Bayer Pharmaceuticals

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39th Annual J.P. Morgan Healthcare Conference

Stefan Oelrich,

President Pharmaceuticals

January 13, 2021

Cautionary Statements Regarding Forward-Looking Information

This presentation may contain forward-looking statements based on current assumptions and forecasts made by Bayer management.

Various known and unknown risks, uncertainties and other factors could lead to material differences between the actual future results, financial situation, development or performance of the company and the estimates given here. These factors include those discussed in Bayer's public reports which are available on the Bayer website at http://www.bayer.com/.

The company assumes no liability whatsoever to update these forward-looking statements or to conform them to future events or developments.

Guidance at constant currencies, not including portfolio divestitures if not mentioned differently.

2J.P. Morgan Healthcare Conference, January 13, 2021

Driving Performance and Delivering New Growth Opportunities

Maximize the value of the existing portfolio

Exploit full potential of Xarelto and Eylea

Deliver on key pipeline assets

Three new potential blockbusters in Oncology, Cardiovascular and Women's Healthcare

Take advantage of breakthrough technologies

Expand into Cell & Gene Therapy

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After a Challenging Q2, V-shaped Recovery in Q3

Sales Growth vs Prior Year (cpa) by Quarter

5.3%

3.9%

5.9%

7.2%

-1.8% 3.9%

-8.8%

Q1

Q2

Q3

Q4

2019 2020

EBITDA margin before special items

34.1%

35.1%

33.3%

34.3%

33.3%

35.8%

29.9%

Q1

Q2

Q3

Q4

2019 2020

* Sales related growth rates are reported as currency and portfolio adjusted, and compared to the previous year

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  • Pharma business recovering in Q3 from Covid-19 impact
  • Xarelto´s growth trajectory intact (+13% YTD)
  • Stringent cost management to protect the bottom-line
  • Outlook for FY2020 confirmed on November 3, 2020:
    • Expected Sales growth: -1%
    • Expected underlying EBITDA margin: 34-35%

Increased Momentum to Deliver Innovation for Patients

Major achievements 2019/2020

Phase Transitions;

New Trials1

Finerenone HFmr/pEF

Aflibercept high dose nAMD & DME

Aflibercept retinopathy of prematurity

Regorafenib IO combi

Regorafenib glioblastoma

Factor XI portfolio

P2X3 inhibitor

PEG ADM inhale

Runaciguat

1 Key Phase II and III trials only

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Positive Phase III

Trial Results

  • Finerenone (FIDELIO-DKD)
  • Vericiguat (VICTORIA)
  • Copanlisib (CHRONOS-3)
  • Darolutamide (ARAMIS OS-data)
  • Rivaroxaban (PRONOMOS,
    VOYAGER PAD, EINSTEIN-Jr.)

Filings &

External

Approvals

Innovation

Darolutamide

BlueRock

Larotrectinib

AskBio

Vericiguat

KaNDy

Finerenone

Atara

Eylea PFS

Daré Bioscience

Rivaroxaban

investments

pediatric

A Successfully Matured Late-stage Pipeline that May Deliver Three New Potential Blockbusters

Nubeqa1 ̶AR-Antagonist

  • Launched in nmCRPC - global roll-out underway

Differentiated clinical profile - 31% OS benefit & favourable safety profile (ARAMIS)

Prim. completion of phase III trial in mHSPC mid-2021e (ARASENS)

  • Peak sales potential ≥€1bn

KaNDy NT-814 ̶Dual NK 1,3 Receptor-Antagonist

  • First-in-classoral, non-hormonal,once-dailyneurokinin-1,3 receptor antagonist
  • Positive phase IIb data for the treatment of frequent menopausal symptoms
  • Phase III to be initiated in 2021
  • Peak sales potential >€1bn

Finerenone ̶MR-Antagonist

  • Significant reduction of renal and cardiovascular outcomes in patients with CKD and T2D
  • Filed in key markets for CKD in T2D
  • Phase III trials in CKD/T2D (FIGARO) and in HFm/pEF (FINEARTS-HF) ongoing
  • Peak sales potential ≥€1bn

1In collaboration with Orion Corporation; 2In collaboration with Merck & Co. Inc., Kenilworth, NJ, USA

Vericiguat2 ̶sGC-Stimulator

  • Significant reduction of the combined risk of CV- death or HF-hospitalization in HFrEF-patients (VICTORIA)
  • Dosed on top of existing HF-therapies
  • Filed - FDA action date January 20, 2021
  • Peak sales potential ~€500m

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We Provide the Resources Needed for a Successful Commercialization of our Late-stage Pipeline Assets

Asset

Nubeqa1

Finerenone

KaNDy NT-814

Vericiguat2

Short- to mid-term Investment Areas

  • Continued global rollout in additional markets
  • Preparation for ARASENS readout
  • Continue to leverage positive OS data and differentiated safety profile
  • Preparation for potential first launches in 2021
  • Investing to re-enter the US-market in CV diseases
  • Preparation for FIGARO readout
  • Continuation of the HFm/pEF development program
  • Initiation of pivotal Phase III trial in 2021
  • Potential launches in first markets in 2021

1In collaboration with Orion Corporation; 2In collaboration with Merck & Co. Inc., Kenilworth, NJ, USA

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Increased Focus on External Innovation to Accelerate Replenishment of Pipeline and Broaden Modalities

Selected high-level overview

Momentum Significantly Increased

  • More than 20 Transactions signed in 2020
    • Deals covering the entire spectrum from equity investments (with LEAPS), over licensing agreements to acquisitions
    • Active portfolio management taking internal assets outside (e.g. Vincera Pharma)

Strategic Focus

  • Venturing into new modalities (Cell & Gene Therapy)
  • Broadening the Oncology pipeline (e.g. Systems Oncology, Atara)
  • Commercial partnerships in China (e.g. Hua Medicine)
  • Deals in the Digital Space (e.g. R&D: Schroedinger, Exscientia, Recursion; Commercial: One Drop)
  • Continued augmentation of core TAs: (WHC: KaNDy)
  • Strengthening the Cardiovascular pipeline (PeptiDream, Broad Institute)

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Our Cell & Gene Therapy Strategy Builds on Four Integrated Platforms to Drive the Next Wave of Innovation at Pharma

Gene Augmentation

Stem Cells

Allogeneic Cell Therapy

Collaboration with Atara

Biotherapeutics

  • Industry-leadingAAV vector gene augmentation platform
  • Monogenic & pathway diseases
  • CDMO business (Viralgen) already generates revenues
  • Creating induced pluripotent stem cells (iPSC) with broad differentiation
  • Create an entirely new generation of cellular medicines
  • IND for lead program in Parkinson's disease
  • Next-generation,mesothelin-directedCAR-T cell therapies
  • Focus on potential allogeneic, "off the shelf" tumor therapies

Gene Editing as cross-functional enabling technology

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Comprehensive Cell & Gene Therapy Pipeline that has Proven Ability to Yield Commercial Stage Assets

Project

Discovery

Preclinical

Phase I/II

Pompe Disease - Gene Therapy

Parkinson's Disease - Gene Therapy

Congestive Heart Failure - Gene Therapy

Factor VIII - Gene Therapy1

MSLN CAR-T Therapy (ATA2271)2

Parkinson´s Disease - Cell Therapy

MSLN CAR-T Therapy (ATA3271)2

> 15 preclinical assets

  • Comprehensive Cell & Gene Therapy pipeline established
  • Pipeline already comprises 6 clinical assets and multiple IND generating opportunities
  • AAV technology included in commercialized assets

1 In collaboration with Ultragenyx;

2 In collaboration with Atara Biotherapeutics

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Key Takeaways

1

We continue to maximize the value of the existing portfolio

2

Increased momentum to deliver innovation - late-stage pipeline may deliver three new

potential blockbuster products

3

We provide the resources needed for a successful commercialization of our late-stage

pipeline assets

4

Cell & Gene Therapy platform in place to drive the next wave of breakthrough innovation

5

C>-Pipeline established - 6 clinical assets and multiple IND generating opportunities

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Bayer Pharmaceuticals

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39th Annual J.P. Morgan Healthcare Conference

Stefan Oelrich,

President Pharmaceuticals

January 13, 2021

Abbreviations

AAV

Adeno-associated virus

IO

Immuno-oncology

AR

Androgen receptor

iPSC

Induced pluripotent stem cells

CAR-T

Chimeric antigen receptor modified T cells

mHSPC

Metastatic hormone sensitive prostate cancer

CDMO

Contract development and manufacturing organization

MRA

Mineralocorticoid receptor antagonist

CKD

Chronic kidney disease

nAMD

Neovascular age-related macular degeneration

C>

Cell and gene therapy

NK

Neurokinin

cpa

Currency and portfolio adjusted

nmCRPC

Non-metastatic castration resistant prostate cancer

CV

Cardiovascular

OS

Overall survival

DKD

Diabetic kidney disease

PAD

Peripheral artery disease

DME

Diabetic macula edema

PFS

Pre-filled syringe

EBITDA

Earnings before interest, tax, depreciation, and amortization

R&D

Research & Development

FDA

U.S. Food and drug administration

sGC

Soluble guanylate cyclase

HF

Heart failure

T2D

Type 2 diabetes mellitus

HFmrEF

Heart failure with mid-range ejection fraction

YTD

Year to date

HFpEF

Heart failure with preserved ejection fraction

HFrEF

Heart failure with reduced ejection fraction

IND

Investigational New Drug

13J.P. Morgan Healthcare Conference, January 13, 2021

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Bayer AG published this content on 13 January 2021 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 13 January 2021 13:11:02 UTC