Company overview | Financial review | 2022 priorities | Appendix | References |
Q2 2022 Results
Investor presentation
1 Investor Relations │ Q2 2022 Results
Company overview | Financial review | 2022 priorities | Appendix | References |
Disclaimer
This presentation contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995, that can generally be identified by words such as "potential," "expected," "will," "planned," "pipeline," "outlook," or similar expressions, or by express or implied discussions regarding potential new products, potential new indications for existing products, potential product launches, or regarding potential future revenues from any such products; or regarding potential future, pending or announced transactions; or regarding potential future sales or earnings of the Group or any of its divisions; or by discussions of strategy, plans, expectations or intentions; or regarding the Group's liquidity or cash flow positions and its ability to meet its ongoing financial obligations and operational needs; or regarding the strategic review of Sandoz; or regarding our commitment to net zero emissions across our value chain by 2040; or regarding our new organizational structure; or our efforts to petition the appeals court to uphold the validity of the Gilenya US dosing regimen patent. Such forward-looking statements are based on the current beliefs and expectations of management 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. You should not place undue reliance on these statements. In particular, our expectations could be affected by, among other things: liquidity or cash flow disruptions affecting our ability to meet our ongoing financial obligations and to support our ongoing business activities; the potential that the strategic benefits, synergies or opportunities expected from our new organizational structure may not be realized or may be more difficult or take longer to realize than expected; the impact of a partial or complete failure of the return to normal global healthcare systems, including prescription dynamics; global trends toward healthcare cost containment, including ongoing government, payer and general public pricing and reimbursement pressures and requirements for increased pricing transparency; uncertainties regarding potential significant breaches of data security or data privacy, or disruptions of our information technology systems; regulatory actions or delays or government regulation generally, including potential regulatory actions or delays with respect to the development of the products described in this presentation; the uncertainties in the research and development of new healthcare products, including clinical trial results and additional analysis of existing clinical data; our ability to obtain or maintain proprietary intellectual property protection, including the ultimate extent of the impact on Novartis of the loss of patent protection and exclusivity on key products; safety, quality, data integrity, or manufacturing issues; uncertainties involved in the development or adoption of potentially transformational technologies and business models; uncertainties regarding actual or potential legal proceedings, investigations or disputes; our performance on environmental, social and governance measures; general political, economic and business conditions, including the effects of and efforts to mitigate pandemic diseases such as COVID-19; uncertainties regarding future global exchange rates; uncertainties regarding future demand for our products; 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 presentation as of this date and does not undertake any obligation to update any forward-looking statements as a result of new information, future events or otherwise.
2 Investor Relations │ Q2 2022 Results
Company overview | Financial review | 2022 priorities | Appendix | References |
Vas Narasimhan
Chief Executive Officer
Company overview
3 Investor Relations │ Q2 2022 Results
Company overview | Financial review | 2022 priorities | Appendix | References |
Novartis delivers solid Q2 performance across our value drivers
Growth, cc | 1 | Innovation | 3 | |
Group sales Q2 +5% (H1 +5%) | Cosentyx® childhood arthritic conditions approved in EU | |||
IM sales Q2 +5% (H1 +5%) | Kymriah® r/r FL approved in US and EU | |||
Sandoz sales Q2 +5% (H1 +6%) | Scemblix® Ph+ CML received positive CHMP opinion | |||
Productivity, cc | 2 | ESG | 4 | ||
Group core operating income Q2 +5% (H1 +7%) | Innovation NTDs: USD 250m R&D investment over 5 years | ||||
IM core operating income Q2 +6% (H1 +6%) | (Kigali declaration) | ||||
Innovation CT diversity: >USD 50m commitment over 10 years | |||||
IM core margin Q2 37.2%, +0.5%pts (H1 36.6%) | |||||
(Beacon of Hope) | |||||
Sandoz core operating income Q2 -4%(H1 +10%) | |||||
MSCI upgrades Novartis to AA: Now top quartile within the industry | |||||
SG&A savings expected to increase to ~USD 1.5bn by 2024 | |||||
Constant currencies (cc), core results are non-IFRS measures; explanation can be found on page 47 of Condensed Interim Financial Report. Unless otherwise noted, all growth rates refer to same period in PY. IM - Innovative Medicines division r/r FL - relapsed or refractory follicular lymphoma GvHD - acute and chronic graft-versus-host disease CML - chronic myeloid leukemia NTDs - Neglected tropical diseases CT - Clinical trial
4 Investor Relations │ Q2 2022 Results
Company overview | Financial review | 2022 priorities | Appendix | References |
1 GROWTH
Q2 Innovative Medicines (IM) sales grew across US and ex-US, driven by our in-market growth drivers
IM sales USD 10.5bn (+5% cc) | Growth drivers +21% cc, 59% of IM sales | |||||||||||
US | Q2 2022 USD 3.9bn | Ex-US | Q2 2022 USD 6.5bn | Q2 2022 USD 6.1bn | ||||||||||
+5% cc | 59% | Cosentyx | ||||||||||
Zolgensma | ||||||||||||
+6% cc | 51% | +21% vs. PY | Kisqali | |||||||||
Scemblix | ||||||||||||
Other1 | ||||||||||||
Q2 2021 | Q2 2022 | Q2 2021 | Q2 2022 | Q2 2021 | Q2 2022 |
All % growth relate to cc unless otherwise stated 1. Includes Promacta®, Taf-Mek®, Jakavi®, Ilaris®, Kymriah®, Xiidra®, Lutathera®, Piqray®, Mayzent®, Aimovig®, Xolair®, Beovu®, Adakveo®, Tabrecta®, Enerzair®, Atectura® , Luxturna®, Pluvicto™
5 Investor Relations │ Q2 2022 Results
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Novartis AG published this content on 19 July 2022 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 19 July 2022 05:23:03 UTC.