancer (ABC) in MONALEESA-3   4:30 - 6:00pm CDT 

(ML-3)
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Kisqali                                                     Short-term risk of recurrence in patients (pts) with         Abstract #541 

HR+/HER2- early breast cancer (EBC) treated with endocrine Poster presentation therapy (ET) in randomized clinical trials (RCTs): Sunday, June 2
A meta-analysis 9:00am - 12:00pm CDT
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Kisqali                                                     Real-world (RW) risk recurrence among patients (pts)         Abstract #e12533 
diagnosed with stage II-III HR+/HER2- early breast           Online publication 

cancer (EBC) treated with endocrine therapy (ET) in
the US
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Pluvicto(TM) (INN: lutetium ((177) Lu) vipivotide           Health-related quality of life and pain in a phase           Abstract #5003 
tetraxetan / USAN: lutetium Lu 177 vipivotide tetraxetan)   3 study of [(177) Lu]Lu-PSMA-617 in taxane-naïve        Oral presentation 
patients with metastatic castration-resistant prostate       Saturday, June 1 
cancer (PSMAfore)                                            3:00 - 6:00pm CDT 
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Pluvicto                                                    Baseline ctDNA analyses and associations with outcomes       Abstract #5008 
in taxane-naive patients with mCRPC treated with (177)       Oral presentation 
Lu-PSMA-617 versus change of ARPI in PSMAfore                Saturday, June 1 

3:00 - 6:00pm CDT
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Pluvicto                                                    Real-world clinical outcomes and economic burden of          Abstract #e17043 
early discontinuation of taxane therapy among patients       Online publication 

with metastatic castration-resistant prostate cancer
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Pluvicto                                                    Patient characteristics, treatment patterns and early        Abstract #e17048 
trends of lutetium Lu 177 vipivotide tetraxetan ((177)       Online publication 

Lu-PSMA-617) use by US urologists and oncologists
----------------------------------------------------------  -----------------------------------------------------------  --------------------------- 
Lutathera(R) (INN: lutetium ((177) Lu) oxodotreotide        Safety and time to response of [(177) Lu]Lu-DOTATATE         Abstract #4131 
/ USAN: lutetium Lu 177 dotatate)                           in patients with newly diagnosed advanced grade 2            Poster presentation 
and grade 3, well-differentiated gastroenteropancreatic      Saturday, June 1 
neuroendocrine tumors: Sub-analysis of the phase 3           1:30 - 4:30pm CDT 

randomized NETTER-2 study
---------------------------------------------------------- ----------------------------------------------------------- ---------------------------

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At the ASCO Annual Meeting, Novartis will also address health equity at the company's booth on the meeting floor, with the More Than Just Words virtual reality experience. Meeting attendees will have the opportunity to immerse themselves in scenarios inspired by real-life microaggressions Black patients face due to bias in care, and explore resources co-created with leading multidisciplinary experts to help foster productive, nonbiased conversations about breast cancer risk, diagnosis, and care.

MORE TO FOLLOW) Dow Jones Newswires

May 15, 2024 10:00 ET (14:00 GMT)
Name WKN Börse Kurs Datum/Zeit Diff. Diff. % Geld Brief Erster Schluss
NOVARTIS NAM. SF 0,49 904278 Hamburg 0,000 25.06.24 21:13:52 ±0,000 ±0,00% 0,000 0,000 0,000 80,190
Novartis AG 907122 NYSE 107,195 25.06.24 20:58:11 +0,245 +0,23% 107,200 107,210 107,220 106,950

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