Fourth quarter and full year 2023 results

R&D update Biopharma update Consumer Healthcare update
Growth engine Outlook 2024
Financial performance Appendices

Q4 2023 Results
Play to Win
February 1, 2024

3
Forward-looking statements
Investor Relations
This document contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-
looking statements are statements that are not historical facts. These statements include projections and estimates and their underlying
assumptions, statements regarding plans, business transformations, objectives, intentions and expectations with respect to future financial
results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking
statements are generally identified by the words “expects”, “anticipates”, “believes”, “intends”, “estimates”, “plans”, “potential”, “outlook”,
“guidance” and similar expressions. Although Sanofi’s management believes that the expectations reflected in such forward-looking statements
are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of
which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially
from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include
among other things, the uncertainties inherent in research and development, future clinical data and analysis, including post marketing,
decisions by regulatory authorities, such as the FDA or the EMA, regarding whether and when to approve any drug, device or biological
application that may be filed for any such product candidates as well as their decisions regarding labelling and other matters that could affect the
availability or commercial potential of such product candidates, the fact that product candidates if approved may not be commercially successful,
the future approval and commercial success of therapeutic alternatives, Sanofi’s ability to benefit from external growth opportunities, to
complete capital markets or other transactions and/or obtain regulatory clearances, risks associated with developing standalone businesses,
risks associated with intellectual property and any related pending or future litigation and the ultimate outcome of such litigation, trends in
exchange rates and prevailing interest rates, volatile economic and capital market conditions, cost containment initiatives and subsequent
changes thereto, and the impact that pandemics, political disruption or armed conflicts or other global crises may have on us, our customers,
suppliers, vendors, and other business partners, and the financial condition of any one of them, as well as on our employees and on the global
economy as a whole. The risks and uncertainties also include the uncertainties discussed or identified in the public filings with the SEC and the
AMF made by Sanofi, including those listed under “Risk Factors” and “Cautionary Statement Regarding Forward-Looking Statements” in Sanofi’s
annual report on Form 20-F for the year ended December 31, 2022. Other than as required by applicable law, Sanofi does not undertake any
obligation to update or revise any forward-looking information or statements.
Brand names appearing in this presentation are trademarks of Sanofi and/or its affiliates. Not all trademarks related to products under
development have been approved as of the date of this presentation by the relevant health authorities.

4
Agenda
Investor Relations
Launch engine to fuel
sustainable growth
Paul Hudson
R&D update
Houman Ashrafian
Biopharma update
Brian Foard, Thomas Triomphe,
Olivier Charmeil
Consumer Healthcare update
Julie Van Ongevalle
Financial performance
and outlook 2024
Jean-Baptiste de Chatillon
01
03
04
02
05

Launch engine to
fuel sustainable
growth

6
FY 2023: Launch performance and Dupixent drive strong growth
of Specialty Care and Vaccines
Investor Relations
All growth at CER unless footnoted. 1. Beyfortus, ALTUVIIIO, Tzield.
Specialty Care
€18.0bn
+14.2%
GenMed
€12.4bn
-7.1%
Vaccines
€7.5bn
+8.3%
€5.2bn
+6.3%
Consumer
Healthcare
Core assets
€6.3bn
+3.3%
• FY 2023 sales of €43.1bn
(+5.3%)
• Dupixent adding €2.8bn (at CER)
• More than offsetting the loss
of €1.1bn of Aubagio sales to
generics (LoE)
- FY 2023 sales growth w/o
Aubagio of 8.1%

7
Launch engine delivering
Investor Relations
1. Proprietary Specialty Pharmacy data and Sanofi analysis.
Protect all infants against RSV
in their first season
Strong ramp up in launch markets
Potential new standard
protection with weekly dosing
Leading share in switches1
in the U.S. at the end of Q4
First and only therapy to delay
onset of Type 1 diabetes
Expanding awareness and
screening programs
€731m
collectively
in first year
of launch
2023
2023 key launches far exceeded originally
communicated sales expectations of €400m
72
91
159
227
310
381
425
547
25
Beyfortus Nexviazyme Sarclisa Rezurock Cablivi
Altuviiio Xenpozyme Enjaymo Tzield
Total of >€2.2bn sales in 2023
from all Biopharma launches
combined (in €m)
2021 2022 2023

8
Building an Immunology Powerhouse driven by new launches,
Dupixent and Vaccines
Investor Relations
Barring unforeseen events. 1. Risk-adjusted net sales at CER, including Pharma already launched and Potential launches (tolebrutinib, itepekimab, amlitelimab, frexalimab, rilzabrutinib, lunsekimig, Oral TNFR1si).
Net
sales
in
€bn
Pharma launches
ALTUVIIIO, Cablivi, Enjaymo,
Nexviazyme, Tzield, Rezurock,
Sarclisa, Xenpozyme
Sanofi Vaccines
sales by 2030
>€10bn
2017 2018 2019 2020 2021 2022 2023 2024E 2030E
~€13bn
€10.7bn
€8.3bn
€5.2bn
€3.5bn
€2.1bn
€0.8bn
€0.2bn
Sales contribution
from Pharma launches
incl. pipeline by 20301
>€10bn
Reaching almost
€1.7bn of sales
in 2023
Low
double-digit
growth
(2023-2030
CAGR)
Vaccines GBU
Sales of €7.5bn
in 2023, including
>€500m in its
first year of launch

9
Preparing for the introduction of potential transformative COPD
therapies with an expected launch of Dupixent later this year
Investor Relations
1. G7 countries: U.S., France, Germany, Italy, Japan, UK, Canada; GOLD criteria Group E and uncontrolled with triple therapy or LAMA/LABA contraindicated to ICS. 2. Itepekimab not yet approved by any regulatory agency. 3. Dupixent is under
investigation and not yet approved for COPD and is being studied in patients with uncontrolled COPD treated with current SoC triple therapy among GOLD E. Patient populations exclude never smokers.
Patient population G71 – 2035e
itepekimab
First-in-class
anti-IL-33
2023 2024 2025
First-in-disease
U.S. submission EU submission CN submission
itepekimab2
~1,139K
patients
Dupixent®3
and
itepekimab2
~640K patients
Dupixent®3
only
~270K patients
Current
smokers
(30%)
Former
smokers
(70%)
Non-Type 2 Type 2
üüü
Boreas
Notus
Aerify 1
Aerify 2
Dupixent and itepekimab have the potential to
address different COPD populations with limited overlap
COPD peak sales potential for Dupixent
and itepekimab of >€5bn combined

10
Play to win priorities in 2024
Investor Relations
Dupixent is under investigation and not yet approved for COPD.
Launch
Excellence
Pipeline
Execution
Reallocation of pipeline
resources (i.e., from oncology
to immunology)
Centralization, hub strategy
Smart spending
Cost
Reallocation
Potential expansion
into COPD
Tolebrutinib
RMS/nrSPMS
Rilzabrutinib
ITP
18 Phase 2 and
12 Phase 3
starts

11
Advancing our commitments to address climate change and
leading the SMI Patient Care Pathways working group
Investor Relations
2023
2030
Carbon
neutrality
trajectory
2045
Net zero
emissions
-90% GHG reduction vs. 2019, across our operations (Scope 1&2)
and our entire value chain (Scope 3)
Reduce
GHG emissions
from our activities
(Scope 1&2)
Source
renewable
electricity
Expand
eco-car
fleet
Reduce
GHG emissions
from our activities
(Scope 3)
-38%
vs. 2019
-7%
vs. 2019
79%
vs. 2019
43%
vs. 2019
-55%
vs. 2019
-30%
vs. 2019
100%
vs. 2019
100%
vs. 2019
Patient Care Pathway aims to
reduce the carbon footprint of the
healthcare system and improve
health outcome.

R&D update

13
Outstanding pipeline news flow presented at the R&D Day
Investor Relations
lunsekimig
Demonstrated Proof of
Mechanism in Phase 1
study in Asthma
Dupixent
Positive Phase 3
results with
dupilumab in COPD
(BOREAS study)
itepekimab
Passed futility analysis
in COPD (AERIFY 1 &
2 studies)
frexalimab
Demonstrated 89%
reduction in new lesions
in Phase 2 study in
Multiple Sclerosis
amlitelimab
Primary endpoint met
in Phase 2 Atopic
Dermatitis study
PCV21 vaccine
Positive safety and
immunogenicity data
from the Phase 1/2
pediatric program
RSV toddler vaccine
Positive safety and
immune response data
from the Phase 1/2 trial
E. coli vaccine
Sanofi and JNJ announce
collaboration to
develop novel ExPEC
vaccine
TL1A
Sanofi and Teva announce
collaboration to deliver
inflammatory bowel
disease treatment
Oral TNFR1si
Demonstrated Proof
of Mechanism in
Phase 1 study in
Psoriasis
rilzabrutinib
Primary endpoints met
in Phase 2 CSU, with
improvements in other
secondary endpoints
Dupixent
Positive Phase 3 results
with dupilumab in COPD
(NOTUS study)
Sarclisa
Primary endpoints
met in Phase 3 1L
MM (IMROZ study)
R&D Day
December
2023

H1 2024 H2 2024
Dupixent
COPD U.S./EU Approval
CSU (Study C) Pivotal trial readout
tolebrutinib
RMS (GEMINI 1/2) Pivotal trial readout
nrSPMS (HERCULES) Pivotal trial readout
amlitelimab Asthma Phase 2 readout
rilzabrutinib
ITP (LUNA 3) Pivotal trial readout
Asthma Phase 2 readout (HD)
Sarclisa
1L MM Ti (IMROZ) U.S. Submission
SubQ 2/3L MM (IRAKLIA) Pivotal trial readout
14
Expected major R&D milestones in 2024
Investor Relations
As of December 31, 2023, barring unforeseen events. For abbreviations see slide 61.

Ph2
amlitelimab HS
lunsekimig Asthma
Oral TNFR1si Psoriasis
Oral TNFR1si RA
frexalimab T1D
amlitelimab SSc
SP0256 RSV OA Combo
Barring unforeseen events. .
15
Ph3
amlitelimab AD
frexalimab RMS
frexalimab nrSPMS
Dupixent Asthma ped
SP0125 RSV toddler
riliprubart CIDP Refractory
riliprubart CIDP IVIg treated
Investor Relations
Ph2
amlitelimab Celiac
amlitelimab AA
lunsekimig AD
lunsekimig Asthma high risk
lunsekimig CRSwNP
Oral TNFR1si IBD
Ph3
rilzabrutinib CSU
rilzabrutinib PN
SAR443820 ALS
SP0202 PCV21 pediatric
SP0218 Yellow fever
H1 H2
15
Unprecedented pipeline of blockbuster opportunities
Starting multiple Phase 3 and Phase 2 projects in 2024
First-patient in achieved
>35 Phase 3 projects in pipeline by 2025

Peak investment
Multiple Phase 3 trials
launching in parallel
Focus
Breadth of platforms,
sites and therapeutic areas
Pipeline sustainability
Fueled by in-house research
and external innovation
16
Key topics to prepare for the future
Investor Relations

Strategic fit
17
INBRX-101 acquisition to add innovative asset with blockbuster
potential to rare disease portfolio addressing AAT deficiency
Investor Relations
Acquisition subject to customary closing conditions.
INBRX-101
• Adding mid-stage asset in Rare Diseases
• Expansion of our immune-mediated respiratory portfolio
Unmet need
Differentiated
clinical data
• Recombinant AAT Fc with potential best-in-class profile
• Ph1 trial completed, achieving normal AAT levels
• Potential for less frequent dosing and favorable safety
profile, improving SOC plasma-derived AAT therapy
• Fast Track designation by FDA in AATD in May 2023
• Proven mechanism of action with Ph2b data in H2 2025,
potential for accelerated approval
• Potential eligible U.S. diagnosed patient population 20-35k
• Potential eligible EU diagnosed patient population 15-25k
Blockbuster
potential

Biopharma
update
Q4 2023
Vaccines
Specialty Care GenMed

Specialty Care performance
Investor Relations
Dupixent
€2,990m
+31.3%
Rare Diseases1
€1,266m
+14.5%
€4.7bn sales +13.7%
Neurology,
Oncology &
Rheumatology
€458m
-39.5%
Dupixent
Continued strong demand-driven growth in
approved indications across all geographies
Rare Diseases
• ALTUVIIIO launch execution and Alprolix
performance drive double-digit growth of
hemophilia franchise
• Robust growth of all ERT franchises supported
by new patient accruals and continued launch
rollout of Nexviazyme and Xenpozyme
• Aubagio LoE sales erosion with full quarter
of exposure to generics in the U.S. and Europe
19
Q4 2023
All growth at CER unless footnoted. Growth rate is vs. Q4 2022.
1. Rare Diseases includes Rare Blood Disorders.
Vaccines

20
Dupixent strong performance in 2023; expected to deliver
~€13bn in 2024
Investor Relations
1. All percentage growth at CER. 2. IQVIA, Dec 2023.
Global Dupixent sales (in € m)
U.S.
(+28%)1
Ex-U.S.
(+43%)1
1,170
Q1 Q2 Q3 Q4
2,402 2,316
2,562
2,847
2,990
6,346
8,145
1,947
2,570
2022 2023
8,293
10,715
+34%1
2023
FY performance highlights
Recent progress
• Worldwide growth of +34%, with each
major geography (U.S., Europe, RoW region)
exceeding >30% growth
• #1 U.S. NBRx share in all 5 approved indications2
• COPD submission completed (EU, U.S., CN)
• Asthma approved in China
• U.S. AD label update unique hand
and/or foot atopic dermatitis efficacy
and safety data
2022
Q4
Ex-U.S. U.S.
2,299
691
Vaccines

21
Top choice for switches driven by efficacy profile
Investor Relations
1. Proprietary Specialty Pharmacy data and Sanofi analysis. 2. Including patients on free trials.
Cumulative patient number
with ALTUVIIIO Prescription2
Accelerating ALTUVIIIO U.S. launch performance
Q2 Q3 Q4
2023
250
1,100+
Strong switch dynamics
Capturing >50% of switches1 in total U.S.
hem A market, up from 40% at the end of Q3
Growing overall portfolio
~2/3 of switches from competition
Expansion ex-U.S.
Rapid Japan uptake with >30 patients
in first few weeks of launch in late Q4
650+
Vaccines

Booster vaccines
€139m
-1.4%
Meningitis,
Travel &
Endemic
€242m
+10.4%
22
Vaccines performance
Investor Relations
Polio/
Pertussis/Hib
€434m
+3.4%
Influenza
€741m
-4.0%
Others
€20m
-76.1%
€2.0bn +21.1%
sales
Significant contribution from Beyfortus uptake
due to “All Infant Protection” recommendation
in launch countries (U.S., France and Spain)
Influenza sales reflect lower immunization
rates and increased U.S. competition
Meningitis and PPH franchises benefited
from public order pattern in the quarter
RSV
€410m
Q4 2023
Vaccines

11% 10%
38%
PCV Rotavirus Beyfortus
Beyfortus – unprecedented pediatric immunization uptake
Beyfortus lays foundation for best-in-class RSV portfolio
• Successful implementation
for broad infant population
with high immunization rates
- ~35% in the U.S. and France
- 90% in Spain, with real-world
evidence data from Galicia1
showing significant
hospitalization reduction
• Harmonie Ph3b results
published in NEJM2
23
• U.S. Fast Track Designation in Oct 2023
• Phase 1/2 RSV-hMPV initiated in Nov
2023
• U.S. Fast Track Designation in
2020 and EU PRIME in Dec 2023
• Phase 3 start in Q1 2024
RSV Toddler for 2nd season onwards
RSV Older Adult combination
Investor Relations
23
RSV new development
Beyfortus launch
Innovative vaccines for all target populations
1. (NIRSE-GAL study: evolution of Immunization Coverage with nirsevimab (nirsegal.es)). 2. https://www.nejm.org/doi/full/10.1056/NEJMoa2309189.
U.S. uptake in the first 6 months
surpasses previous pediatric
immunization benchmarks
PCV (Prevnar) and Rotavirus (Rotateq) data from IQVIA DDD for
private doses, and CDC data for public doses. Beyfortus 2023-
2024 season immunization rates projected from sales data, to be
confirmed after RSV season
Vaccines

24
GenMed performance
Investor Relations
€3.0bn -2.4%
sales
Industrial
sales
€176m
+1.1%
Core assets
€1,576m
+6.3%
Non-core
assets
€1,252m
-11.6%
Core assets
• Growth of 6.3% in Q4 2023
• Continued expansion of Rezurock offset by
Mozobil LoE in the U.S.
• Robust growth of Toujeo, Plavix in China
and Praluent in EU
Non-core assets
• Lantus impacted by significant U.S. net price
decline due to unfavorable channel mix and
VBP China
Portfolio streamlining
• Portfolio streamlining impact sales -2.6ppt
(around €87m)
Q4 2023
Vaccines

25
TZIELD - a catalyst for change within Autoimmune T1D
Investor Relations
1. Captures net sales after April 27, 2023 (6m in Q2, 9m in Q3, 10m in Q4). 2. Testing of 3+ autoantibodies Nov 2023 YTD vs. Nov 2022 YTD.
• 168 people infused
with TZIELD
+25% growth
(Q4 vs. Q3), time to
infusion around 30 days
• 216m U.S. lives
covered in plans
Since acquisition
€25m sales1
Solid early
performance
Screening
accelerates
• National screening
campaign launched
in Times Square
Screening grew
+31% driven
by endocrinologists2
• ADA guidelines
updated
Recommend T1D
family screening
TZIELD label expansion
and new horizons in aT1D
• Regulatory
interaction with
FDA & EMA in Q1'24
FPI for the Phase 2
frexalimab study
T1D indication
The 1 Pledge launch in Times
Square (U.S.) with Grammy Awards
winner Usher
Vaccines

Consumer
Healthcare
update
Q4 2023
R&D update Consumer Healthcare update
Biopharma update

27
CHC performance
Investor Relations
All growth at CER. Growth rate is vs. Q4 2022. Organic growth: Excluding impacts of divestments & acquisitions.
€1.2bn sales +8.5%
Physical
& Mental
Wellness
€182m
+58.4%
Others
€164m
-11.2%
Cough & Cold
€125m
-0.8%
Digestive Wellness
€322m
+18.5%
Allergy
€147m
-5.4%
Pain Care
€275m
+1.0%
11th
consecutive growth quarter
• Growth supported by price
• Digestive Wellness continues to outperform
• Physical & Mental Wellness category driven by
Qunol acquisition in the quarter
15 Priority Brands continuing to contribute
to the majority of our growth
Q4 organic growth +4.8%
Q4 2023

28
Dulcolax: Category leader repeatably performing above market
Investor Relations
1. IPSOS U&A 2023. 2. IPSOS Fast Facts Survey 2023. 3. By U.S. Pharmacists - Newsweek, 2023. 4. Consumer Survey of Product Innovation 2023. 5. Global sinergi database; OTC+RX market definition; all countries ex CHN, MR Nov 23.
Gentler
formats
successful
innovation
Global
brand
Strong
reputation
By U.S. Consumers for
DULCOLAX® Chewy Fruit Bites4
Attractive under-
penetrated market
Empowering
self-care,
breaking
taboo
Above
market
growth
for 3+
years5
80+
countries
~1/3
WW population
suffers from
constipation1
50%
not treated with
laxatives2
3

Financial
performance
Q4 2023
R&D update Consumer Healthcare update
Biopharma update

30
Q4 2023 performance
Investor Relations
All growth at CER unless footnoted.
• Q4 sales up 9.3%
• Double-digit growth of Specialty
Care driven by Dupixent and
Rare Diseases
• Beyfortus uptake drives
strong quarter for Vaccines
• GenMed anticipated deceleration
of decline with U.S. glargine
business still down double-digit
• CHC growth from key categories
and acquisition (Qunol)
€4.7bn
+13.7%
€3.0bn
-2.4%
€2.0bn
+21.1%
Core assets
€1.6bn
+6.3%
€1.2bn
+8.5%
Consumer
Healthcare
Vaccines

31
Q4 Group P&L
Investor Relations
All growth at CER. 1. Margin at published rate.
31
Sales growth
+9.3%
Gross margin
+2.8ppt, due to product
mix and COVID-19 vaccine
revenues
BOI margin
-1.7ppt (at published rates)
mainly due to a decrease
in capital gains related to
product disposals as compared
to the same quarter of last year
€m Q4 2023 Q4 2022 % Change
Net Sales 10,919 10,725 +9.3%
Other revenues 1,282 731 +90.8%
Gross profit 8,167 7,722 +13.5%
Gross margin % 74.8%1 72.0%1
R&D (1,872) (1,823) +6.6%
SG&A (2,931) (2,895) +7.4%
Operating Expenses (4,803) (4,718) +7.1%
Other current operating income & expenses (821) (276) +219.6%
Business Operating Income 2,583 2,724 +5.3%
Business operating margin 23.7%1 25.4%1
Effective tax rate 18.1% 20.6%
Total Business Net Income 2,083 2,141 +8.2%
Average number of shares 1,253.6 1,254.0
Business EPS 1.66 1.71 +8.2%

32
FY 2023 Group P&L
Investor Relations
32
Sales growth
+5.3%
Gross margin
+1.1ppt, of which 0.8ppt
due to COVID-19 vaccine
related sales and revenues
(non-recurring)
BOI margin
-0.9ppt (at published rate)
due to currency, stable at CER
EPS
+5.4%, in-line
with guidance
€m FY 2023 FY 2022 % Change
Net Sales 43,070 42,997 +5.3%
Other revenues 3,374 2,392 +50.0%
Gross profit 32,228 31,697 +7.0%
Gross margin % 74.8%1 73.7%1
R&D (6,728) (6,706) +3.0%
SG&A (10,692) (10,492) +6.1%
Operating Expenses (17,420) (17,198) +4.9%
Other current operating income & expenses (2,224) (1,514) +55.9%
Business Operating Income 12,670 13,040 +4.3%
Effective tax rate 18.8% 19.3%
Total Business Net Income 10,155 10,341 +5.5%
Average number of shares 1,251.7 1,251.9
Business EPS 8.11 8.26 +5.4%

33
Proposed dividend of €3.76
Investor Relations
Subject to AGM’s approval on April 30, 2024.
1994 2023

Outlook
2024

35
Strategic cost initiatives, targeting total up to €2bn from 2024
to end of 2025, to be reallocated in majority
Investor Relations
Priorities
In pursuit of first-in-class/
best-in-class pipeline assets,
active reallocation of
pipeline resources
(e.g., from oncology
to immunology)
Smart
spending
Further leverage
procurement to generate
additional savings
Operational
excellence
Optimize country setup,
increase degree of
centralization by expanding
hub strategy, refocus
R&D infrastructures and
technology platforms
€0.7bn
€0.6bn
€0.7bn

36
Expected business dynamics in 2024 with Q1 marked by
high base of comparison
Investor Relations
Barring unforeseen events.
FY 2024 Q1 2024
Sales • Dupixent expected to reach approximately €13bn
• Vaccines sales expected to grow mid-single-digit
• Aubagio LoE impact, mainly in H1
• GenMed divestment impact of ~€300m
• Dupixent annual step-up in U.S. copay assistance program
• High rate of Aubagio generic erosion in U.S. and Europe
• High base in Vaccines due to 2023 COVID-19 vaccine sales
(€167m in Q1 2023)
• Limited supply of Beyfortus
• High base of Lantus in the U.S. in Q1 2023
(versus Q2, Q3 and Q4 2023)
P&L • Gross margin slightly declining
• OPEX growth due to step-up in development spending
• Capital gains from product divestments expected >€500m
• Tax rate of 21% (vs. 18.8% in 2023)
• No COVID-19 vaccine revenues (€62m in Q1 2023)
• OPEX growth due to increase in development spending
• High capital gains from product divestments (€307m)
in Q1 2023
• Tax rate of around 21% (vs. 19.0% in Q1 2023)

37
FY 2024 guidance
Investor Relations
Barring unforeseen events. 1. Based on January 2024 average rates.
37
approximately
-3.5% to -4.5%
Currency
impact1
EPS growth
Low single-digit
EPS decline
(roughly stable
at comparable
tax rate)

Q&A session

R&D
appendices
Financial appendices ESG appendices Abbreviations Collaborations
R&D appendices

Investor Relations
As of December 31, 2023.
Near-term milestones of our development pipeline
H1 2024
rilzabrutinib ITP Ph3
venglustat GM2 Gangliosidosis Ph3
frexalimab SjS Ph2
SAR443820 (RIPK1i) ALS Ph2
rilzabrutinib Asthma HD Ph2
H2 2024
Dupixent CSU Ph3
Dupixent BP Ph3
Dupixent CPUO Ph3
Sarclisa Subcutaneous Ph3
tolebrutinib RMS Ph3
tolebrutinib SPMS Ph3
amlitelimab Asthma Ph2
Anti-TL1A IBD IA Ph2
rilzabrutinib IgG4-RD Ph2
rilzabrutinib wAIHA Ph2
40
2025
itepekimab COPD Ph3
tolebrutinib PPMS Ph3
amlitelimab HS Ph2
eclitasertib UC Ph2
frexalimab SLE Ph2
IRAK4 degrader AD Ph2
IRAK4 degrader HS Ph2
Oral TNFR1si RA Ph2
Oral TNFR1si PSo Ph2
TNFa/OX40L HS Ph2
40
R&D appendices

41 Investor Relations
As of December 31, 2023. For abbreviations see slide 61. For collaborations see slide 62.
1. Also known as SAR441344. Dupixent COPD sBLA submission completed in December 2023.
R&D Pipeline Registration & Phase 3
Immunology & Inflammation
DupixentA
Anti-IL-4/IL-13 mAb
Bullous Pemphigoid
Chronic Pruritus of Unknown Origin
Chronic Spontaneous Urticaria
Eosinophilic Gastritis
itepekimabA Anti-IL-33 mAb Chronic Obstructive Pulmonary Disease
amlitelimab Anti-OX40L mAb Atopic Dermatitis
Neuro-inflammation
tolebrutinib BTK inhibitor
Relapsing Multiple Sclerosis
Primary Progressive MS
Non-relapsing Secondary Progressive MS
frexalimabB,1 Anti-CD40L mAb
Relapsing Multiple Sclerosis
Non-relapsing Secondary Progressive MS
Rare Diseases
Nexviazyme Enzyme Replacement Therapy (GAA) Pompe Disease Infantile Onset
venglustat Oral GCS inhibitor
Fabry Disease
Gaucher Disease Type 3
GM2 Gangliosidosis
fitusiran RNAi targeting anti-thrombin
Hemophilia A and B
Hemophilia A and B pediatric
rilzabrutinib BTK inhibitor Immune Thrombocytopenia
Vaccines
MenQuadfi Meningococcal ACWY conjugate vaccine Meningitis 6w+ (U.S./EU)
SP0087 Purified vero cell rabies vaccine Rabies
SP0282C 9-valent Extraintestinal Pathogenic E. Coli
vaccine (ExPEC9V)
Invasive ExPEC disease
Oncology
Sarclisa
Anti-CD38 mAb + combinations
1L Newly Diag. MM Ti (IMROZ)
1L Newly Diag. MM Te (GMMG)
Smoldering MM (ITHACA)
Anti-CD38 mAb SubQ. + combinations 2/3L Relapsed, Refractory MM (IRAKLIA)
Phase 3
Registration
Transplant & Type 1 Diabetes
Rezurock ROCK2 inhibitor
Chronic Lung Allograft Dysfunction
1L chronic Graft-Versus-Host Disease
TZIELD Anti-CD3 mAb Type 1 Diabetes
DupixentA
Anti-IL-4/IL-13 mAb Chronic Obstructive Pulmonary Disease
KevzaraA
Anti-IL-6 mAb Polyarticular Juvenile Idiopathic Arthritis
R&D appendices

1. Also known as SAR441344. 2. Also known as SAR443765. 3. Also known as SAR443122/DNL758. 4. Also known as KT474. 5. Also known as TEV’574. 6. Also known as SAR445088. 7. Also known as DNL788. 8. Also known as SP0178.
NANOBODY is a trademark of Sanofi and affiliates.
R&D Pipeline Phase 2
Rare Diseases
riliprubart6
Complement C1s inhibitor Cold Agglutinin Disease
rilzabrutinib BTK inhibitor Warm Autoimmune Hemolytic Anemia
SAR442501 Anti-FGFR3 Ab Achondroplasia
Oncology
Sarclisa Anti-CD38 mAb + combinations Relapsed, Refractory MM
DupixentA Anti-IL-4/IL-13 mAb Ulcerative Colitis
amlitelimab Anti-OX40L mAb
Asthma
Hidradenitis Suppurativa
rilzabrutinib BTK inhibitor
Asthma
Chronic Spontaneous Urticaria
IgG4-related disease
frexalimabB,1
Anti-CD40L mAb
Sjogren’s Syndrome
Systemic Lupus Erythematosus
SAR441566 Oral TNFR1 signaling inhibitor
Psoriasis
Rheumatoid Arthritis
lunsekimig2 Anti-IL-13/TSLP Nanobody® VHH Asthma
eclitasertibD,3
RIPK1 inhibitor Ulcerative Colitis
SAR444656E,4 IRAK4 degrader
Atopic Dermatitis
Hidradenitis Suppurativa
SAR442970 Anti-TNFa/OX40L Nanobody® VHH Hidradenitis Suppurativa
SAR447189F,5 Anti-TL1A mAb
Crohn’s Disease
Ulcerative Colitis
Neuro-inflammation
riliprubart6 Complement C1s inhibitor CIDP
SAR443820D,7 RIPK1 inhibitor
Amyotrophic Lateral Sclerosis
Multiple Sclerosis
Transplant & Type 1 Diabetes
frexalimabB,1 Anti-CD40L mAb Type 1 Diabetes
riliprubart6
Complement C1s inhibitor Antibody-Mediated Rejection
Vaccines
Fluzone HD8 Inactivated Influenza Vaccine (IIV) Pediatric Influenza
SP0218 Vero cell Yellow Fever vaccine Yellow fever
SP0202G
21-valent Pneumococcal conjugate vaccine Prevention of pneumococcal disease
SP0230 Multicomponent Meningococcal vaccine Meningitis B
SP0256 mRNA RSV vaccine RSV older adult
SP0125 Live attenuated virus RSV vaccine RSV toddler
R&D appendices

1. Also known as ABL301. 2. Also known as KDS1001. 3. Also known as KD050. 4. Also known as AMX-818. 5. Also known as SAR444245/THOR707. NANOBODY is a trademark of Sanofi and affiliates.
R&D Pipeline Phase 1
Rare Diseases
SAR443809 Anti-Factor Bb mAb Rare renal diseases
SAR439459 Anti-TGFb mAb Osteogenesis Imperfecta
SAR444836I
PAH replacement AAV-based gene therapy Phenylketonuria
Oncology
SAR444881J
Anti-ILT2 mAb Solid tumors
SAR4454192
NK-Cell-based immunotherapy Acute Myeloid Leukemia
SAR4458773 Anti-PD1/IL-15 fusion protein Solid tumors
SAR443579K
Trifunctional anti-CD123 NK-Cell engager Acute Myeloid Leukemia
SAR445514K Trifunctional anti-BCMA NK-Cell engager Relapsed, Refractory MM
SAR4463094
HER2 T-Cell engager Solid tumors
SAR444200 Anti-GPC3/TCR Nanobody® VHH Solid tumors
SAR445953L Anti-CEACAM5/Topo1 ADC CRC
pegenzileukin5 Non-alpha IL-2 SynthorinTM molecule
(dose optimization)
Solid tumors
SAR444336 Non-beta IL-2 SynthorinTM
molecule Inflammatory indication
SAR444559 Anti-CD38 mAb Next Generation Inflammatory indication
SAR445611 Anti-CX3CR1 Nanobody® VHH Inflammatory indication
SAR445399 Anti-IL1R3 mAb Inflammatory indication
SAR446422 Anti-CD28/OX40 bispecific Ab Inflammatory indication
Neuro-inflammation
SAR446159H,1 Anti-Synuclein/IGF1R mAb Parkinson’s disease
Vaccines
SP0273 mRNA Quadrivalent Influenza Vaccine (QIV) Influenza
SP0256 mRNA RSV combination vaccine Multiple infections older adult
SP0230 Meningococcal ABCWY conjugate vaccine Meningitis
R&D appendices

2024
tolebrutinib
RMS
rilzabrutinib
ITP
tolebrutinib
nrSPMS
fitusiran
Hemophilia A/B
Sarclisa
1L Newly Diag. MM Ti
(IMROZ)
venglustat
GM2 gangliosidosis
MenQuadfi
6w+
44
As of December 31, 2023. Excluding Phase 1 and 2 (without Proof of Commercial Concept) and selected submissions. Projects within a specified year are not arranged by expected time of submission.
Expected submission timelines
44
2026 and beyond
Dupixent
CPUO
venglustat
Gaucher Type 3
amlitelimab
Atopic Dermatitis
fitusiran
Hemophilia A/B ped
frexalimab
RMS
Sarclisa
Smoldering MM
frexalimab
nrSPMS
SP0282
Invasive ExPEC disease
riliprubart
SOC-Refractory CIDP
SP0125
RSV toddler
riliprubart
IVIg-Treated CIDP
SP0202
Prevention of pneumococcal
disease
SP0218
Yellow fever
2025
Dupixent
CSU
Nexviazyme
Pompe Disease Infantile Onset
Dupixent
Bullous pemphigoid
venglustat
Fabry Disease
itepekimab
COPD
Sarclisa SubQ
3L RR MM (IRAKLIA)
tolebrutinib
PPMS
Sarclisa
1L Newly Diag. MM Te
(GMMG)
SP0087
Purified vero rabies vaccine
Investor Relations
R&D appendices

Financial
appendices
R&D appendices

GenMed Q4 2023 core assets performance
Core asset sales (in € million)
289
272
245 250
104 96
55
263
278
254
231
87
118
61
-0.3% +11.4%
+13.1% -0.4%
-12.5% +26.0%
+18.2%
Q4 2022 Q4 2023
R&D appendices

Q4 main product sales
Q4 2023 sales (€m) Growth
Dupixent 2,990 31.3%
Influenza vaccines 741 -4.0%
Polio/Pertussis/Hib vaccines 434 3.4%
Beyfortus 410 -
Toujeo 278 11.4%
Lantus 277 -24.9%
Lovenox 263 -0.3%
Plavix 254 13.1%
Meningitis, Travel and Endemic vaccines 242 10.4%
Fabrazyme 242 9.2%
Myozyme 160 -20.4%
Alprolix 142 6.4%
Booster vaccines 139 -1.4%
Cerezyme 134 5.0%
Nexviazyme 131 +115.4%
Aubagio 121 -74.0%
Praluent 118 26.0%
Thymoglobulin 112 5.1%
Aprovel 106 7.7%
Kevzara 105 41.8%
R&D appendices

FY 2023 main product sales
FY 2023 sales (€m) Growth
Dupixent 10,715 34.0%
Influenza vaccines 2,669 -5.5%
Polio/Pertussis/Hib vaccines 2,165 -0.1%
Lantus 1,420 -32.3%
Meningitis, Travel and Endemic vaccines 1,170 0.5%
Lovenox 1,125 -8.7%
Toujeo 1,123 6.2%
Fabrazyme 991 11.2%
Aubagio 955 -52.6%
Plavix 948 4.4%
Myozyme 783 -15.1%
Cerezyme 687 9.1%
Booster vaccines 598 5.1%
Beyfortus 547 -
Alprolix 540 11.3%
Thymoglobulin 478 14.1%
Eloctate 471 -15.5%
Nexviazyme 425 126.0%
Praluent 422 15.2%
Aprovel 417 -8.8%
R&D appendices

nirsevimab/Beyfortus
Initial agreement Sanofi-AstraZeneca (March 2017)
Major markets (U.S., FR, DE, ES, IT, UK, JP) Rest of world markets
Net sales Sanofi consolidates worldwide net sales
Cost of sales Sanofi consolidates worldwide cost of sales (finished goods purchased from AstraZeneca)
R&D AstraZeneca & Sanofi share the alliance development costs 50/50
SG&A
Sanofi expenses 100% of its SG&A (and further shares 50/50
in OOIE)
Sanofi expenses 100% of its SG&A
(not shared)
Other operating
income and expenses
Alliance
profit & loss
Sanofi shares with AstraZeneca the alliance commercial
profit & loss 50/50
Sanofi pays to AstraZeneca
25% of net revenues
Intangible asset
Beyfortus
(amortized below
BNI over useful life)
Upfront EUR 120m paid by Sanofi to AstraZeneca upon closing (March 2017)
Regulatory
milestones
AstraZeneca received from Sanofi EUR 55m and will receive EUR 65m for BLA Approval in the U.S.
Sales
milestones
AstraZeneca to receive up to EUR 375m sales milestones from Sanofi, upon achievement of certain sales related milestones
Above BNI Below BNI
R&D appendices

Sanofi accounting of nirsevimab/Beyfortus
Updated and new agreements Sanofi-AstraZeneca and Sanofi-Sobi (April 2023)
U.S. Major markets (CN, FR, DE, ES, IT, UK, JP) Rest of world markets
Net sales Sanofi consolidates worldwide net sales
Cost of sales Sanofi consolidates worldwide cost of sales (finished goods purchased from AstraZeneca)
R&D Sanofi bears 100% of the costs from April 2023 onward AstraZeneca & Sanofi share the alliance development costs
SG&A Sanofi bears 100% of the costs from April 2023 onward Sanofi expenses 100% of its SG&A
(and further shares 50/50 in OOIE)
Sanofi expenses 100% of
its SG&A (not shared)
Other
operating
income and
expenses
Alliance profit
& loss
Sanofi consolidates 100% of the economics in the U.S. from
April 2023 onward
Sanofi shares with AstraZeneca the alliance
commercial profit & loss 50/50
Sanofi pays to AstraZeneca
25% of net revenues
Intangible
asset
Beyfortus
(amortized
below BNI
over useful
life)
Upfront EUR 120M paid by Sanofi to AstraZeneca upon closing (March 2017)
Regulatory milestones AstraZeneca received from Sanofi EUR 120m
Sales milestones AstraZeneca to receive up to EUR 375m sales milestones from Sanofi, upon achievement of certain sales related milestones.
A first sales milestone of EUR 25m was triggered in Q4 2023
Additional rights
from AstraZeneca
(amendment April 2023)
Sanofi records price of U.S rights to obtain full commercial control (Fair Value)
Royalty Agreement Sanofi–Sobi (April 2023)
Financial liability (Sobi) Initial recognition at Fair Value of U.S. royalties due to Sobi - Liability reduced by royalty payments over time -
Subsequent re-measurement in P&L below BNI
Updated agreement Sanofi-AstraZeneca
Above BNI Below BNI
R&D appendices

Investor Relations
Q4 sales and EPS
Currency impact
Company sales Business EPS
€1,108m
€475m
€16m
€-484m
€-922m €-799m
+0.31
2022
+0.09
Q3 Q4
-0.01
Q1
2023
Q2
-0.13
51
Q3
-0.27
-0.19
2022
Q3 Q4 Q1
2023
Q2 Q3
Q4 Q4
R&D appendices

Investor Relations
1. Credit ratings reaffirmed: Moody’s A1/stable, S&P AA/stable, Scope AA/stable as of December 31, 2023. 2. Including derivatives used to manage net debt: €142m at December 31, 2022, and €111m at December 31, 2023.
3. Effective January 1, 2019, net debt does not include lease liabilities following the first-time application of IFRS16. 4. Including €593m use of funds from acquisition of treasury shares, -€195m of issuance of Sanofi shares and €498m of other items.
-997
896
1,113
1,236
4,454
Dividends paid
to shareholders
of Sanofi
6,437
-9,830
4,484
7,793
Net Debt
December 31,
20222,3
Net Debt
December 31,
20232,3
FCF before
restructuring,
acquisitions
& disposals
Proceeds
from
disposals
Asset
acquisition
Restructuring
& similar
items
Other4
Net debt evolution in 20231
€ millions
52
Acquisitions of
investments in
consolidated
undertakings
R&D appendices

Q4 CHC P&L
53
€m Q4 2023 Q4 2022 % Change
Net Sales 1,215 1,242 +8.5%
Other revenues 14 16 -12.5%
Gross profit 747 767 +9.0%
Gross margin % 61.5%1 61.8%1
R&D (56) (61) -4.9%
SG&A (473) (448) +12.9%
Operating Expenses (529) (509) +10.8%
Other current operating income & expenses 84 38
Business Operating Income 304 295 +22.7%
Sales growth
+8.5% due to Qunol
acquisition and continued
strong business performance
of Digestive Wellness
SG&A
+12.9% driven by increased
investment into advertising
and promotion of key brands
BOI margin
+1.2ppt due to the
acquisition of Qunol
R&D appendices

2024 currency sensitivity and Q4 2023 currency exposure
US $ 46.0%
Euro € 21.0%
Chinese Yuan 5.7%
Japanese Yen 3.7%
Brazilian Real 2.0%
Mexican pesos 2.7%
Canadian $ 1.6%
British Pound 1.2%
Australian $ 1.2%
South Korean won 1.1%
Others 13.8%
Currency exposure on Q4 2023 sales
2024 Business EPS currency sensitivity
Currency Variation Business EPS sensitivity
U.S. Dollar + 0.05 USD/EUR - EUR 0.17
Japanese Yen + 5 JPY/EUR - EUR 0.02
Chinese Yuan + 0.2 CNY/EUR - EUR 0.02
Brazilian Real + 0.4 BRL/EUR - EUR 0.01
Russian Ruble + 10 RUB/EUR - EUR 0.01
Currency average rates
Q4 2022 Q4 2023 % change
EUR/USD 1.021 1.076 +5.4%
EUR/JPY 144.203 159.030 +10.3%
EUR/CNY 7.264 7.778 +7.1%
EUR/BRL 5.372 5.329 -0.8%
EUR/RUB 64.072 99.644 +55.5%
R&D appendices

ESG
appendices
R&D appendices

Sanofi ESG FY achievements
Ambition Progress
FY 2023 FY 2022
Sanofi
Global Health
Reach 1.5 million NCD patients
by 2026 (cumulative since 2022)
and 2 million by 2030
261,977 patients treated in
31 countries
33 active healthcare partnerships in
15 countries
3 investment though the
Impact fund
185,151 patients treated
in 28 countries
19 active healthcare
partnerships in
11 countries
1 investment though
the Impact fund
Vials
donations
Donate 100,000 vials a year to
treat people with rare diseases,
via the Humanitarian Program
launched by Sanofi Specialty Care
124,136 vials donated
121,025 vials donated
Global
access plans
Develop a Global access plan
for all new products to make
them available within two years
after first launch
8 Global Access plans initiated
or developed covering more than
12 indications
2 Global Access
Plans initiated
Affordable access
Figures presented are YTD.
R&D appendices

Ambition Progress
FY 2023 FY 2022
Sleeping
sickness
Develop and supply innovative
treatments to support the
elimination of sleeping sickness
by 2030
Data updated annually, next update
in Q2 2024
1.5 million patients tested
837 patients treated
Polio Provide inactivated polio vaccines
(IPV) to UNICEF for GAVI countries
to support polio eradication efforts
35 million IPV doses supplied
to UNICEF for GAVI countries
47 million IPV doses
supplied to UNICEF for
GAVI countries
Pediatric cancer
treatment
development
Develop innovative treatments to
eliminate cancer death in children
3 assets undergoing
pre-clinical assessment
First pediatric patient dosed with
1 clinical asset (less than 2 years
after the 1st adult patient was
dosed with this compound)
1 asset pre-clinical
assessment complete
1 asset in protocol
preparation for clinical
study
1 additional asset
identified for clinical
development
R&D for unmet needs
R&D appendices

Ambition Progress
FY 2023 FY 2022
Climate change -
carbon footprint
CO2 emissions
55% reduction in scope 1&2
greenhouse gas emissions (CO2
equivalent) by 2030 (cumulative
vs 2019 baseline) to contribute to
carbon neutrality by 2030 and net
zero emissions by 2045 (all scopes)
38% GHG reduction
vs 2019
29% GHG reduction
vs 2019
Renewable
electricity
100% of renewable electricity
in all our sites by 2030
79% 62%
Eco-car
fleet
100% eco-car fleet in 2030 43% eco-car fleet 34% eco-car fleet
Blister free syringe
vaccines
100% blister free syringe
vaccines blister packs by 2027
39% blister free
syringe vaccines
33% blister free
syringe vaccines
Eco-design All new products to be
eco-designed by 2025
13 LCAs completed & 2 in progress
(new and marketed products)
7 LCAs completed &
1 in progress (new and
marketed products)
Eco design digital
solution launched
Planet Care
R&D appendices

Ambition Progress
FY 2023 FY 2022
Global Gender
balance
Ambition of 50% of women
in senior leadership roles by 2025
44% 42%
Ambition of 40% of women
in executive roles by 2025
40% 37%
Engagement with
communities
Engage socially and economically
with all communities where
we operate
12,240 volunteers
75,376 hours
6,825 volunteers
46,976 hours
From Leaders
to Citizens
100% of Sanofi leaders have
CSR in their development path
71% of the leaders have
completed the eLearning phase
30% of the leaders have
completed the full program
>50% of the leaders
have completed the
eLearning phase
In and beyond the workplace
R&D appendices

Scores assigned by the rating agencies are not equivalent.
Sanofi ESG ratings
Rating agencies
SCORE
87/100
21.2
Medium risk
79/100 A
Climate
Change: A
Water: A-
B 4.5/5 3.47/5 65/100
86/100 21.5 78/100 A A/A B 4.3/5 3.47/5 64/100
One of the highest
scores across all
sectors globally
81 points for its
solid fundamentals
& strong
preparedness
opinion of
6 points
19th
among 419
pharmaceutical
companies
Percentile of 99
within 348 scored
companies in the
industry
Score stable since
2021
Leading position 1st
decile of the
476 companies
in the industry
With very high
rating across the
3 pillars ESG
Top 10
company
1st
pharmaceutical
company out of 57
Score improving
since 2018
vs. previous rating
R&D appendices

Abbreviations
AA Alopecia Areata
AAT Alpha-1-Antitrypsin
AATD Alpha-1-Antitrypsin Deficiency
AAV Adeno-Associated Virus
Ab Antibody
AD Atopic Dermatitis
ADC Antibody Drug Conjugate
ALS Amyotrophic Lateral Sclerosis
BCMA B-Cell Maturation Antigen
BP Bullous Pemphigoid
BTK Bruton’s Tyrosine Kinase
CD Cluster of Differentiation
CEACAM5 Carcinoembryonic Antigen Cell Adhesion Molecule 5
CIDP Chronic Inflammatory Demyelinating
Polyneuropathy
COPD Chronic Obstructive Pulmonary Disease
CPUO Chronic Pruritus of Unknown Origin
CRC Colerectal Cancer
CRSwNP Chronic Rhinosinusitis with Nasal Polyps
CSR Corporate Social Responsibility
CSU Chronic Spontaneous Urticaria
ERT Enzyme Replacement Therapy
ExPEC Extraintestinal pathogenic E. coli
FGFR3 Fibroblast Growth Factor Receptor 3
GAA Acid Alpha-Glucosidase
GCS Glucosylceramide Synthase
GHG Greenhouse Gas
GPC3 Glypican-3
HD High Dose
HS Hidradenitis Suppurativa
HER2 Human Epidermal growth factor Receptor 2
hMPV human Metapneumovirus
IA Interim analysis
IBD Inflammatory Bowel Disease
IGF1R Insulin Like Growth Factor 1 Receptor
IIV Inactivated Influenza Vaccine
IL Interleukin
ILT2 Ig-like transcript 2
IPV Inactivated Poliomyelitis Vaccine
IRAK4 Interleukin 1 Receptor Associated Kinase 4
ITP Immune Thrombocytopenia
IVIg Intravenous Immunoglobulin
LCA Life Cycle Assessment
LOE Loss Of Exclusivity
mAb monoclonal Antibody
MM Multiple Myeloma
mRNA messenger RNA
MS Multiple Sclerosis
NCD Non-Communicable Diseases
NK Natural Killer
PAH Phenylalanine Hydroxylase
PCV Pneumococcal Conjugated Vaccine
PD1 Programmed Death protein 1
PN Prurigo Nodularis
PPMS Primary Progressive Multiple Sclerosis
PPH Polio, Pertussis, Haemophilus influenzae b (Hib)
QIV Quadrivalent Influenza Vaccine
RIPK1 Receptor-Interacting serine/threonine-Protein
Kinase 1
RA Rheumatoid Arthritis
RMS Relapsing Multiple Sclerosis
RNAi RNA interference
RRMM Relapsed-Refractory Multiple Myeloma
RSV Respiratory Syncytial Virus
SjS Sjogren's Syndrome
SLE Systemic Lupus Erythematosus
SOC Standard of care
SPMS Secondary-Progressive Multiple Sclerosis
SSc Systemic Sclerosis
TCR T Cell Receptor
Te Transplant eligible
TGFb Transforming Growth Factor beta
Ti Transplant ineligible
TL1A TNF-like Ligand 1A
TNF Tumor Necrosis Factor
TSLP Thymic Stromal Lymphopoietin
T1D Type 1 Diabetes
UC Ulcerative Colitis
VBP Volume-based Procurement
wAIHA Warn Autoimmune Hemolytic Anemia
R&D appendices

Collaborations
Ref Name Developed in collaboration with…
A Dupixent
itepekimab
Kevzara
Regeneron
B frexalimab ImmuNext
C ExPEC9V Vaccine Janssen Pharmaceuticals, Inc., a Johnson & Johnson company
D eclitasertib
SAR443820
Denali
E SAR444656 Kymera
F SAR447189 Teva Pharmaceuticals
G SP0202 SK
H SAR446159 ABL Bio
I SAR444836 Medicinova
J SAR444881 Biond Biologics
K SAR443579
SAR445514
Innate Pharma
L SAR445953 Seagen
R&D appendices

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