hVIVO plc
("hVIVO", the "Company" or
the "Group")
Acquisition of two
Clinical Research Units from CRS for €10.0m
Outlook for 2025 and
2026
·
CRS is a German based full-service early-stage
clinical development CRO
·
First step in hVIVO's M&A strategy and further
diversifies hVIVO's services to include in-patient Phase I and
Phase II trials across a broader range of therapeutic
areas
·
Establishes a significant footprint in Europe with
120 beds across two sites in Germany
·
Total consideration of €10.0 million in cash,
funded from hVIVO's existing cash resources
·
The two units being acquired recorded revenue of
€19.9 million in 2024 (unaudited) and €18.6 million in
2023
·
Acquisition expected to be earnings accretive in
2026
·
Enlarged Group weighted contracted orderbook
of £67 million as at 31 December 2024* following
record delivery of £62.7m revenue by hVIVO in 2024
·
Full year revenue guidance of £73 million in
2025 with EBITDA margins anticipated to be mid-high teens
(excluding one-off costs)
·
Expect to deliver strong growth in revenue in 2026
and a significant improvement on EBITDA margin
*Does not include the
recently announced pivotal Phase 3 HCT for
ILiAD Biotechnologies, expected to be the Group's largest HCT to
date.
Commentary on FY24 results are available
here.
hVIVO plc (AIM: HVO), a
fast-growing early-stage Contract Research Organisation ("CRO") and
the world leader in human challenge clinical trials, announces that it has acquired two Clinical Research Units
("CRUs") from CRS Clinical Research Services Management GmbH
("CRS") (the "Acquisition"), a German full-service early-phase CRO
which provides early clinical development services, including
first-in-human and proof-of-concept trials. The Acquisition has
been completed for a cash consideration of €10.0 million, wholly
funded from the Group's existing cash resources (£44.2 million
(unaudited) as at 31 December 2024).
Details of the Acquisition and strategic
rationale
Founded in 1977 and headquartered in
Mannheim, Germany, CRS has enrolled over 7,700 participants in the
past six years across 260 trials, earning a strong reputation for
quality, safety and excellence. hVIVO has acquired CRS' Mannheim
and Kiel units which accommodate 120 beds in total, with the
Mannheim facility being one of the largest clinical trial
facilities in Germany with 94 beds. CRS' Berlin site will remain an
independent operation, continuing as hVIVO's preferred partner for
specialised clinical trials.
CRS has an extensive and diversified
European client base across pharmaceutical, biotechnology and CRO
businesses, including four of the world's largest 10 biopharma
companies. CRS Mannheim specialises in conducting
cardiometabolic, immunology/inflammation,
and complex PK/PD studies in healthy volunteers, while Kiel is
renowned for its expertise in trials
involving renal and
hepatic impaired patients.
The Acquisition expands hVIVO's
suite of services while also strengthening the Group's existing
service offering. hVIVO will now offer Phase I and in-patient Phase
II clinical trial services including first-in-human, SAD/MAD,
BE/BA, QTc, DDI* and specialist renal and hepatic impairment
trials. The Acquisition brings considerable cross-selling
opportunities for both hVIVO and Venn Life Sciences as well as a
broader client base and more diverse revenue streams. CRS currently
outsources a number of services which the Group will now be able to
provide in-house, such as laboratory, biometry, and consulting
services including CMC, Clinical, PK, as well as regulatory
services. The addition of two new sites in continental Europe gives
the Group international clinical site capabilities for large field
trials and means that it can now offer patient recruitment services
in two of Europe's most highly populated countries with high levels
of clinical trial activity.
In 2024, CRS introduced a new
Business Development team and commercial leadership which has
already had success in building a stronger sales pipeline. With the
diversified full service offering of the new combined Group, the
Company anticipates CRS' sales to continue to drive growth going
forward. The integration of the Business Development teams will
support the multiple cross-selling opportunities that are expected
to be realised from the Acquisition across hVIVO, Venn, and CRS
service offering. As most of the trials conducted by CRS are in
patients, it could provide opportunities to run multi-site trials
across the Group's UK & German sites. hVIVO will also deploy
its core existing systems into CRS to drive efficiencies and
long-term growth.
The current senior leadership team
at CRS, consisting of Dr. Elisabeth Lackner, Chief Executive
Officer; Catherine Canales, Chief Commercial Officer; Prof. Dr.
Thomas Forst, Chief Medical Officer; and Till Mieskes, Chief
Financial Officer, will continue in their roles. They will work
closely with hVIVO's team to implement new initiatives designed to
drive growth and deliver a profitable business by 2026.
Trading history of two units being acquired
The Mannheim and Kiel units recorded
unaudited revenues of €19.9 million in the financial year ended 31
December 2024 (€18.6 million in 2023), with an adjusted EBITDA loss
of €1.8 million (€1.6 million in 2023). Under hVIVO's ownership the
two units will undergo an investment and restructuring programme to
assist with their integration which is expected to cost c.€2.5
million in 2025 including net liabilities being acquired of less
than €0.5 million.
Current year and 2026 outlook
The Company expects to achieve Group
revenues of £73 million in 2025, anticipated to be weighted towards
the second half, representing a robust year-on-year performance of
the core business (excluding the impact of the one-off client
funded facility fee of £4.3 million recognised in 2024) but
including revenues expected to be generated by CRS. The Company
expects to achieve EBITDA margins in the mid-high teens in 2025
(excluding any one-off costs) and remain cash generative. While the
integration of the Acquisition into the wider Group is expected to
impact EBITDA margins in the short term, CRS is expected to be
earnings accretive in 2026. The Group expects to deliver strong
revenue growth in 2026 and a significant improvement on EBITDA
margins following the integration of CRS.
The combined Group entered 2025 with
a pro forma weighted contracted orderbook of £67 million as at 31
December 2024 which stretches into 2026. The weighted contracted
orderbook does not include the recently announced pivotal Phase 3
HCT for ILiAD Biotechnologies, expected to be the Group's largest
HCT to date.
As reported on 10 September 2024,
the Group had a pipeline of short to medium term potential
opportunities of c.£40 million, of which c.£15 million has
already been converted into signed contracts, with c.£25 million
representing active opportunities. In 2024 the Group updated
its challenge agent portfolio and as a result, has seen a
significant rise in interest in its HCT models, with more
opportunities in an advanced stage than at any time in 2024. As an
example, the increased global hMPV infections have increased client
interest in the Company's new hMPV human challenge model. Further
to recently awarded contracts for hLAB and field studies, the
Company expects the growth to continue in these service lines.
Following the Acquisition, average contract sizes across the Group
are anticipated to increase, as well as growth in the CRS sales
pipeline.
The Board is pleased to have
commenced its M&A strategy to further grow and diversify its
revenue streams and to deliver its £100 million Group revenue
target by 2028. The Group will continue to explore further small
bolt-on acquisitions that meet the Company's strategic and
financial criteria.
Yamin 'Mo' Khan, Chief Executive Officer of hVIVO plc,
said: "I am delighted to have completed this acquisition of CRS'
clinical research units at Mannheim and Kiel, aligning with our
M&A strategy to find complementary businesses that can further
broaden our service offering. The acquisition will establish a
significant European footprint for hVIVO, which combined with CRS'
expertise in early clinical development, will create significant
synergies and growth opportunities for the entire
Group.
"CRS is a well-respected brand in the industry providing high
quality services for early-stage clinical development. They are one
of the leading European clinical trial units with a loyal customer
base, a strong team, and a history of delivering consistent
revenues. I look forward to working with the CRS team and
leveraging our combined expertise to deliver growth for the
Group.
"Overall, the mid- and long-term outlook for the Group is
excellent. We have laid foundations for future growth, expanded our
service offerings organically and diversified to a wider range of
revenue streams through the CRS acquisition. As such, I believe we
have significantly strengthened and diversified the business and
have enhanced our ability to deliver our target of growing Group
revenue to £100 million by 2028."
Dr
Elisabeth Lackner, Chief Executive Officer of CRS,
said: "I am delighted that the CRS Mannheim and Kiel units are
joining the hVIVO Group. Together, we can leverage each other's
specialist CRO expertise and complementary infrastructures. CRS'
clinical trial sites seamlessly
enhance hVIVO's site services
offering, and the combined Group will be able to
develop new ways
to
benefit our global client
base."
Analyst briefing
A briefing for
sell-side equity analysts will take place on Wednesday 29 January
2025 at 11.00am GMT. To register and for more details please
contact Walbrook PR on hvivo@walbrookpr.com.
Investor presentation
Yamin 'Mo' Khan, Chief Executive
Officer, and Stephen Pinkerton, Chief Financial Officer, will
provide a live presentation relating to the trading update and
acquisition via the Investor Meet Company platform on
Wednesday 29 January 2025 at 5.00pm
GMT.
Investors can sign up to Investor
Meet Company for free and add to meet hVIVO
here. Investors who already follow hVIVO on
the Investor Meet Company platform will automatically be
invited.
*SAD: Single Ascending Dose, MAD: Multiple Ascending Dose, BE:
Bioequivalence, BA: Bioavailability, QTc: Corrected QT, DDI:
Drug-Drug Interaction.
For
further information please contact:
hVIVO plc
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+44 (0)20
7756 1300
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Yamin 'Mo' Khan, Chief Executive Officer
Stephen Pinkerton, Chief Financial
Officer
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Cavendish Capital Markets Limited (Nominated Adviser and Joint
Broker)
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+44 (0)20
7220 0500
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Geoff Nash, Camilla Hume, Harriet
Ward
Nigel Birks - Life Science
Specialist Sales
Louise Talbot - Sales
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Peel Hunt LLP (Joint Broker)
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+44 (0)20
7418 8900
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James Steel, Dr Christopher Golden
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Davy (Joint Broker)
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+353 (0) 1
679 6363
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Anthony Farrell, Niall
Gilchrist
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Walbrook PR (Financial PR & IR)
Paul McManus / Phillip Marriage
/
Louis Ashe-Jepson
|
+44 (0)20
7933 8780 or hvivo@walbrookpr.com
+44
(0)7980 541 893 / +44 (0)7867 984 082 /
+44 (0)7747 515 393
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The information contained within this announcement is deemed
by the Company to constitute inside information as stipulated under
the Market Abuse Regulation ("MAR") EU no.596/2014. Upon the
publication of this announcement via Regulatory Information Service
("RIS"), this inside information is now considered to be in the
public domain.
Notes to
Editors
hVIVO plc
(Ticker: HVO) is a rapidly growing early-stage Contract Research
Organisation (CRO) and the global leader in human challenge trials.
The company delivers end-to-end clinical development services to a
diverse and expanding client base, including seven of the world's
ten largest biopharma companies.
hVIVO specialises in
conducting human challenge trials across multiple infectious and
respiratory indications, leveraging its state-of-the-art quarantine
facility in London-the largest of its kind worldwide. The company
also offers comprehensive virology and immunology laboratory
services under the hLAB brand.
Through its German
subsidiary, CRS, hVIVO operates a
120-bed capacity across Mannheim and Kiel, providing early-phase
clinical trial services, including first-in-human and
proof-of-concept studies. Its second subsidiary, Venn
Life Sciences, offers Early Drug Development Consulting
and Biometry services to the biopharma sector.
The Group provides fully
integrated drug development solutions from preclinical stages
through Phase II trials, alongside patient recruitment via
FluCamp. Additionally, its five
clinical sites support outpatient Phase II and III trials, ensuring
a seamless and efficient pathway from discovery to late-stage
development.