UNITED STATES
SECURITIES AND
EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM 6-K
REPORT OF FOREIGN
PRIVATE ISSUER
PURSUANT TO
RULE 13a-16 or 15d-16 OF
THE SECURITIES
EXCHANGE ACT OF 1934
Report on Form
6-K dated December 5, 2022
(Commission
File No. 1-15024)
____________________
Novartis AG
(Name of Registrant)
Lichtstrasse
35
4056 Basel
Switzerland
(Address of Principal
Executive Offices)
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Indicate by check mark whether the
registrant files or will file annual reports under cover of Form 20-F or Form 40-F:
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is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1):
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registrant by furnishing the information contained in this form is also thereby furnishing the information to the Commission pursuant
to Rule 12g3-2(b) under the Securities Exchange Act of 1934.
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Novartis International AG Novartis Global
Communications CH-4002 Basel Switzerland
https://www.novartis.com
https://twitter.com/novartisnews |
MEDIA & INVESTOR RELEASE
Novartis PluvictoTM
shows statistically significant and clinically meaningful radiographic progression-free survival benefit in patients with PSMA–positive
metastatic castration-resistant prostate cancer
Ad hoc announcement pursuant to Art. 53 LR
• |
Phase III PSMAfore trial with PluvictoTM met the primary endpoint of radiographic progression-free
survival (rPFS) in PSMA–positive mCRPC who have been treated with androgen-receptor pathway inhibitor (ARPI) therapy1 |
• |
Pluvicto becomes the first PSMA-targeted radioligand therapy to demonstrate clinical benefit in mCRPC
patients before receiving taxane-based chemotherapy1, addressing a significant unmet need2 |
• |
Findings to be presented at an upcoming medical meeting and submitted to regulatory authorities for approval
in 2023 |
• |
Novartis is advancing a broad portfolio of radioligand therapies to treat cancer and is investing in
manufacturing capacity to meet the growing global demand for treatment |
Basel, December 5, 2022 — Today, Novartis announced the pivotal Phase
III PSMAfore study with PluvictoTM (INN: lutetium (177Lu)
vipivotide tetraxetan), a prostate-specific membrane antigen (PSMA)-targeted radioligand therapy, met its primary endpoint. Pluvicto demonstrated
a statistically significant and clinically meaningful improvement in radiographic progression-free survival (rPFS) in patients with PSMA–positive
metastatic castration- resistant prostate cancer (mCRPC) after treatment with androgen-receptor pathway inhibitor (ARPI) therapy, compared
to a change in ARPI1. No unexpected safety findings were observed in PSMAfore; data are
consistent with the already-well established safety profile of Pluvicto1,3.
This is the second positive read-out for Pluvicto in a Phase III trial following
the VISION study, where patients with PSMA–positive mCRPC who received Pluvicto plus standard of care after being treated with ARPI
and taxane-based chemotherapy had a statistically significant reduction in risk of death1,3.
The PSMAfore results continue to support the important role of Pluvicto1 in treating patients
with prostate cancer. The Phase III data will be presented at an upcoming medical meeting and discussed with the US Food and Drug Administration
(FDA) in 2023 for regulatory approval.
“With the announcement of these positive topline Phase III results, Pluvicto
becomes the first PSMA-targeted radioligand therapy to demonstrate significant and clinically meaningful benefits for people living with
this type of prostate cancer who have not received taxane- based chemotherapy,” said Shreeram Aradhye, M.D., President, Global Drug
Development and Chief Medical Officer, Novartis. “We look forward to discussing the data with healthcare authorities in order to
bring this innovative new early treatment option to many more prostate cancer patients sooner after their diagnosis.”
The vast majority of patients diagnosed with CRPC already present with metastases
at time of diagnosis4, patients with metastatic prostate cancer have an approximate 3
in 10 chance of surviving 5 years5. Despite recent advances, outcomes for those who progress
after standard of care second-generation ARPI remain poor, and there is an urgent need for new targeted treatment options to help improve
long-term outcomes6,7,8,9.
Pluvicto is already approved for treatment in adult patients with PSMA–positive
mCRPC who have been treated with ARPI and taxane-based chemotherapy in the United States and several other countries10-12.
About the PSMAfore Study
PSMAfore is a Phase III, open-label, multi-center, 1:1 randomized study comparing
the efficacy and safety of Pluvicto to a change in ARPI in patients with PSMA–positive mCRPC13.
Patients enrolled must have progressed only once after receiving a second-generation ARPI13.
There were 469 participants enrolled in the study13. The primary endpoint is rPFS, defined
as the time from randomization to radiographic progression by PCWG3-modified RECIST v1.1 (as assessed by blinded independent central review)
or death13. Evaluation of overall survival, the key secondary endpoint, is ongoing as
data remain immature.
About PluvictoTM (lutetium (177Lu) vipivotide
tetraxetan)
Pluvicto is an intravenous radioligand therapy combining a targeting compound (a
ligand) with a therapeutic radionuclide (a radioactive particle, in this case lutetium-177)3.
After administration into the bloodstream, Pluvicto binds to target cells, including prostate cancer cells that express PSMA, a transmembrane
protein3. Once bound, energy emissions from the radioisotope damage the target cells and
nearby cells, disrupting their ability to replicate and/or triggering cell death10.
Pluvicto is approved in the US and other countries to treat adults with a type
of advanced cancer called PSMA–positive mCRPC and who have already been treated with other anticancer treatments (ARPI and taxane-based
chemotherapy)10-12. More specifically, in March 2022, the United States Food and Drug
Administration (US FDA) approved Pluvicto10. In August and September 2022, the Medicines
and Healthcare products Regulatory Agency (MHRA) and Health Canada approved Pluvicto in Great Britain and Canada, respectively11,12.
In October 2022, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion
recommending the granting of a marketing authorization for Pluvicto14. These regulatory
decisions are supported by the results from the pivotal Phase III VISION study, where patients with pre-treated PSMA– positive mCRPC
who received Pluvicto plus standard of care had a statistically significant reduction in the risk of death; both alternate primary endpoints
of radiographic progression free survival and overall survival were met3.
Novartis is also evaluating opportunities to investigate Pluvicto radioligand therapy
in earlier stages of prostate cancer15.
Novartis and Prostate Cancer
With more than 1.4 million new cases and 375,000 deaths in 2020 alone, prostate
cancer is the most frequently diagnosed cancer in men in 112 countries—more than half the world16.
At Novartis, we are harnessing the innovation of our world-class scientists, strategic
partnerships, and one of the industry’s most competitive pipelines to explore the potential of new, targeted therapies and precision
medicine platforms to address the greatest unmet needs in prostate cancer.
Through the bold science of targeted therapies, our goal is to reduce the global
disease burden, extend the lives of patients with prostate cancer, and elevate current standards of care.
Novartis and Radioligand Therapy (RLT)
Novartis is reimagining cancer care with radioligand therapy for patients with
advanced cancers. By harnessing the power of radioactive atoms and applying it to advanced cancers, RLT is theoretically able to deliver
radiation to target cells anywhere in the body17,18. Novartis has established global expertise,
specialized supply chain and manufacturing capabilities across its network of radioligand therapy production sites. In order to support
growing demand for our RLT platform, we are investing in the expansion of our RLT production capabilities in Millburn, New Jersey (US),
Zaragosa (Spain) and Ivrea (Italy), as well as building a new radioligand manufacturing facility in Indianapolis, Indiana (US), that is
planned to be operational in 2023. We are continually evaluating additional opportunities to expand capacity.
About Phenotypic Precision Medicine in Advanced Prostate Cancer
Despite advances in prostate cancer care, there is a high unmet need for new targeted
treatment options to improve outcomes for patients with mCRPC2. More than 80% of patients
with prostate cancer highly express a phenotypic biomarker called prostate specific membrane antigen (PSMA)19-23,
making it a promising diagnostic (through positron emission tomography (PET) scan imaging) and therapeutic target for radioligand therapy24.
This differs from ‘genotypic’ precision medicine which targets specific genetic alterations in cancer cells25.
Disclaimer
This press release contains forward-looking
statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements can generally
be identified by words such as “potential,” “will,” “may,” “could,” “look forward,”
“pipeline,” “to be presented,” “upcoming” “ongoing,” “evaluating,” “to
investigate,” “to address,” “continue,” or similar terms, or by express or implied discussions regarding
potential marketing approvals, new indications or labeling for Pluvicto, or regarding potential future revenues from Pluvicto. You should
not place undue reliance on these statements. Such forward-looking statements are based on our current beliefs and expectations regarding
future events, and are subject to significant known and unknown risks and uncertainties. Should one or more of these risks or uncertainties
materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the forward-looking
statements. There can be no guarantee that Pluvicto will be submitted or approved for sale or for any additional indications or labeling
in any market, or at any particular time. Nor can there be any guarantee that Pluvicto will be commercially successful in the future.
In particular, our expectations regarding Pluvicto could be affected by, among other things, the uncertainties inherent in research and
development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government
regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement
pressures and requirements for increased pricing transparency; our ability to obtain or maintain proprietary intellectual property protection;
the particular prescribing preferences of physicians and patients; general political, economic and business conditions, including the
effects of and efforts to mitigate pandemic diseases such as COVID- 19; safety, quality, data integrity or manufacturing issues; potential
or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred
to in Novartis AG’s current Form 20-F on file with the US Securities and Exchange Commission. Novartis is providing the information
in this press release as of this date and does not undertake any obligation to update any forward-looking statements contained in this
press release as a result of new information, future events or otherwise.
About Novartis
Novartis is reimagining medicine to improve and extend people’s lives. We
deliver high-value medicines that alleviate society’s greatest disease burdens through technology leadership in R&D and novel
access approaches. In our quest to find new medicines, we consistently rank among the world’s top companies investing in research
and development. About 108,000 people of more than 140 nationalities work together to bring Novartis products to nearly 800 million people
around the world. Find out more at https://www.novartis.com
Novartis is on Twitter. Sign up to follow @Novartis at https://twitter.com/novartisnews
For Novartis multimedia content, please visit https://www.novartis.com/news/media-library
For questions about the site or required registration, please contact media.relations@novartis.com
References
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1. |
Novartis Data on File. |
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2. |
Nuhn P, De Bono JS, Fizazi K et al. Update on systemic prostate cancer therapies: management of metastatic
castration-resistant prostate cancer in the era of precision oncology. Eur Urol. 2019;75(1):88–99. |
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Sartor O, J. de Bono KN, Chi K, et al. Lutetium-177–PSMA-617 for Metastatic Castration-Resistant Prostate
Cancer. NEJM 2021; doi: 10.1056/NEJMoa2107322. |
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Kirby M, Hirst C, Crawford ED. Characterising the castration-resistant prostate cancer population: a systematic
review. Int J Clin Pract 2011;65(11):1180–92. |
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American Cancer Society. Survival Rates for Prostate Cancer. ACS website. Available online: https://www.cancer.org/cancer/prostate-cancer/detection-diagnosis-staging/survival-rates.html.
Last accessed October 2022. |
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de Bono J et al. Olaparib for Metastatic Castration-Resistant Prostate Cancer. NEJM 2020; doi:10.1056/NEJMoa1911440. |
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de Wit R, de Bono J et al. Cabazitaxel versus Abiraterone or Enzalutamide in Metastatic Prostate Cancer. NEJM 2019; doi: 10.1056/NEJMoa1911206. |
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Komura K et al. Comparison of Radiographic Progression-Free Survival and PSA Response on Sequential Treatment
Using Abiraterone and Enzalutamide for Newly Diagnosed Castration-Resistant Prostate Cancer: A Propensity Score Matched Analysis from
Multicenter Cohort. Journal of clinical medicine 2019; doi:10.3390/jcm8081251. |
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Tannock, I et al. Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer. NEJM 2004; doi:10.1056/NEJMoa040720. |
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Pluvicto [prescribing information]. Millburn, NJ: Advanced Accelerator Applications USA, Inc.; 2022. |
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Advanced Accelerator Applications USA, Inc. PLUVICTO™ Canadian Product Monograph. August 25, 2022. |
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12. |
Pluvicto [Summary of Product Characteristics]. Great Britain. 2022. |
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Novartis Pharmaceuticals. 177Lu-PSMA-617 vs. Androgen Receptor-directed Therapy in
the Treatment of Progressive Metastatic Castrate Resistant Prostate Cancer (PSMAfore). U.S. National Library of Medicine: Clinical Trials.
2020; NCT04689828. |
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Novartis. Press Release. https://www.novartis.com/news/media-releases/novartis-receives-positive-chmp- opinion-pluvicto-patients-progressive-psma-positive-metastatic-castration-resistant-prostate-cancer.
Last accessed October 2022. |
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Novartis Pharmaceuticals. An International Prospective Open-label, Randomized, Phase III Study Comparing
177Lu-PSMA-617 in Combination With Soc, Versus SoC Alone, in Adult Male Patients With mHSPC (PSMAddition). U.S. National Library of Medicine:
Clinical Trials. 2021; NCT04720157. |
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Sung H, Ferlay J, Siegel RL, Sung H, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence
and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209-249. doi:10.3322/caac.21660. |
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Jadvar H. Targeted radionuclide therapy: an evolution toward precision cancer treatment. AJR Am J Roentagenol.
2017;209(2);277-288. |
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Jurcic JG, Wong JYC, Knoc SJ, et al. Targeted radionuclide therapy. In: Tepper JE, Foote RE, Michalski
JM, eds. Gunderson & Tepper’s Clinical Radiation Oncology. 5th ed. Elsevier, Inc. 2021;71(3):209-249. |
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Hope TA, Aggarwal R, Chee B, et al. Impact of 68Ga-PSMA-11 PET on management in patients with biochemically
recurrent prostate cancer. J Nucl Med 2017;58(12):1956–61. |
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Hupe MC, Philippi C, Roth D, et al. Expression of prostate-specific membrane antigen (PSMA) on biopsies
is an independent risk stratifier of prostate cancer patients at time of initial diagnosis. Front Oncol 2018;8:623. |
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Bostwick DG, Pacelli A, Blute M, et al. Prostate specific membrane antigen expression in prostatic intraepithelial
neoplasia and adenocarcinoma: a study of 184 cases. Cancer 1998;82(11):2256–61. |
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Pomykala KL, Czernin J, Grogan TR, et al. Total-body 68Ga-PSMA-11 PET/CT for bone metastasis detection in
prostate cancer patients: potential impact on bone scan guidelines. J Nucl Med 2020;61(3):405–11. |
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Minner S, Wittmer C, Graefen M, et al. High level PSMA expression is associated with early PSA recurrence
in surgically treated prostate cancer. Prostate 2011;71(3):281–8. |
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Hofman MS, Violet J, Hicks RJ et al. [177Lu]-PSMA-617 radionuclide treatment in patients with metastatic castration-resistant
prostate cancer (LuPSMA trial): a single-centre, single-arm, phase 2. |
|
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Sant GR, Knopf KB, Albala DM. Live-single-cell phenotypic cancer biomarkers-future role in precision oncology?
NPJ Precision Oncology 2017;1(1):21. |
# # #
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SIGNATURES
Pursuant to the requirements of the
Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly
authorized.
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Novartis AG |
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Date: December 5, 2022 |
By: |
/s/ PAUL PENEPENT |
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Name: |
Paul Penepent |
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Title: |
Head Group Financial Reporting and Accounting |
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