Shield Therapeutics plc
("Shield"
or the "Company" or the "Group")
Unaudited Q2 2024 Trading
Update
ACCRUFeR® US Net Revenues
of $6.9m following 26% Increase in Q2
Prescriptions
23% sequential increase in
average net selling price to
$171/prescription
Increased balance sheet and
operational flexibility with $8.1 million cash on hand
plus $5.7 million from the China milestone monetization announced
post period end
London, UK, July 24 2024: Shield Therapeutics plc (LSE: STX), a commercial stage
pharmaceutical company that delivers ACCRUFeR®/Feraccru® (ferric
maltol), an innovative and differentiated specialty pharmaceutical
product, to address a significant unmet need for patients suffering
from iron deficiency (with or without anaemia) today
announced a Q2 2024 trading update highlighting a
strong recovery in U.S. ACCRUFeR® growth.
Shield delivered stand-out
sequential ACCRUFeR® revenue growth results of 69% in Q2 2024,
driven by robust increases in prescriptions, up 26% along with a
23% increase in average net selling price per prescription. This
has resulted in total H1 2024 ACCRUFeR® revenues of $11 million
(unaudited) and total prescriptions to 65,200, which represent
significant increases of ~250% and ~160% respectively compared to
H1 2023.
Snapshot of Positive Q2 2024 ACCURUFeR® Key Performance
Indicators (KPIs)
·
Total Net
Sales: $6.9 million, an increase of
69% vs. Q1 24 and 259% vs. Q2 23
·
Total
Prescriptions: -Over 36,400, an increase of 26% vs. Q1 24 and 145% vs. Q2
23
·
Average net selling price
per prescription: $171 vs. $139 in Q1 2024 and
$118 in Q2 2023
·
Cash and cash
equivalents: $8.1 million as of 30 June 2024
excluding the $5.7 million funding from the China milestone
monetization announced on July 3, 2024
Shield's new Interim Chief Executive Officer Anders Lundstrom
commented: "I am excited about stepping in as the
interim CEO and continue to build on the strong performance we
delivered in the 2nd quarter of 2024. Large states such
as California, NY, and Florida continue to drive a significant
portion of the increase in prescriptions, while Texas begins to
rebound. Our efforts on the operational side also showed
outstanding progress, with an increase in our net selling price of
23% which is a direct result of strategies and investments over the
past few quarters."
Mr. Lundstrom
continued "As we reflect on the first
full year of the Shield/Viatris launch of our expanded field force,
we are pleased that the market has responded in such a positive way
to our efforts to increase physician awareness and adoption of
ACCRUFeR®. This fortifies our continued belief the market potential
of ACCRUFeR® is significant. We are committed to delivering further
ACCRUFeR® growth making it the oral iron of choice for patients
with iron deficiency, with or without anemia."
The
information contained within this announcement is deemed by the
Company to constitute inside information as stipulated under the
Market Abuse Regulation (EU) No. 596/2014 (as it forms part of
domestic law by virtue of the European Union (Withdrawal) Act
2018). Upon the publication of this announcement via the Regulatory
Information Service, this inside information is now considered to
be in the public domain.
For further
information please contact:
Shield Therapeutics plc
|
www.shieldtherapeutics.com
|
Anders Lundstrom
Santosh Shanbhag, CFO
|
+44 (0)
191 511 8500
|
Nominated Adviser and Joint Broker
|
|
Peel Hunt LLP
|
|
James Steel/Patrick
Birkholm
|
+44 (0)20
7418 8900
|
|
|
Joint Broker
Cavendish Ltd
Geoff Nash/ George Dollemore/Nigel
Birks/Harriet
Ward
|
+44 (0)20
7220 0500
|
|
|
Financial PR & IR Advisor
|
|
Walbrook PR
|
|
Charlotte Edgar / Alice
Woodings
|
+44 (0)20
7933 8780 or shield@walbrookpr.com
|
|
|
Investor Contact (US Advisor)
LifeSci Advisors, LLC
Joyce Allaire
|
jallaire@lifesciadvisors.com
|
About Iron Deficiency and
Accrufer®/Feraccru®
Clinically low iron levels (aka iron
deficiency, ID) can cause serious health problems for adults of all
ages, across multiple therapeutic areas. Together, ID and ID with
anemia (IDA) affect about 20 million people in the US and represent
a $2.3B market opportunity. As the first and only FDA approved oral
iron to treat ID/IDA, Accrufer® has the potential to meet an
important unmet medical need for both physicians and
patients.
Accrufer®/Feraccru® (ferric maltol)
is a novel, stable, non-salt-based oral therapy for adults with
ID/IDA. The drug has a novel mechanism of absorption compared to other oral
iron therapies and has been shown to be an efficacious and
well-tolerated therapy in a range of clinical trials. More
information about Accrufer®/Feraccru®, including the product
label, can be found at: www.accrufer.com and www.feraccru.com.
About Shield Therapeutics plc
Shield is a commercial stage
specialty pharmaceutical company that delivers Accrufer®/Feraccru®
(ferric maltol), an innovative and differentiated pharmaceutical
product, to address a significant unmet need for patients suffering
from iron deficiency, with or without anemia. The Company has launched Accrufer® in the U.S. with an
exclusive, multi-year collaboration agreement with Viatris. Outside
of the U.S., the Company has licensed the rights to four specialty
pharmaceutical companies. Feraccru® is commercialized in the UK and
European Union by Norgine B.V., which also has marketing rights in
Australia and New Zealand. Shield also has an exclusive license
agreement with Beijing Aosaikang Pharmaceutical Co., Ltd., for the
development and commercialization of Accrufer®/ Feraccru® in China,
Hong Kong, Macau and Taiwan, with Korea Pharma Co., Ltd. for the
Republic of Korea, and with KYE Pharmaceuticals Inc. for
Canada.
Accrufer®/Feraccru® has patent
coverage until the mid-2030s.
Accrufer®/Feraccru® are registered
trademarks of Shield Therapeutics.
Forward-Looking Statements
This press release contains
forward-looking statements. All statements contained in this press
release that do not relate to matters of historical fact should be
considered forward-looking statements. These forward-looking
statements are based on management's current expectations and
include statements related to the commercial strategy for
Accrufer®/Feraccru®. These statements are neither promises nor
guarantees, but involve known and unknown risks and uncertainties,
many of which are beyond our control, that may cause actual results
and performance or achievements to be materially different from
management's expectations expressed or implied by the
forward-looking statements, including, but not limited to, risks
associated with the Company's business and results of operations,
competition and other market factors. The forward-looking
statements made in this press release represent management's
expectations as of the date of this press release, and except as
required by law, the Company disclaims any obligation to update any
forward-looking statements contained in this release, even if
subsequent events cause its views to change.