CSL Limited Tender Offer to Acquire 100% of Vifor Pharma Ltd 14 December, 2021

Paul Perreault Joy Linton CEO and MD CFO

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES.

This investor presentation ( Presentation ) is dated 14 December 2021 and has been prepared and authorised by CSL Limited (ABN 99 051 588 348) ( CSL ). By accepting this Presentation, you represent and warrant that you are entitled to receive this Presentation in accordance with the restrictions and agree to be bound by the limitations contained within it. This Presentation includes information about:

CSL's proposed acquisition of Vifor Pharma Ltd. ( Vifor Pharma ); and
CSL's proposed capital raising to partly fund the proposed acquisition of Vifor Pharma ( Proposed Acquisition ), comprising a fully underwritten institutional placement ( Placement ) of new fully paid ordinary shares in CSL ( New Shares ) and a non-underwritten offer of New Shares to eligible shareholders under a share purchase plan ( SPP , and together with the Placement, the Offer ).

Important Notices and Disclaimer

SUMMARY INFORMATION

This Presentation contains summary information about CSL and its controlled entities (the Group ) and the Group's activities which is current only as at the date of this Presentation (unless otherwise stated). The information in this Presentation is of a general nature and does not purport to be complete. This Presentation does not purport to contain all of the information that an investor should consider when making an investment decision nor does it contain all of the information that would be required to be included in a prospectus or product disclosure statement prepared in accordance with the requirements of the Corporations Act 2001 (Cth) (the Corporations Act ). CSL's historical information in this Presentation is, or is based upon, information that has been released to the Australian Securities Exchange ( ASX ). This Presentation should be read in conjunction with CSL's other periodic and continuous disclosure announcements lodged with the ASX, which are available at www.asx.com.au.

Certain information in this Presentation (including financial information – whether audited, unaudited, historical or anticipated) has been sourced from Vifor Pharma and its associates. While steps have been taken to review that information, no representation or warranty, expressed or implied, is made as to its fairness, accuracy, correctness, completeness or adequacy. For more information, see “Reliance on information provided” in Appendix B: Key Risks in this Presentation. Certain market and industry data used in connection with this Presentation may have been obtained from research, surveys or studies conducted by third parties, including industry or general publications. Neither CSL nor its representatives have independently verified any such market or industry data provided by third parties or industry or general publications.

ROUNDING

A number of figures, amounts, percentages, estimates, calculations of value and fractions in this Presentation are subject to the effect of rounding. Accordingly, the actual calculation of these figures may differ from the figures set out in this Presentation.

NOT FINANCIAL PRODUCT ADVICE

This Presentation is for information purposes only and is not a prospectus, disclosure document, product disclosure statement or other offering document under Australian law (and will not be lodged with the Australian Securities and Investments Commission ( ASIC )) or the law of any other jurisdiction. This Presentation is not financial product advice or investment advice nor a recommendation to acquire New Shares and has been prepared without taking into account the objectives, financial situation and particular needs of particular investors. Before making an investment decision, prospective investors should consider the appropriateness of the information having regard to their own objectives, financial situation and needs, and seek appropriate advice, including financial, legal and taxation advice, appropriate to their jurisdiction. CSL is not licensed to provide financial product advice in respect of the New Shares.

FINANCIAL INFORMATION

All dollar values contained in this document are expressed in United States dollars unless otherwise stated or the context requires otherwise.

CSL prepares its financial information in accordance with the Corporations Act, Australian Accounting Standards ( AAS ), and other authoritative pronouncements of the Australian Accounting Standards Board ( AASB ) and International Financial Reporting Standards ( IFRS ) adopted by the International Accounting Standards Board ( IASB ).

This Presentation includes certain pro forma financial information to reflect the impact of the Proposed Acquisition and the Offer. The pro forma historical financial information provided in this Presentation is for illustrative purposes only and is not represented as being indicative of CSL’s views on its future financial position and/or performance or any scale benefits, synergies or opportunities that may be realised as a result of the Proposed Acquisition. The pro forma historical financial information has been prepared by CSL in accordance with the measurement and recognition requirements, but not disclosure requirements, prescribed by the AAS, and has not been subject to audit or review. The purchase price accounting for the Proposed Acquisition in this Presentation has been shown on an illustrative basis. CSL will undertake a formal fair value assessment of all of the tangible and intangible assets, liabilities and contingent liabilities of Vifor Pharma post-acquisition, which may give rise to different values to those used for the purposes of the pro forma financial information set out in this Presentation. The pro forma financial information included in this Presentation does not purport to be in compliance with Article 11 of Regulation S-X of the rules and regulations of the U.S. Securities and Exchange Commissionor Article 3-05 of Regulation S-X .

Investors should be aware that certain financial measures included in this Presentation are “non-IFRS financial information” under ASIC Regulatory Guide 230: “Disclosing non-IFRS financial information” published by ASIC and also “nonGAAP financial measures” within the meaning of Regulation G under the U.S. Securities Exchange Act of 1934 and are not recognised under the AAS or IFRS. The non-IFRS financial information and non-GAAP financial measures in this Presentation include EBITDA, EBIT, EBIT margin, net debt, free cash flow, gearing, leverage and net leverage. CSL believes the non-IFRS financial information and non-GAAP financial measures provide useful information to investors in measuring the financial performance and condition of its business. However, investors should note that the non-IFRS financial information and non-GAAP financial measures do not have standardised meanings prescribed by the AAS or IFRS. Therefore, the non-IFRS financial information is not a measure of financial performance, liquidity or value under the IFRS and may not be comparable to similarly titled measures presented by other entities, nor should the information be construed as an alternative to other financial measures determined in accordance with the AAS or IFRS. Investors are cautioned not to place undue reliance on any non-IFRS financial information or non-GAAP financial measures included in this Presentation.

FORWARD LOOKING STATEMENTS

This Presentation contains statements that constitute forward-looking statements. The forward-looking statements contained in this Presentation include statements regarding CSL’s intent, belief or current expectations with respect to the timetable, conduct and outcome of the Offer and the use of Offer proceeds, statements about the Proposed Acquisition, statements about the plans, objectives and strategies of the management of CSL, statements about the industry and markets in which the Group operates, and statements about the future performance of the Group's business and its financial condition, future earnings, distributions and performance, indicative drivers and forecasted economic indicators. The words “anticipate”, “believe”, “expect”, "estimate", "aim", “project”, “forecast”, “estimate”, "risk", “likely”, “intend”, “outlook”, “should”, “could”, "would", “may”, "will", "continue", "plan", "probability", "indicative", "seek", “target”, “plan” and other similar expressions are intended to identify forward-looking statements.

You are strongly cautioned not to place undue reliance on forward-looking statements, including in respect of CSL's future financial performance and outlook, particularly in light of the current economic climate and the significant volatility, uncertainty and disruption caused by COVID-19.

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NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

Any such statements, opinions and estimates in this Presentation speak only as of the date hereof and are based on assumptions and contingencies subject to change without notice, as are statements about market and industry trends, projections, guidance and estimates. Forward-looking statements are provided as a general guide only. The forward-looking statements in this Presentation are not indications, guarantees or predictions of future performance and involve known and unknown risks (including (without limitation) the risks and uncertainties associated with CSL, the Group, the business of the Group, the Proposed Acquisition and the other risks set out in Appendix B: Key Risks to this Presentation), uncertainties and other factors, many of which are beyond the control of CSL, its officers, employees, agents and advisors, and may involve significant elements of subjective judgement and assumptions as to future events which may or may not be correct, and may cause actual results to differ materially from those expressed or implied in such statements. Forward-looking statements may also assume the success of CSL's business strategies. The success of any of these strategies is subject to uncertainties and contingencies beyond CSL's control, and no assurance can be given that any of the strategies will be effective or that the anticipated benefits from the strategies will be realised in the period for which the forward looking statements may have been prepared or otherwise.

Important Notices and Disclaimer (Cont’d)

There can be no assurance that actual outcomes will not differ materially from these statements. There are usually differences between forecast and actual results because events and actual circumstances frequently do not occur as forecast and their differences may be material. A number of important factors could cause actual results or performance to differ materially from the forward-looking statements, including (without limitation) the risks and uncertainties associated with the ongoing impacts of COVID-19, the Australian, US, European and global economic environment and capital market conditions and other risk factors set out in this Presentation. Investors should consider the forward-looking statements contained in this Presentation in light of those risks and disclosures. The forward-looking statements are based on information available to CSL as at the date of this Presentation. None of CSL, the underwriters for the Placement and lead managers for the Offer ( Joint Lead Managers ), or any other person, gives any representation, warranty or assurance, or guarantees that the occurrence of the events expressed or implied in any forward-looking statement will occur.

Each recipient of this Presentation should make its own enquiries and investigations regarding all information included in this Presentation, including the assumptions, uncertainties and contingencies that may affect CSL's future operations and the values and the impact that future outcomes may have on CSL.

To the maximum extent permitted by law, CSL, the Joint Lead Managers and each of their respective advisors, affiliates, related bodies corporate, directors, officers, partners, employees and agents ( Extended Parties ) disclaim any responsibility for the accuracy or completeness of any forward-looking statements whether as a result of new information, future events or results or otherwise. To the maximum extent permitted by law, each of CSL and the Joint Lead Managers and their respective Extended Parties disclaim any responsibility to update or revise any forward-looking statement to reflect any change in CSL's financial condition, status or affairs or any change in the events, conditions or circumstances on which a statement is based, except as required by Australian law.

PAST PERFORMANCE

Past performance and pro forma historical financial information in this Presentation is provided for illustrative purposes only and should not be relied upon and is not an indication of future performance, including future share price information. Historical information in this Presentation relating to CSL is information that has previously been released to the market. For further details on that historical information, please see past announcements released to the ASX.

INVESTMENT RISKS

An investment in CSL is subject to investment risks including possible loss of income and principal invested. CSL does not guarantee any particular rate of return or the performance of CSL. Recipients should read the risks set out in Appendix B: Key Risks to this Presentation for a non-exhaustive summary of the key risks that may affect CSL and its financial and operating performance.

NOT AN OFFER

This Presentation is not and should not be considered an offer or an invitation to acquire New Shares or any other financial products in any jurisdiction and does not and will not form any part of any contract for the acquisition of New Shares.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

This Presentation may not be distributed or released in the United States. This Presentation does not constitute an offer to sell, or the solicitation of an offer to buy, any securities in the United States, or in any other jurisdiction in which such an offer would be unlawful. The New Shares to be offered and sold under the Offer have not been, and will not be, registered under the U.S. Securities Act of 1933 (the U.S. Securities Act ) or the securities laws of any state or other jurisdiction of the United States. Accordingly, the New Shares may not be offered or sold to any person in the United States, except pursuant to an exemption from, or in a transaction not subject to, the registration requirements of the U.S. Securities Act and any other applicable securities laws of any state or other jurisdiction of the United States.

By accepting this Presentation you represent and warrant that you are entitled to receive such Presentation in accordance with the above restrictions and agree to be bound by the limitations contained herein. The distribution of this Presentation (including an electronic copy) may be restricted by law in certain other countries. You should read the important information set out in Appendix D: International Offer Restrictions to this Presentation. Failure to comply with these restrictions may constitute a violation of applicable securities laws.

THE JOINT LEAD MANAGERS

Each Joint Lead Manager, together with its respective affiliates, is a full service securities firm and commercial bank engaged in various activities, which may include in securities, commodities and derivatives trading, foreign exchange and other brokerage activities, and principal investing, as well as providing investment, corporate and private banking, asset and investment management, financing and financial advisory services and other commercial services and products to a wide range of corporations, governments and individuals for which they have received or may receive customary fees and expenses or other transaction consideration. In the course of these activities, the Joint Lead Managers and their respective affiliates may at any time for their own account and for the accounts of their clients make or hold investments in equity securities or other financial products of CSL or its affiliates, and receive customary fees and expenses or other transaction consideration in respect of such activities. In the course of these activities, the Joint Lead Managers and their respective affiliates may at any time for their own account and for the accounts of their clients make or hold investments in equity securities or other financial products of CSL or its affiliates, and receive customary fees and expenses or other transaction consideration in respect of such activities. The Joint Lead Managers are acting as joint lead managers and underwriters to the Placement for which they have received or expect to receive fees and reimbursement of expenses. One or more Joint Lead Managers or their respective affiliates may be or may become lenders to CSL or its related bodies corporate under certain loan facilities, and affiliates of one or more Joint Lead Managers may have or enter into derivative exposures involving CSL or its related bodies corporates, including exposures to hedge the interest rate or currency risk associated with the financing or making of the Proposed Acquisition. The Joint Lead Managers and their respective affiliates may receive fees, make profits or avoid losses and be reimbursed for expenses in connection with these activities. The Joint Lead Managers (and/or their respective affiliates) are underwriting the Placement only. The Joint Lead Managers are acting for and providing services to CSL in relation to the Offer and will not be acting for or providing services to CSL shareholders or creditors. Each of the Joint Lead Managers has been engaged solely as an independent contractor and is acting solely in a contractual relationship on an arm’s length basis with CSL. The engagement of the Joint Lead Managers by CSL is not intended to create any agency or other relationship between the Joint Lead Managers and CSL shareholders or creditors.

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NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

In connection with the Placement, one or more institutional investors may elect to acquire an economic interest in the New Shares ( Economic Interest ), instead of subscribing for or acquiring the legal or beneficial interest in those securities. A Joint Lead Manager (or its affiliates) may, for its own account, write derivative transactions with those investors relating to the New Shares to provide the Economic Interest, or otherwise acquire New Shares in connection with the writing of those derivative transactions in the Placement and/or the secondary market. As a result of those transactions, a Joint Lead Manager (and/or its affiliates) may be allocated, subscribe for or acquire New Shares or shares of CSL in the Placement and/or the secondary market, including to hedge those derivative transactions, as well as hold long or short positions in those securities. These transactions may, together with other shares in CSL acquired by a Joint Lead Manager or its affiliates in connection with their ordinary course sales and trading, principal investing and other activities, result in that Joint Lead Manager or its affiliates disclosing a substantial holding and earning fees. A summary of the key terms of the underwriting agreement between CSL and the Joint Lead Managers is provided in Appendix C.

DISCLAIMER

Important Notices and Disclaimer (Cont’d)

While the information in this Presentation has been prepared in good faith and with reasonable care, no representation or warranty, express or implied, is made as to the accuracy, adequacy or reliability of any statements, estimate, opinions or other information contained in the Presentation. The information in this Presentation is subject to change without notice.

None of the Joint Lead Managers, or any of their or CSL’s respective Extended Parties, have authorised, permitted or caused the issue, lodgement, submission, dispatch or provision of this Presentation and none of them makes or purports to make any statement in this Presentation and there is no statement in this Presentation which is based on any statement by any of them.

To the maximum extent permitted by law, CSL, the Joint Lead Managers and their respective Extended Parties:

expressly exclude and disclaim all liabilities (including, without limitation, liability for negligence) in respect of any direct or indirect expenses, losses, damages or costs incurred as a result of participation in the Offer, or failure to participate in, or the information in this Presentation being inaccurate or incomplete in any way for any reason, whether by negligence or otherwise; and
make no representation or warranty, express or implied, as to the fairness, currency, accuracy, reliability or completeness of information, opinions and conclusions in this Presentation and take no responsibility for any part of this Presentation. No person is authorised to give any information or make any representation in connection with the Offer that is not contained in this Presentation. Any information or representation not contained in this Presentation may not be relied on as having been authorised by CSL in connection with the Offer. The Joint Lead Managers and their respective Extended Parties take no responsibility for any information in this Presentation, for any action taken by you on the basis of such information or for the Offer and make no recommendations as to whether any person should participate in the Offer nor do they make any representations or warranties concerning the Offer or any such information, and they disclaim any fiduciary relationship between them and the recipients of this Presentation, or any duty to the recipients of this Presentation or participants in the Offer.

You represent, warrant and agree that you have not relied on any statements made by a Joint Lead Manager or any of its Extended Parties in relation to the New Shares or the Offer generally and you further expressly disclaim that you are in a fiduciary relationship with any of them. To the maximum extent permitted by law, you agree to release and indemnify the Joint Lead Managers and their respective Extended Parties from and against all claims, losses, liabilities, expenses, costs, actions, damages, remedies or other matters, whether in tort, contract or under law or otherwise, arising from or which may arise from or in connection with the provision of, or any purported reliance on, this Presentation and you covenant that no claim or allegations will be made against the Joint Lead Managers or their respective Extended Parties in relation to this Presentation.

This Presentation is not an offer or invitation for subscription or purchase of or a recommendation of securities. It does not take into account the investment objectives, financial situation and particular needs of the investor. Before making an investment in CSL, the investor or prospective investor should consider whether such an investment is appropriate to their particular investment needs, objectives and financial circumstances and consult an investment adviser if necessary.

Information, including forecast financial information, in this presentation should not be considered as a recommendation in relation to holding, purchasing or selling shares, securities or other instruments in CSL or any other entity. Due care and attention has been used in the preparation of forecast information. However, actual results may vary from forecasts and any variation may be materially positive or negative. Forecasts by their very nature are subject to uncertainty and contingencies, many of which are outside the control of CSL. Past performance is not a reliable indication of future performance.

You acknowledge and agree that determination of eligibility of investments for the purposes of the Placement and SPP is determined by reference to a number of matters, including legal requirements and the discretion of CSL and the Joint Lead Managers and each of CSL, the Joint Lead Managers and their respective Extended Parties disclaim any duty or liability (including for negligence) in respect of the exercise or otherwise of that discretion, to the maximum extent permitted by law.

You acknowledge and agree that your existing holding will be estimated by reference to CSL's beneficial register on 13 December 2021 which shows historical holdings as at that date and is not up to date. There will be no verification or reconciliation of the holdings as shown in the historical beneficial register and accordingly this may not truly reflect your actual holding. CSL and the Joint Lead Managers do not have any obligation to reconcile assumed holdings (eg, for recent trading or swap positions) when determining allocations nor do they have any obligation to allocate pro rata on the basis of existing shareholdings. If you do not reside in a permitted offer jurisdiction you will not be able to participate in the Placement. Each of CSL, the Joint Lead Managers and their respective Extended Parties disclaim any duty or liability (including for negligence) in respect of the determination of your allocation using your assumed holdings.

You further acknowledge and agree that allocations are at the sole discretion of CSL and/or the Joint Lead Managers. Each of CSL, the Joint Lead Managers and their respective Extended Parties disclaim any duty or liability (including for negligence) in respect of the exercise or otherwise of that discretion, to the maximum extent permitted by law. Furthermore, CSL and the Joint Lead Managers reserve the right to change the timetable in their absolute discretion including by closing the Placement bookbuild early or extending the Placement bookbuild closing time (generally or for particular investor(s)) in their absolute discretion (but have no obligation to do so), without recourse to them or notice to you. Furthermore, communications that a transaction is “covered” (i.e. aggregate demand indications exceed the amount of the shares offered) are not an assurance that the transaction will be fully distributed.

WITHDRAWAL AND COOLING-OFF

CSL reserves the right to withdraw or vary the timetable for the Offer without notice. Cooling off rights do not apply to an investment in New Shares.

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Transaction Highlights

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Expands CSL’s leadership across an attractive portfolio focused on Renal Disease and Iron Deficiency

Complements CSL’s existing therapeutic focus areas and high quality pipeline

CSL’s global reach, R&D capabilities and resources augment the delivery of Vifor Pharma’s products to patients

Expected to be low-to-mid teens NPATA per share accretive in the first full year of CSL ownership[1] , including full run rate cost synergies[2]

Acquisition consideration[3] of US$12.3 billion / A$17.2 billion funded via US$4.5 billion / A$6.3 billion underwritten Placement[4] , US$6.0 billion / A$8.4 billion new debt and existing cash / undrawn facilities

CSL confirms FY22 NPAT guidance of c. US$2,150 million – US$2,250 million @ CC[5]

Note: USD converted to AUD at spot FX of 1.406 and CHF converted to USD at spot FX of 1.083 as at 13 December 2021.

1. NPATA per share reflects net profit after tax excluding amortisation (post-tax) and excludes one-off transaction costs and integration costs. The Transaction is also expected to be immediately EPS accretive in the first full year of CSL ownership (expected to be FY23) on an EPS reported basis including the amortisation of intangibles recognised as a result of the acquisition based on a preliminary estimate of purchase price accounting.

2. Full run rate annual pre-tax cost synergies of US$75 million expected to phase in over three years post acquisition close.

3. Total acquisition consideration based on offer price of US$179.25 per share, fully diluted shares on issue of 65 million, and debt of CHF 540 million. Excludes transaction costs.

4. CSL will also undertake a non-underwritten Share Purchase Plan (“SPP”) to eligible CSL shareholders. The SPP is targeting to raise up to A$750 million.

5. Constant Currency (CC) removes the impact of exchange rate movements to facilitate comparability. Refer to the analyst presentation regarding CSL's annual financial results for the financial year ended 30 June 2021 lodged with the ASX on 18 August 2021 for further information regarding constant currency calculations.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

Transaction Summary

Tender Offer to acquire 100% of Vifor Pharma

Transaction Overview

CSL and Vifor Pharma today announced that they have entered into a definitive agreement under which CSL has agreed to launch an all-cash public Tender Offer ( Tender Offer ) to acquire all publicly held Vifor Pharma shares for US$179.25 per Vifor Pharma share, payable in U.S. dollars (the Transaction )
The Tender Offer represents an aggregate equity value for Vifor Pharma of US$11.7 billion / A$16.4 billion
Tender Offer is unanimously recommended for acceptance by Vifor Pharma’s Board of Directors
Patinex AG, Vifor Pharma's largest shareholder holding 23.2% of Vifor’s share capital, has agreed to tender its shares
The Transaction is to be funded via:
A fully underwritten institutional placement ( Placement ) of A$6.3 billion (US$4.5 billion)

Transaction Funding

A fully committed debt bridge facility of US$6.0 billion / A$8.4 billion, to be replaced with longer term debt financing, including capital markets
Existing cash / undrawn facilities of US$2.0 billion / A$2.8 billion[1]
CSL will also undertake a non-underwritten Share Purchase Plan ( SPP ) to eligible CSL shareholders[2 ] in Australia and New Zealand. The SPP is targeting to raise up to A$750 million (US$534 million)

Financial Impact

Expected to be low-to-mid teens NPATA per share accretive in the first full year of CSL ownership[3] , including full run rate cost synergies[4]
CSL’s balance sheet strength will be retained with pro forma FY21 net debt / EBITDA of approximately 2.65x and a clear de-leveraging profile

• The Tender Offer is currently expected to commence around 18 January 2022, by means of the publication of the Tender Offer prospectus and is expected to complete around the middle of calendar year 2022

Timing and Tender Conditions

Main terms and conditions of the Tender Offer have been published in today’s Pre-Announcement of the Tender Offer, and full details including terms and conditions will be published in the Tender Offer prospectus
The Tender Offer remains subject to the conditions as set out in the Pre-Announcement of the Tender Offer published today including:
CSL having received, by the end of the main offer period of the Tender Offer, acceptances for such number of Vifor Pharma shares representing at least 80% of the fully diluted share capital of Vifor Pharma as at the end of the main offer period of the Tender Offer (as more fully described in the Pre-Announcement); and Further customary offer conditions, including regarding the receipt of regulatory approvals
- Note: USD converted to AUD at spot FX of 1.406 and CHF converted to USD at spot FX of 1.083 as at 13 December 2021. 1. Inclusive of estimated transaction costs of US$200 million.
2. Eligible Shareholders are shareholders with a registered address in Australia or New Zealand and who are outside the United States on the register as at 7:00pm (AEDT) on Monday, 13 December 2021. 3. NPATA per share reflects net profit after tax excluding amortisation (post-tax) and excludes one-off transaction costs and integration costs. The Transaction is also expected to be immediately EPS accretive in the first full year of CSL ownership (expected to be FY23) on an EPS reported basis including the amortisation of intangibles recognised as a result of the acquisition based on a preliminary estimate of purchase price accounting.

4. Full run rate annual pre-tax cost synergies of US$75 million expected to phase in over three years post acquisition close.

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Compelling Strategic Rationale

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1
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Strengthens CSL’s Value Driven Strategy

Vifor Pharma adds a durable and growing business with leadership positions across complementary and adjacent franchises, delivering greater benefit to patients.

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2
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Builds a Significant Renal Franchise

Partner of choice in growing renal disease market with over US$25 billion[1] opportunity. CSL’s global reach, R&D capabilities and financial scale will enable global expansion.

Extends the Reach of CSL’s High Value Pipeline

Enhanced access to unique patient population supports clinical trial execution. Complementary portfolio.

Materially Enhances Scale and Free Cash Flow

Revenue increase of 19% on pro forma FY21 and robust pro forma FY21 free cash flow[2] .

US$75 million of run rate pre-tax cost synergies expected, phased in over three years post acquisition close.

Compelling Financial Profile

Expected to be low-to-mid teens NPATA per share accretive in the first full year of CSL ownership[3] , including full run rate cost synergies[4] , while retaining balance sheet flexibility.

1. Estimated relevant market in 2026. Evaluate Pharma & Vifor Pharma analysis, excluding metabolic syndrome. 2. Free cash flow calculated as cash flow from operating activities less net capex.

3. NPATA per share reflects net profit after tax excluding amortisation (post-tax) and excludes one-off transaction costs of and integration costs. The Transaction is also expected to be immediately EPS accretive in the first full year of CSL ownership (expected to be FY23) on an EPS reported basis including the amortisation of intangibles recognised as a result of the acquisition based on a preliminary estimate of purchase price accounting.

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4. Full run rate annual pre-tax cost synergies of US$75 million expected to phase in over three years post acquisition close.

Vifor Pharma Overview

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Overview of Vifor Pharma

Net Sales Breakdown by Products

CHF Millions, %

 Leader in attractive therapeutic areas across

Nephrology, Dialysis and Iron Deficiency with a focus on product innovation

 Scalable global pharmaceutical platform with

CHF 1,793 million revenue, CHF 576 million EBITDA[1 ] and strong cash generation
Unique partnership with Fresenius Medical Care , the global leader in dialysis

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Other
Ferinject
19%
36%
Veltassa
7%
LTM Jun-21
CHF 1,719m [1]
Velphoro
11%
ESA
28%
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Net Sales Breakdown by Markets

 Proven partner of choice in nephrology

Attractive growth , with up to four product launches expected in 2022 / 23 and growing pipeline
~2,600 employees worldwide, across 22 countries

CHF Millions, %

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Rest of World
12%
Rest of
LTM Jun-21 United
Europe
26% CHF 1,719m [1] States
55%
Switzerland
7%
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Represents LTM Jun-21. US$1,971 million revenue, US$1,889 million net sales and US$634 million EBITDA, representing CHF converted to USD at average of daily FX for LTM period ending Jun-21 of 1.099. Revenue includes Net Sales and Other Income of CHF75m (US$82m).

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Attractive Product Portfolio

Nephrology Dialysis Iron Launching the next generation of therapies Driving value through joint company Accelerated post COVID growth through HF, addressing kidney disease progression with Fresenius and beyond PBM and geographic expansion 2 1 In Market 3 4 5 Vadadustat[6] Heart failure opportunity Pipeline & geographic expansion Sparsentan[7] Vamifeport INS-3001 SNF-472 Source of Durability and Growth Leading Iron Replacement Franchise Expected Near Term Launch Note: HF = heart failure. PBM = patient blood management. 1. Licensed from F. Hoffman-La Roche AG. 5. Licensed from Cara Therapeutics, Inc. 2. Licensed from Pfizer Inc. 6. Licensed from Akebia Therapeutics, Inc., subject to certain conditions and 3. Licensed from ChemoCentryx, Inc. limited to selling Vadadustat to certain providers within the US dialysis market. NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES 4. Licensed from OPKO Health, Inc. 7. Licensed from Travere Therapeutics, Inc.

Global Leadership in Nephrology Empowered by Unique Partnership with Fresenius Medical Care

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STRONG IRON AND PHARMA EXPERTISE GLOBAL LEADERSHIP IN NEPHROLOGY
• Clinical development 55% THROUGH:
Stake
• Manufacturing, regulatory and market access
Close collaboration Better sourcing
experiences on global scale of innovation
GLOBAL LEADER IN DIALYSIS
Access to patient Improving outcomes
~350,000 >54 million >4,000 data and faster via treatment
Kidney disease dialysis treatments p.a. [1] clinics [1] clinical trial execution algorithms
patients [1]
45%
Stake
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1. Figures as at 2020 per Fresenius Medical Care Factsheet 2020.

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Excellent Track Record Across New Product Sourcing, Development and Launch

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Launch 2016
2 Vadadustat [7]
Revenue
5 6
Sparsentan [9]
Launch 2015
Creation of
VFMCRP Up to four product launches expected in 2022 / 23:
Korsuva™ [6] , Tavneos™ [2] , Rayaldee [® 5] and Vadadustat [7]
in 2010
Launch 2018 SNF-472 INS-3001
Initial Portfolio Portfolio Expansion
1 1 3 6
Potential BD&L
Portfolio Vadadustat [7] Sparsentan [9]
4 opportunities
2 5
2010 2015 2020 2025+
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Note: VFMCRP = Vifor Fresenius Medical Care Renal Pharma. 6. Licensed from Cara Therapeutics, Inc. 1. Sales in chronic kidney disease (CKD). 7. Licensed from Akebia Therapeutics, Inc., subject to certain 2. Licensed from ChemoCentryx, Inc. conditions and limited to selling Vadadustat to certain providers 3. Licensed from F. Hoffmann-La Roche AG. within the US dialysis market. 4. Licensed from Pfizer Inc. 8. Licensed from Travere

8. Licensed from Travere Therapeutics, Inc.

5. Licensed from OPKO Health, Inc.

Strong Portfolio of Pre-Commercial Products with Up to Four Launches Expected in 2022 / 23

	Indication	Differentiation	Geography	Status
1	• Moderate to severeCKD-associated pruritis (CKD-aP)in patients receiving haemodialysis • Affects ~70% of all patients on dialysis	• Only approved therapy for CKD- aPandfirst-in-class peripherally acting KORAwithbest-in-class selectivity	Global ex. Japan and South Korea	FQ3 2022: Planned US promotional launch FQ4 2022: EMA approval expected
2	• ANCA associated vasculitis (AAV), a rare, systemic severe small vessel vasculitis with potential for organ damage and acute mortality risk	• Novel targeted treatmentfor AAV that achieves effective and sustained vasculitis control	Ex-US	FQ4 2022: Potential Europe launch
3	• Secondary hyperparathyroidism (SHPT)in adults with CKD • SHPT manifests early and is acritical component of CKD-mineral and bone disorder	• First and only extended release prohormoneof the active form of Vitamin D for SHPT • Convenient once daily oral regimen	Europe and select ex-US territories4	FQ3 2022: Planned Europe launch
Vadadustat5	• Treatment ofanaemia related to CKD	• Potential first-to-market HIF-PH • Improved compliancedue to oral application vs. IV	US (select haemodialysis centers, excluding DaVita)5	March 2022: Potential FDA approval

1. Licensed from Cara Therapeutics, Inc. 2. Licensed from ChemoCentryx, Inc.

3. Licensed from OPKO Health, Inc.

4. Represents Europe, UK, China, Canada, Turkey, New Zealand, and Australia.

5. Licensed from Akebia Therapeutics, Inc., subject to certain conditions and limited to selling Vadadustat to certain providers within the US dialysis market.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

Novel Pipeline of Primarily Mid-to-Late Stage Assets

	Indication	Mechanism of Action	Key Milestones
Sparsentan1	• Focal segmental glomerulosclerosis (FSGS)and IgA nephropathy (IGAN) • Potential toprogress to end-stage kidney disease	• First-in-class, orally active dual antagonistof endothelin and angiotensin II receptors associated with kidney disease progression	• FY22:Potentialsubmissionof combined IgANandFSGS MAA in Europe
SNF-472	• Calcific uremic arteriolopathy(CUA, Calciphylaxis ) andperipheral artery disease(PAD) in patients withend-stage kidney disease on dialysis • Currentlyno approved medicines	• Blocks the formation and growth of hydroxyapatite crystalsin blood vessels	• Feb-21:Grantedorphan drug designation by FDA forPAD
Vamifeport	• Rare diseases characterised by ineffective erythropoiesis and iron overload including beta-thalassemiaandsickle cell disease (SCD)	• Oral ferroportin inhibitor toinhibit both dietary iron absorption and excessive iron releaseinto the blood	• Jan-21: Granted orphan drug designation by FDAfor SCD • Jun-19:Grantedorphan drug designation by FDA and EMA forbeta-thalassemia
INS-3001	• Peripheral artery disease and Aortic valve stenosisinnon-dialysis chronic kidney disease	• Subcutaneously administered; Blocks the formation and growth of hydroxyapatite crystalsin blood vessels	• 4Q 2021: Launching Phase I trial

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1. Licensed from Travere Therapeutics, Inc.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

History of Driving Growth and Value Through Strategic Partnerships

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Strategic Commercial
1 2 JV in Nephrology 3 Product Partnerships
Partnerships
Enhancing Commercial Presence Leadership in Nephrology Expanding the Product Portfolio
Local Partners Joint Company Focus on In-Licensing
• • •
Shared investment Shared investment Regional and global deals
• • •
Complementary strengths Complementary strengths Pure commercial and R&D
•
Collaboration across several areas
Joint Company with
Fresenius Kabi in China
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Strategic Rationale

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Compelling Strategic Rationale

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1
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Strengthens CSL’s Value Driven Strategy

Vifor Pharma adds a durable and growing business with leadership positions across complementary and adjacent franchises, delivering greater benefit to patients.

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2
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Builds a Significant Renal Franchise

Partner of choice in growing renal disease market with over US$25 billion[1] opportunity. CSL’s global reach, R&D capabilities and financial scale will enable global expansion.

Extends the Reach of CSL’s High Value Pipeline

Enhanced access to unique patient population supports clinical trial execution. Complementary portfolio.

Materially Enhances Scale and Free Cash Flow

Revenue increase of 19% on pro forma FY21 and robust pro forma FY21 free cash flow[2] .

US$75 million of run rate pre-tax cost synergies expected, phased in over three years post acquisition close.

Compelling Financial Profile

Expected to be low-to-mid teens NPATA per share accretive in the first full year of CSL ownership[3] , including full run rate cost synergies[4] , while retaining balance sheet flexibility.

1. Estimated relevant market in 2026. Evaluate Pharma & Vifor Pharma analysis, excluding metabolic syndrome. 2. Free cash flow calculated as cash flow from operating activities less net capex.

3. NPATA per share reflects net profit after tax excluding amortisation (post-tax) and excludes one-off transaction costs and integration costs. The Transaction is also expected to be immediately EPS accretive in the first full year of CSL ownership (expected to be FY23) on an EPS reported basis including the amortisation of intangibles recognised as a result of the acquisition based on a preliminary estimate of purchase price accounting.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

4. Full run rate annual pre-tax cost synergies of US$75 million expected to phase in over three years post acquisition close.

1 Strengthens CSL’s Value Driven Strategy

Combined CSL + Vifor Pharma Revenue (FY21)[1]

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Three Leading Segments

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Geographically Diverse Presence

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Veltassa
1% Other
ESA 5%
4%
Ferinject
5%
Immunoglobulins
35%
Sequirus
14% Revenue
US$12.3B
Other
3%
Albumin
9%
Specialty
Haemophilia 14%
9%
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Note: CHF converted to USD at average of daily FX for LTM period ending Jun-21 of 1.099. 1. Based on reported FY21 (June) for CSL. Vifor Pharma calendarised to LTM Jun-21.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

2 Builds a Significant Renal Franchise

Combined CSL and Vifor Pharma is a partner of choice in a growing renal market

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Estimated Renal Market Size [1]
US$ Billions ~$25bn+~$25bn+
~$13bn+~$13bn+
20202020 2020 26
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1. Source: Evaluate Pharma, Marketwatch, Center for Disease Control and Prevention, Nature.com, Grand View Research, PubMed.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

2 Renal Disease Represents a Large Growing Opportunity

Chronic Kidney Disease (CKD) is a leading cause of mortality and morbidity around the world

The prevalence of CKD has increased steadily over the past decade, with an annual growth rate of ~8%, largely driven by diabetes and high blood pressure

The need for dialysis is growing

~2 million patients worldwide receive dialysis, growing annually at 5–7%
360 people begin dialysis treatment for kidney failure every 24 hours
An estimated ~15% of adults suffer from CKD ( ~37 million ) in the U.S.
A substantial number of people lack access to kidney replacement therapy, and millions of people die of kidney failure each year, often without supportive care

Worldwide Kidney Disease and Dialysis Population Annual Growth Rate

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~8%~8%
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~5~5 - 7%7%
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Kidney Dis easeease

DialysiDialysi s

1. Based on estimated WW annual renal indication-related net sales.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

3 Complementary Portfolio Fit and Access to New Adjacencies

CSL Therapeutic Areas

CSL & Vifor Shared Disease Areas

Vifor Adjacent Disease Areas

Immunology

Anti-Neutrophil Cytoplasmic Autoantibody (ANCA) vasculitis Hidradenitis Suppurativa (HS) Complement-Mediated Diseases

Hematology

Sickle Cell Disease

Beta thalassemia

Transplant Delayed graft function

Hemodialysis (HD) – Major Adverse CV Events Iron Deficiency Cardiovascular & Diabetic Kidney Disease Patient Blood Management Metabolic Ischemic Stroke Heart Failure Ischemia/Reperfusion

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NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

3 CSL’s Rich Pipeline Aligns With Vifor’s Renal Framework

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CKD Complications AKI (Ischemia – Reperfusion) Dialysis
1
Vadadustat
INS-3001
Multiple Potential SNF-472
2
assets (Preclinical
& Clinical) 3
Vadadustat [4]
5
3
1
CSL964 CSL964
Sparsentan [6] GvHD treatment GvHD prevention
(Phase 3) (Phase 3)
7
CSL346 Clazakizumab
Diabetic kidney Ab-mediated
disease (Phase 2) rejection (Phase 3)
Preserving Renal Function Transplant
1. Licensed from F. Hoffman-La Roche AG. 5. Licensed from Cara Therapeutics, Inc.
22 2. Licensed from OPKO Health, Inc. 6. Licensed from Travere Therapeutics, Inc.
3. Licensed from Pfizer Inc. 7. Licensed from ChemoCentryx.
NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES 4. Licensed from Akebia Therapeutics, Inc., subject to certain conditions and pipeline assets
limited to selling Vadadustat to certain providers within the US dialysis market.
ESRD
ND-CKD
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3 Deep and Diverse Combined Pipeline

Deep an 3	d Diverse	Combine	d Pipelin	e	e
3 Partnered Projects Vifor Pharma pipeline Vifor Pharma responsible for development	PHASE I	PHASE II	PHASE III	REGISTRATION/ POST-REGISTRATION
	CSL324 (G-CSFR Antagonist mAb) HS	HIZENTRA® (SCIg) 20% Liquid SSc	Garadacimab (Anti-FXIIa mAb) HAE)	HAEGARDA® (C1-esterase inhibitor) HAE	AUDENZ™ (Adjuvanted Influenza Vaccine)
	CSL730 (rFC multimer)	Garadacimab (Anti-FXIIa mAb) ILD/IPF	EtranaDez (Gene therapy) Haem B	HIZENTRA® (SCIg) 20% Liquid	AFLURIA® QUAD (Egg-based Influenza Vaccine)
	CSL889 (Hemopexin) SCD	CSL346 (Anti-VEGFB mAb) DKD	KCENTRA® (4F-PCC) Trauma	PRIVIGEN® (IVIg) 10% Liquid	FLUAD®Trivalent (Adjuvanted Influenza Vaccine)
	CSL311 (Anti-Beta Common mAb)	Adjuvanted Cell Culture Influenza vaccine (aQIVc)	CSL112 (ApoA-1) ACS	IDELVION® (Rec rFIX-FP) Haem B	FLUAD®Quadrivalent (Adjuvanted Influenza Vaccine)
	CSL787 (Nebulized Ig)	Mavrilimumab (Anti-GM-CSFR mAb) GCA,COVID	Clazakizumab (Anti-IL-6 mAb) AMR	AFSTYLA® (Rec rFVIII) Haem A	FLUCELVAX® Quadrivalent (Cell-based Influenza Vaccine)
	ASLAN004 (Anti-IL-13R mAb) Atopic Dermatitis	Rayaldee® 1 (Oral calcifediol) COVID	CSL964 (Alpha Antitrypsin) Treatment of GvHD	ZEMAIRA® / RESPREEZA® Alpha-1 Antitrypsin	FOCLIVIA® / FOCETRIA Adjuvanted Egg-based influenza A (H5N1) Vaccine
	INS-3001 (oral calcification inhibitor) PAD, aortic valve stenosis	VIT-2763 Oral ferroportin inhibitor Sickle cell disease	CSL964 (Alpha Antitrypsin) Prevention of GvHD	PANVAX® Egg-based influenza vaccine	Vadadustat4 (oral HIF-PH inhibitor) Anemia CKD
	**Immunology	Haematology	Respiratory	Cardiovascular & Metabolic	Transplant
			Sparsentan2 (Dual ETA& AT1antagonist) FSGS	Korsuva3 (Kappa-opioid rec. agonist) CKD-aP	Rayaldee® 1 (oral calcifediol) Sec. hyperparathyroidism
			Sparsentan2 (Dual ETA& AT1antagonist) IgA Nephropathy	1. Licensed from OPKO Health,~~Inc.~~ 2. Licensed from Travere Therapeutics, Inc. 3. Licensed from Cara Therapeutics, Inc. 4. Licensed from Akebia Therapeutics, Inc., subject to certain conditions	~~Inc~~
			SNF-472 (Calcification inhibitor) CUA-ESRD
			SNF-472 (Calcification inhibitor)	~~limited to selling Vadadustat to certain providers within the US dialys~~ 5. Licensed from ChemoCentryx, Inc.
NOT FOR DISTRIBUTION OR RELEA	SE IN THE UNITED STATES		PAD-ESRD

4. Licensed from Akebia Therapeutics, Inc., subject to certain conditions and ~~limited to selling Vadadustat to certain providers within the US dialys~~ is market.

5. Licensed from ChemoCentryx, Inc.

4 Materially Enhances Scale and Free Cash Flow

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FY21 Revenue FY21 Free Cash Flow [2]
US$ Billions [1] US$ Billions [1]
+19% +20%
$12.3 $2.3 $2.4
$12.3
$10.3 $10.3 $2. 00 $$ 2. 00 $2.0 $2.0 $$ 0.4 $$ 0. 44
$10.3 $10.3 $2.0 $2.0
CSL’s Global Scale, R&D
Capabilities and Financial
Resources Enable the Pro
Forma Company to
Accelerate Growth in Key
Therapeutic Areas
CSL FY21 Vifor Pharma Combined FY21 CSL CSL FY21 Vifor Pharma Combined FY21 CSL
Standalone FY21 Standalone and Vifor Pharma Standalone FY21 Standalone and Vifor Pharma
CSL Vifor Pharma
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1. Vifor Pharma financials in CHF converted to USD at average of daily FX for LTM period ending Jun-21 of 1.099 and calendarised to June financial year end. 2. Free cash flow calculated as cash flow from operating activities less net capex, excluding synergies.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

5 Compelling Financial Profile

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Strong EPS Accretion

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Balance Sheet Flexibility Retained

Expected to be low-to-mid teens NPATA per share accretive in the first full year of CSL ownership[1] , including full run rate cost synergies[2]
Pro forma FY21 net debt / EBITDA of approximately 2.65x with clear de-leveraging profile
Balance sheet retains flexibility to support continued execution of R&D and expansion projects

2. Full run rate annual pre-tax cost synergies of US$75 million expected to phase in over three years post acquisition close.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

Transaction Funding

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NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

Transaction Funding

Transaction Funding Details

Tender Offer • The Tender Offer represents an aggregate equity value for Vifor Pharma of US$11.7 billion / A$16.4 billion
- The Transaction is to be funded via:
  - A Placement of A$6.3 billion (US$4.5 billion)
A fully committed debt bridge facility of US$6.0 billion / A$8.4 billion, to be replaced with longer term debt financing, including capital markets
Funding Existing cash / undrawn facilities of US$2.0 billion / A$2.8 billion
- CSL will also undertake a SPP to eligible CSL shareholders[1] in Australia and New Zealand. The SPP is targeting to raise up to A$750 million (US$534 million)

Sources and Uses[2]

Sources	US$bn	A$bn
Institutional Placement – Equity	4.5	6.3
Bridge Facilities – Debt	6.0	8.4
Existing Cash / Undrawn Facilities	2.0	2.8
Total Sources	12.5	17.5

Uses	US$bn	A$bn
Vifor Pharma Equity Value	11.7	16.4
Refinance of Vifor Pharma Indebtedness	0.6	0.8
Estimated Transaction Costs	0.2	0.3
Total Uses	12.5	17.5

Note: USD converted to AUD at spot FX of 1.406 and CHF converted to USD at spot FX of 1.083 as at 13 December 2021.

1. Eligible Shareholders are shareholders with a registered address in Australia or New Zealand and who are outside the United States on the register as at 7:00pm (AEDT) on Monday, 13 December 2021.

2. CSL will also undertake a non-underwritten SPP to eligible CSL shareholders, targeting to raise up to A$750 million (US$534 million).

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

Equity Raising Details

Placement and Share Purchase Plan Key Details

A fully underwritten institutional placement to eligible institutional investors to raise approximately A$6.3 billion (US$4.5 billion) ( Placement )
Offer Structure • A non-underwritten share purchase plan ( SPP ) targeting to raise up to A$750 million (US$534 million) • A$6.3 billion (US$4.5 billion) Placement
Placement Size • Issue of approximately 23.1 million new fully paid ordinary shares ( Placement Shares ), representing approximately 5.1% of current CSL ordinary shares on issue[1] • Placement price will be determined via a bookbuild process commencing at A$273.00 per share, representing a 8.2% discount to the last closing price of A$297.27 on 13
Placement Price December 2021
• Eligible institutional shareholders who bid at the final Placement Price for an amount less than or equal to their pro rata share of Placement Shares will be allocated their
Placement full bid, on a best endeavours basis[2] Allocation • Eligible professional and sophisticated shareholders[3] in Australia or New Zealand who wish to participate in the placement should contact their broker for further information. Priority will be given to broker bids that support existing shareholders
• Non-underwritten SPP to existing eligible CSL shareholders[4] in Australia and New Zealand ( Eligible Shareholders ), up to A$30,000 per Eligible Shareholder • The SPP is targeting to raise up to A$750 million (US$534 million) • The issue price per new fully paid ordinary share under the SPP ( SPP Shares ) will be the lower of the Placement Price and a 2.0% discount to the 5-day volume weighted average price ( VWAP ) of CSL shares up to and including the closing date of the SPP (currently scheduled for 7 February 2022), rounded to the nearest cent ( SPP Price )
• Any scale back of valid applications will be conducted having regard to the shareholdings of Eligible Shareholders (as at the record date of the SPP) who applied for new
SPP Overview shares in the SPP. The scale back methodology will ensure that, subject to the A$30,000 maximum application amount, participating shareholders will receive an amount of new shares that: at least maintains their percentage shareholding in CSL held prior to the announcement of the Placement and SPP (“Pro Rata Amount”); or is equivalent to their application if that is lower than their Pro Rata Amount
• CSL reserves the right to increase or decrease the size of the SPP at its discretion • An SPP offer booklet is expected to be sent to Eligible Shareholders, in accordance with their communications election, on Tuesday, 21 December 2021
Ranking • Placement Shares and SPP Shares will rank equally with existing CSL ordinary shares from their respective issue dates • The Placement is underwritten
Underwriting • The SPP is not underwritten

Note: USD converted to AUD at spot FX of 1.406 as at 13 December 2021.

1. Assuming a floor price of A$273.00 per Placement Share.

2. For this purpose, an eligible institutional shareholder’s ‘pro rata’ share of Placement Shares will be estimated by reference to CSL’s beneficial register on Monday, 13 December 2021, but without undertaking any reconciliation processes and ignoring shares that may be issued under the SPP. Unlike in a rights issue, this may not truly reflect the participating shareholder’s actual ‘pro rata’ share of Placement Shares. Nothing in this presentation gives a shareholder a right or entitlement to participate in the Placement and CSL has no obligation to reconcile assumed holdings (e.g. for recent trading or swap positions) when determining a shareholder’s ‘pro rata’ share of Placement Shares. Institutional shareholders who do not reside in Australia or other eligible jurisdictions will not be able to participate in the Placement – see “Appendix – International Offer Restrictions” for the eligible jurisdictions and relevant selling restrictions. CSL and the Joint Lead Managers disclaim any duty or liability (including for negligence) in respect of the determination of a shareholder’s ‘pro rata’ share of Placement Shares.

Either “professional investors” or “sophisticated investors” within the meaning of sections 708(11) and 708(8) of the Corporations Act 2001 (Cth) (“Corporations Act”) and “wholesale clients” under section 761G of the Corporations Act. Shareholders with a registered address in Australia or New Zealand on CSL’s share register at 7:00pm (AEDT) on Monday, 13 December 2021.

NOT FOR DISTRIBUTION OR RELEASE IN THE UNITED STATES

Equity Raising Timetable

Placement and Share Purchase Plan Timetable

Event	Date1 , 2
Record date for SPP	7:00pm (AEDT), Monday, 13 December 2021
Trading halt lodged	Prior to market open, Tuesday, 14 December 2021
Announcement of the Placement and SPP, Placement bookbuild opens	After market close, Tuesday, 14 December 2021
Placement bookbuild closes	Wednesday, 15 December 2021
Trading halt lifted	Thursday, 16 December 2021
Settlement of Placement Shares	Monday, 20 December 2021
Allotment and normal trading of Placement Shares commences	Tuesday, 21 December 2021
SPP offer opens and SPP offer booklet is made available	Tuesday, 21 December 2021
SPP offer closes	Monday, 7 February 2022
SPP issue and allotment date	Monday, 14 February 2022
Normal trading of SPP Shares commences	Tuesday, 15 February 2022
Dispatch of holding statements	Tuesday, 15 February 2022

1. The above timetable is indicative and subject to variation. CSL reserves the right to alter the timetable at its absolute discretion and without notice, subject to ASX Listing Rules and the Corporation Act and other applicable law.

All dates and times are Australian Eastern Daylight Time unless otherwise specified.