Cellectis Receives $20 Million Convertible Note Under Collaboration Agreement with its Partner Cytovia Therapeutics

On April 27, 2022 Cellectis (the "Company") (Euronext Growth: ALCLS – NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies, reported that its partner Cytovia Therapeutics, LLC ("Cytovia"), a biopharmaceutical company empowering natural killer ("NK") cells to fight cancer through stem cell engineering and multispecific antibodies, entered into a definitive business combination agreement with Isleworth Healthcare Acquisition Corp. (NASDAQ: ISLE) ("Isleworth"), a Special Purpose Acquisition Company ("SPAC") (Press release, Cellectis, APR 27, 2022, View Source [SID1234613010]).

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Concurrent with the business combination agreement, Cellectis received a $20 million convertible note in payment of the upfront collaboration consideration provided for pursuant to the research collaboration and non-exclusive license agreement entered between Cellectis and Cytovia in February 2021. The terms of the note provide for conversion into common stock of the combined company upon completion of the business combination, which is subject to the satisfaction or waiver of customary closing conditions. In connection with this convertible note, Cellectis received a warrant to purchase additional shares of the combined company representing up to 35% of the shares issued upon conversion of the note at a predetermined exercise price, with the number of shares issuable upon exercise and the exercise subject to certain adjustments.

« We are impressed by the progress Cytovia has accomplished in the past months. Cytovia shares Cellectis’ mission to provide life-saving off-the-shelf allogeneic cell therapies to patients, and we are excited to be providing them with best-in-class TALEN gene editing for cell therapy applications. Congratulations to the Cytovia team for this transaction, which is an important milestone as they continue their journey to progress gene-edited NK therapeutics towards a cure for cancer! » said André Choulika, CEO of Cellectis.

Cellectis and Cytovia’s research and development collaboration:

In February 2021, Cellectis and Cytovia entered into a strategic research and development collaboration to develop TALEN gene-edited iPSC NK and CAR-NK cells. In November 2021, Cellectis and Cytovia extended their collaboration to include new CAR target and development in China by Cytovia’s strategic partner, CytoLynx Therapeutics.

Financial terms of the collaboration include the $20 million convertible note as well as up to $805 million of development, regulatory, and sales milestones and single-digit royalty payments on the net sales of all partnered products commercialized by Cytovia.

Cellectis is developing custom TALEN, which Cytovia uses to edit iPSCs. Cytovia is responsible for the differentiation and expansion of the gene-edited iPSC master cell bank into NK cells and is conducting the pre-clinical evaluation, clinical development, and commercialization of the mutually-agreed-upon selected therapeutic candidates. Cellectis has granted Cytovia a worldwide license under the patent rights over which Cellectis has control in this field, including in China, in order for Cytovia to modify NK cells to address multiple gene-targets for therapeutic use in several cancer indications.

HiFiBiO Therapeutics to Present Trial in Progress Poster for HFB200301 at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting

On April 27, 2022 HiFiBiO Therapeutics, a multinational clinical-stage biotherapeutics company, reported that clinical trial investigator, Alexander I Spira, MD, PhD, FACP, Co-Director of the Virginia Cancer Specialists (VCS) Research Institute and Director of the Thoracic and Phase I Program, will present a Trials in Progress Poster for HFB200301 on Sunday, June 5 from 8:00 AM to 11:00 AM CT at the 2022 ASCO (Free ASCO Whitepaper) Annual Meeting held June 3 – 7, 2022, in Chicago, IL (Press release, HiFiBiO Therapeutics, APR 27, 2022, View Source [SID1234613029]).

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"HFB200301 is an anti-TNFR2 antibody that induces T cell and natural killer cell activation, demonstrated in preclinical models. The unique mechanism of action indicates that HFB200301 functions as a bridge between innate and adaptive immunity" said Dr. Alexander Spira. "We are excited to have VCS medical staff and patients to be a part of this Phase I clinical study (NCT05238883). Our hospital’s clinical strength combined with HiFiBiO’s innovative DIS approach will hopefully accelerate the clinical development of HFB200301 for cancer patients."

"We look forward to sharing the clinical study for HFB200301, a first-in-class cancer therapeutic targeting TNFR2 as well as our DIS indications selection strategy," said Luigi Manenti, MD, Chief Medical Officer of HiFiBiO Therapeutics. "With strong in-vivo efficacy as a monotherapy and in combination with anti-PD-1 in preclinical models, we believe it has significant potential in DIS selected tumor types including EBV+ gastric cancer, PD-L1+ pleural mesothelioma and clear cell renal cell carcinoma."

Details on the poster presentation are as follows:

Title: Phase I study of HFB200301, a first-in-class TNFR2 agonist monoclonal antibody in patients with solid tumors selected via Drug Intelligent Science (DIS)
Abstract Number: TPS2670
Poster Session: Developmental Therapeutics – Immunotherapy
Session Date and Time: Poster Session 3 – Sunday, June 5 at 8:00 AM – 11:00 AM CT

The abstract will be available through the ASCO (Free ASCO Whitepaper) Meeting Library at View Source on May 26, 2022.

HFB200301 (TNFR2)
HFB200301 is a first-in-class agonistic anti-TNFR2 antibody that binds potently and selectively to TNFR2 and induces the activation of CD4 T cells, CD8 T cells and NK cells. In vivo, HFB200301 demonstrates potent antitumor activity as a single agent and in combination with anti-PD-1. HiFiBiO is applying a biomarker strategy by leveraging its DIS platform to select indications who may benefit the most from HFB200301 treatment.

ASLAN Pharmaceuticals Reports First Quarter 2022 Financial Results and Provides Corporate Update

On April 27, 2022 ASLAN Pharmaceuticals (Nasdaq: ASLN), a clinical-stage, immunology-focused biopharmaceutical company developing innovative treatments to transform the lives of patients, reported financial results for the first quarter ended March 31, 2022, and provided an update on recent corporate activities (Press release, ASLAN Pharmaceuticals, APR 27, 2022, View Source [SID1234613045]).

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"We have made strong progress in the first quarter of the year with the initiation of TREK-AD, the global Phase 2b trial of eblasakimab, a potential first-in-class antibody targeting the IL-13 receptor, and welcoming new team members to support the late-stage development of eblasakimab," said Dr Carl Firth, CEO, ASLAN Pharmaceuticals. "Following the presentation of the positive data from our proof-of-concept study in the late-breaker session at the American Academy of Dermatology meeting, we plan to publish new data from this study in the coming months to support the potential of eblasakimab as a differentiated therapy for patients with moderate-to-severe AD. By targeting the receptor, and blocking signaling of both IL-13 and IL-4 through the Type 2 receptor, eblasakimab may be effective in a range of other Type 2-driven comorbidities, which is very important in this patient population."

First quarter 2022 and recent business highlights

Q1 and recent clinical developments

In January, the TREK-AD (TRials with EblasaKimab in Atopic Dermatitis) Phase 2b trial was initiated to evaluate the efficacy and safety of eblasakimab in patients with moderate-to-severe AD. The randomized, double-blind, placebo-controlled, multi-center, dose-ranging clinical trial is evaluating five treatment arms (four active treatment arms and one placebo arm) and is expected to enroll approximately 300 patients across sites in North America, Europe and Asia Pacific. Topline data from the study is expected in the first half of 2023.
In January, results of an interim analysis of the completed Phase 1b proof-of-concept study of eblasakimab in AD were accepted for poster presentation at the 2022 Winter Clinical Dermatology Conference – Hawaii.
In January, the Company hosted the second episode in its series of Key Opinion Leader (KOL) webinars, the "A4 (Aspects of Atopic Dermatitis and ASLAN004) Series: Dialogues with International Thought Leaders in Dermatology". Dr April Armstrong, MD MPH, discussed the key clinical study parameters likely to impact patient responses and clinical trial outcomes in AD. Replay for the webinar is available here. The replays can also be found on the "Events and Presentations" section in ASLAN’s Investor Relations website.
In March, key efficacy and safety data from the completed Phase 1b proof-of-concept study that demonstrated eblasakimab’s potential to offer a differentiated treatment option for patients were presented in a late-breaker oral session at the 2022 American Academy of Dermatology Annual Meeting. These data confirmed that eblasakimab’s inhibition of the IL-13 receptor, blocking signaling of both IL-13 and IL-4 through the Type 2 receptor, can contribute significantly to reducing inflammation in AD. ASLAN believes that this ‘dual blockade’ may not only offer a differentiated treatment option for patients in terms of safety and dosing regimen, but may also address other allergic comorbidities that many of these patients suffer from.
Corporate updates

In March, Alex Kaoukhov, MD, was appointed as Chief Medical Officer based in the Company’s U.S. office. Alex has more than 20 years of global drug development experience in the U.S. and Europe, and was most recently Head of Clinical Development, Senior Vice President at Bioniz Therapeutics, where he established and managed a team responsible for the development of therapeutic assets for the treatment of skin and gastrointestinal autoimmune diseases. Prior to this, Alex served as Head of Global Development at Almirall, where he oversaw global clinical and non-clinical development programs. He also was responsible for business development activities including the in-licensing of lebrikizumab for Europe. Prior to Almirall, Alex was Associate Vice President of Clinical Development at Allergan and served in clinical development leadership roles at Novartis and Galderma.
Anticipated upcoming milestones

Initiation of Phase 2 study of farudodstat, also known as ASLAN003, in inflammatory bowel disease is planned for the first half of 2022.
New data on biomarkers and patient reported outcome measures from the Phase 1b proof-of-concept study of eblasakimab expected in the second half of 2022.
Topline data from the Phase 2b TREK-AD study of eblasakimab is expected in the first half of 2023.
First quarter 2022 financial highlights

As of March 31, 2022, the Company had cash, cash equivalents and short-term investments of $87.4 million.
Cash used in operations for the first quarter of 2022 was US$7.2 million compared to US$7.6 million in the same period in 2021.
Research and development expenses were US$9.4 million in the first quarter of 2022 compared to US$3.8 million in the first quarter of 2021. The increase was driven by clinical development expenses and manufacturing costs related to eblasakimab and the TREK-AD Phase 2b trial.
General and administrative expenses were US$2.5 million in the first quarter of 2022 compared to US$3.1 million in the first quarter of 2021. The decrease was due to financing costs incurred in the first quarter of 2021.
Net loss attributable to stockholders for the first quarter of 2022 was US$12.9 million or $0.19 per ADS compared to a net loss of US$6.7 million or $0.13 per ADS for the first quarter of 2021.
The weighted average number of American Depositary Shares (ADSs) outstanding in the computation of basic loss per share for the first quarter of 2022 was 69.7 million (representing 348.7 million ordinary shares) compared to 51.4 million (representing 257.2 million ordinary shares) for the first quarter of 2021. One ADS is the equivalent of five ordinary shares.

Aldeyra Therapeutics Schedules Webcast and Conference Call to Report First-Quarter 2022 Financial Results and Discuss Recent Corporate Highlights

On April 27, 2022 Aldeyra Therapeutics, Inc. (Nasdaq: ALDX) (Aldeyra) reported that it will host a conference call at 8:00 a.m. ET Thursday, May 5, 2022 to report financial results for the quarter ended March 31, 2022 and discuss recent corporate highlights (Press release, Aldeyra Therapeutics, APR 27, 2022, View Source [SID1234613062]).

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The dial-in numbers are (844) 200-6205 for domestic callers and (929) 526-1599 for international callers. The access code is 742862. A live audio webcast of the conference call also will be accessible from the "Investors & Media" section of Aldeyra’s website at View Source

After the live webcast, the event will remain archived on Aldeyra’s website for 90 days.

Ipsen delivers a strong sales performance in the first quarter of 2022

On April 2022 – Ipsen (Euronext: IPN; ADR: IPSEY), a global specialty-driven biopharmaceutical group, reported its sales performance for the first quarter of 2022 (Presentation, Ipsen, APR 27, 2022, View Source [SID1234613078]).
Highlights
− A strong first-quarter total-sales performance, with growth of 9.6% at CER1
(12.5% as reported) to
€687.9m, driven by Decapeptyl (triptorelin), Dysport (botulinum toxin type A), Cabometyx
(cabozantinib) and Onivyde (irinotecan liposome injection) double-digit growth and flat sales of
Somatuline (lanreotide)
− Confirmation of full-year guidance for 2022, with total-sales growth greater than 2.0% at CER1 and a core
operating margin greater than 35.0% of total sales
− Transaction announced in February 2022 for the divestment of the Consumer HealthCare (CHC) business
anticipated to be completed by end of Q3 2022
Q1 2022 total sales
Total sales in this announcement are unaudited IFRS consolidated sales and reflect Specialty Care sales only,
in accordance with IFRS 5.
First Quarter
2022 2021 % change
€m €m Actual CER1
Oncology 556.4 495.4 12.3% 8.9%
Neuroscience 120.2 103.1 16.6% 15.7%
Rare Disease 11.3 13.1 -13.4% -15.0%
Total 687.9 611.5 12.5% 9.6%
David Loew, Chief Executive Officer, commented:
"The execution of our strategy was reflected in our first-quarter performance across the business. The strong
sales were in line with our expectations, with Decapeptyl, Dysport, Cabometyx and Onivyde all delivering
double-digit growth. Our guidance for the year, which assumes increasing levels of competition for Somatuline,
is underpinned by our strong platform of growth across these core and innovative medicines.
Alongside the anticipated U.S. regulatory resubmission for palovarotene in the first half of the year, we look
forward to a number of important data readouts in the second half, while our pipeline will continue to be
replenished through the external-innovation strategy. It is an exciting time for Ipsen as we deliver on our
strategy, produce strong results, expand our pipeline and focus together, for patients and society."
1 At constant exchange rates (CER), which exclude any foreign-exchange impact by recalculating the performance for the relevant period
by applying the exchange rates used for the prior period.
2
Full-year 2022 guidance
Ipsen today confirms its financial guidance for FY 2022, which excludes any contribution from CHC:
− Total-sales growth greater than 2.0%, at CER2
. Based on the level of exchange rates in Q1 2022, Ipsen
anticipates an additional favorable impact of 2% from currencies in the year
− Core operating margin greater than 35.0% of total sales, excluding any potential impact of incremental
investments from future external-innovation transactions
This guidance incorporates expectations for Somatuline of further launches of generic lanreotide in other
countries in the E.U., as well as increased competition in the U.S.
Ongoing conflict in Ukraine
Ipsen is firmly committed to the safety and care of its employees and to providing essential support and access
to its treatments and medicines for patients.
Since the beginning of the conflict in Ukraine, Ipsen’s immediate actions have been to ensure that all
colleagues are safe and to limit any impact on the supply of medicines. The Company has also provided
humanitarian relief via a donation of €1.5m in favor of two highly reputed humanitarian organizations: Tulipe,
a pharmaceutical distributor managing donations from health companies to meet the emergency needs of
populations in distress, and The Red Cross.
Ipsen’s position is to continue to serve patients with their healthcare needs, regardless of their country origin
and in compliance with applicable laws. In Russia, the Company has, however, suspended several promotional
activities, including advertising. No new clinical trials will be initiated in Russia.
In 2021, Ipsen’s Specialty Care sales in Russia and Ukraine were less than 3.0% of total Specialty Care sales.
Consumer HealthCare
In February 2022, Ipsen announced that it had entered into exclusive negotiations with Mayoly Spindler for the
divestment of its global CHC business, a major step forward in the Company’s execution of its strategic
roadmap towards building a more-focused Ipsen, centering on Specialty Care. Ipsen confirms that the
transaction is anticipated to close by the end of Q3 2022, subject to regulatory approvals and customary closing
conditions.
Conference call
A conference call and webcast for investors and analysts will begin at 2pm Paris time today. Participants should
dial in to the call early and can register here; a recording will be available on ipsen.com, while the webcast can
be accessed here. The event ID is 9681287.
Calendar
The Company intends to publish its H1 2022 results on 28 July 2022.
Notes
All financial figures are in € millions (€m). The performance shown in this announcement covers the threemonth period to 31 March 2022 (the quarter or Q1 2022), compared to the three-month period to 31 March
2021 (Q1 2021).
2 At CER, which excludes any foreign-exchange impact by recalculating the performance for the relevant period by applying the exchange
rates used for the prior period.
3
Ipsen
Ipsen is a global, mid-sized biopharmaceutical company focused on transformative medicines in Oncology,
Rare Disease and Neuroscience. With Specialty Care sales of €2.6bn in FY 2021, Ipsen sells medicines in
over 100 countries. Alongside its external-innovation strategy, the Company’s research and development
efforts are focused on its innovative and differentiated technological platforms located in the heart of leading
biotechnological and life-science hubs: Paris-Saclay, France; Oxford, U.K.; Cambridge, U.S.; Shanghai, China.
Ipsen, excluding its Consumer HealthCare business, has around 4,500 colleagues worldwide and is listed in
Paris (Euronext: IPN) and in the U.S. through a Sponsored Level I American Depositary Receipt program
(ADR: IPSEY). For more information, visit ipsen.com.
Contacts
Investors
Craig Marks
Vice President, Investor Relations
+44 (0)7584 349 193
Adrien Dupin de Saint-Cyr
Investor Relations Manager
+33 6 64 26 17 49
Media
Mai Tran
Global Communications Director
+ 33 6 64 74 70 80
Ioana Piscociu
Senior Manager, Global Media Relations
+33 6 69 09 12 96
4
Sales by therapeutic area and medicine
Total sales in this announcement are unaudited IFRS consolidated sales and reflect Specialty Care sales only,
in accordance with IFRS 5.
A breakdown of medicine sales by geographical area is shown in the appendix.
First Quarter
2022 2021 % change
€m €m Actual CER3
Oncology 556.4 495.4 12.3% 8.9%
Somatuline 286.0 277.0 3.3% -0.7%
Decapeptyl 129.2 106.3 21.6% 19.0%
Cabometyx 98.9 83.3 18.8% 18.5%
Onivyde 40.1 26.5 51.4% 40.9%
Other Oncology 2.2 2.4 -8.5% -9.2%
Neuroscience 120.2 103.1 16.6% 15.7%
Dysport 118.4 101.8 16.3% 15.2%
Other Neuroscience 1.7 1.3 34.4% 49.8%
Rare Disease 11.3 13.1 -13.4% -15.0%
NutropinAq 7.1 8.5 -15.8% -16.1%
Increlex 4.2 4.6 -9.0% -13.0%
Total Sales 687.9 611.5 12.5% 9.6%
Oncology
Oncology sales of €556.4m represented growth of 8.9%3 and comprised 80.9% of total sales in the quarter
(Q1 2021: 81.0%).
a) Somatuline sales declined by 0.7%3
to €286.0m. In North America, sales fell by 6.9%3
, with
encouraging volume growth supported by continued market-share gains more than offset by adverse
pricing, primarily a result of unfavorable movements in channel mix, as well as changes in wholesalerbuying patterns. In Europe, effects from the launch of generic lanreotide in some European markets
reduced sales growth to 0.4%3
, while sales in the Rest of the World grew by 39.3%3
.
b) Decapeptyl sales of €129.2m represented growth of 19.0%3
, mainly driven by market growth and
inventory in China, along with continued market-share gains in Europe, primarily in France and Italy.
c) Cabometyx sales reached €98.9m, up by 18.5%3
, driven by a strong volume uptake across most
geographies, mainly in the renal cell carcinoma indication.
d) Onivyde sales of €40.1m, growing by 40.9%3
, were primarily driven by sales to Ipsen’s ex-U.S.
partner, as well as market-share gains and volume growth in the U.S.
3 At CER, which excludes any foreign-exchange impact by recalculating the performance for the relevant period by applying the exchange
rates used for the prior period.
5
Neuroscience
Neuroscience sales increased by 15.7%4
to €120.2m and comprised 17.5% of total sales in the quarter
(Q1 2021: 16.9%).
Dysport sales reached €118.4m, up by 15.2%4
, driven by a continued strong performance in most aesthetics
markets, including those operated by Ipsen’s partner, Galderma, as well as therapeutics markets in Europe,
North America and the Middle East.
Rare Disease
Rare Disease sales declined by 15.0%4
to €11.3m and comprised 1.6% of total sales in the quarter (Q1 2021:
2.1%).
NutropinAq (somatropin) sales of €7.1m, a decline of 16.1%4
, reflected competitive pressures across Europe.
Increlex (mecasermin) sales of €4.2m, a decrease of 13.0%4
, were impacted by lower demand in the U.S.
Sales by geographical area
A breakdown of medicine sales by geographical area is shown in the appendix.
First Quarter
2022 2021 % change
€m €m Actual CER4
North America 226.4 207.0 9.4% 1.8%
Europe5 304.7 288.8 5.5% 4.8%
Rest of the World 156.9 115.7 35.5% 35.4%
Total Sales 687.9 611.5 12.5% 9.6%
North America
Sales of €226.4m in the quarter reflected growth of 1.8%4
, driven by strong performances from Dysport and
Onivyde, offset by the Somatuline sales decline of 6.9%4
.
North America sales comprised 32.9% of total sales in the quarter (Q1 2021: 33.8%).
Europe
Sales reached €304.7m in the quarter, an increase of 4.8%4
, mainly driven by Decapeptyl’s market-share
uptakes in major countries and Cabometyx, with solid performances in both France and Spain. Effects from
the launch of generic lanreotide in some European markets reduced Somatuline sales growth to 0.4%4
, while
Dysport sales were impacted by shipment phasing to Ipsen’s partner, Galderma.
Sales in Europe comprised 44.3% of total sales in the quarter (Q1 2021: 47.2%).
4 At CER, which excludes any foreign-exchange impact by recalculating the performance for the relevant period by applying the exchange
rates used for the prior period.
5
In this announcement, Europe is defined as the E.U., the U.K., Iceland, Liechtenstein, Norway and Switzerland.
6
Rest of the World
Sales reached €156.9m in the quarter, an increase of 35.4%6
, driven by solid volumes growth in Oncology and
Neuroscience. Decapeptyl sales increased by 31.6%6
, reflecting volume uptakes in Asia, partly reflecting
inventory increases in China, while Cabometyx and Somatuline delivered further market-share gains across
several countries. Dysport sales were primarily driven by solid performances in aesthetics markets across all
geographies, as well as continued growth in therapeutics markets.
Rest of the World sales comprised 22.8% of total sales in the quarter (Q1 2021: 18.9%).
Consumer HealthCare
CHC sales of €54.7m, an increase of 14.8%6
, were driven by the growth of Smecta (diosmectite), reflecting
the COVID-19 recovery and the performance in Europe, China and Vietnam.
Total sales in this announcement exclude CHC sales, in accordance with IFRS 5.
6 At CER, which excludes any foreign-exchange impact by recalculating the performance for the relevant period by applying the exchange
rates used for the prior period.
7
Forward-looking statements
The forward-looking statements, objectives and targets contained herein are based on Ipsen’s management
strategy, current views and assumptions. Such statements involve known and unknown risks and uncertainties
that may cause actual results, performance or events to differ materially from those anticipated herein. All of
the above risks could affect Ipsen’s future ability to achieve its financial targets, which were set assuming
reasonable macroeconomic conditions based on the information available today. Use of the words ‘believes’,
‘anticipates’ and ‘expects’ and similar expressions are intended to identify forward-looking statements,
including Ipsen’s expectations regarding future events, including regulatory filings and determinations.
Moreover, the targets described in this document were prepared without taking into account external growth
assumptions and potential future acquisitions, which may alter these parameters. These objectives are based
on data and assumptions regarded as reasonable by Ipsen. These targets depend on conditions or facts likely
to happen in the future, and not exclusively on historical data. Actual results may depart significantly from these
targets given the occurrence of certain risks and uncertainties, notably the fact that a promising medicine in
early development phase or clinical trial may end up never being launched on the market or reaching its
commercial targets, notably for regulatory or competition reasons. Ipsen must face or might face competition
from generic medicine that might translate into a loss of market share. Furthermore, the research and
development process involves several stages each of which involves the substantial risk that Ipsen may fail to
achieve its objectives and be forced to abandon its efforts with regards to a medicine in which it has invested
significant sums. Therefore, Ipsen cannot be certain that favorable results obtained during preclinical trials will
be confirmed subsequently during clinical trials, or that the results of clinical trials will be sufficient to
demonstrate the safe and effective nature of the medicine concerned. There can be no guarantees a medicine
will receive the necessary regulatory approvals or that the medicine will prove to be commercially successful.
If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ
materially from those set forth in the forward-looking statements. Other risks and uncertainties include but are
not limited to, general industry conditions and competition; general economic factors, including interest rate
and currency exchange rate fluctuations; the impact of pharmaceutical industry regulation and healthcare
legislation; global trends toward healthcare cost containment; technological advances, new medicine and
patents attained by competitors; challenges inherent in new-medicine development, including obtaining
regulatory approval; Ipsen’s ability to accurately predict future market conditions; manufacturing difficulties or
delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of
Ipsen’s patents and other protections for innovative medicines; and the exposure to litigation, including patent
litigation, and/or regulatory actions. Ipsen also depends on third parties to develop and market some of its
medicines which could potentially generate substantial royalties; these partners could behave in such ways
which could cause damage to Ipsen’s activities and financial results. Ipsen cannot be certain that its partners
will fulfil their obligations. It might be unable to obtain any benefit from those agreements. A default by any of
Ipsen’s partners could generate lower revenues than expected. Such situations could have a negative impact
on Ipsen’s business, financial position or performance. Ipsen expressly disclaims any obligation or undertaking
to update or revise any forward-looking statements, targets or estimates contained in this press release to
reflect any change in events, conditions, assumptions or circumstances on which any such statements are
based, unless so required by applicable law. Ipsen’s business is subject to the risk factors outlined in its
registration documents filed with the French Autorité des Marchés Financiers. The risks and uncertainties set
out are not exhaustive and the reader is advised to refer to Ipsen’s 2021 Universal Registration Document,
available on ipsen.com.
8
Appendix: geographic breakdown of total sales by medicine
First Quarter
Total North America Europe7 Rest of the World
2022 2021 % change 2022 2021 % change 2022 2021 % change 2022 2021 % change
€m €m Actual CER8 €m €m Actual CER8 €m €m Actual CER8 €m €m Actual CER8
Oncology 556.4 495.4 12.3% 8.9% 184.3 176.2 4.6% -2.7% 267.9 247.1 8.4% 7.6% 104.3 72.1 44.6% 42.1%
Somatuline 286.0 277.0 3.3% -0.7% 151.5 151.5 0.0% -6.9% 105.5 104.4 1.1% 0.4% 29.0 21.1 37.3% 39.3%
Decapeptyl 129.2 106.3 21.6% 19.0% – – – – 73.7 66.0 11.7% 11.3% 55.5 40.3 37.9% 31.6%
Cabometyx 98.9 83.3 18.8% 18.5% 4.0 3.3 19.0% 10.7% 75.2 69.2 8.8% 8.3% 19.7 10.8 82.7% 85.9%
Onivyde 40.1 26.5 51.4% 40.9% 28.7 21.2 35.0% 25.6% 11.4 5.3 117.4% 103.0% – – – –
Other Oncology 2.2 2.4 -8.5% -9.2% 0.1 0.2 -39.7% -43.9% 2.0 2.3 -12.6% -12.9% 0.1 0.0 n.a. n.a.
Neuroscience 120.2 103.1 16.6% 15.7% 39.5 27.9 41.7% 32.5% 28.4 31.9 -11.0% -11.5% 52.3 43.3 20.8% 24.5%
Dysport 118.4 101.8 16.3% 15.2% 39.5 27.9 41.7% 32.5% 28.4 31.9 -11.0% -11.5% 50.5 42.0 20.4% 23.7%
Other Neuroscience 1.7 1.3 34.4% 49.8% – – – – – – – – 1.7 1.3 34.4% 49.8%
Rare Disease 11.3 13.1 -13.4% -15.0% 2.6 2.9 -10.1% -16.4% 8.4 9.8 -14.5% -14.7% 0.3 0.3 -11.4% -11.4%
NutropinAq 7.1 8.5 -15.8% -16.1% – – – – 6.8 8.2 -16.5% -16.8% 0.3 0.3 7.6% 7.2%
Increlex 4.2 4.6 -9.0% -13.0% 2.6 2.9 -10.1% -16.4% 1.5 1.6 -3.8% -4.0% 0.0 0.1 -67.1% -67.3%
Total Sales 687.9 611.5 12.5% 9.6% 226.4 207.0 9.4% 1.8% 304.7 288.8 5.5% 4.8% 156.9 115.7 35.5% 35.4%
7
In this announcement, Europe is defined as the E.U., the U.K., Iceland, Liechtenstein, Norway and Switzerland.
8 At CER, which excludes any foreign-exchange impact by recalculating the performance for the relevant period by applying the exchange rates used for the prior period.

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