Pharming Group reports third quarter 2024 financial results and
provides business update
- Third quarter 2024 total
revenues increased by 12% to
US$74.8 million, compared to the third quarter 2023,
driven by continued strong RUCONEST® and Joenja® revenue
growth
- RUCONEST® third quarter
revenue increased by 6% to
US$63.6 million, compared to the third quarter 2023
- Joenja® (leniolisib) third
quarter revenue increased by 72%
to US$11.2 million, compared to the third quarter
2023
- First nine months total
revenues increased by 25% to
US$204.5 million, compared to the first nine months
2023
- On track for
2024 total revenue guidance of US$280 million -
US$295 million (14 - 20% growth)
- Third quarter operating
profit increased to US$4.1 million from US$1.9 million in the third
quarter 2023
- Overall cash and marketable
securities increased to US$173.3 million at the end of the third
quarter 2024 from US$161.8 million at the end of the second quarter
2024
- Sijmen de Vries, our
Executive Director/Chief Executive Officer, has informed the Board
of Directors that he will not be available for reappointment at the
next Annual General Meeting of Shareholders in May
2025
- Pharming to host a
conference call today at 13:30 CEST (7:30 am EDT)
Leiden, the Netherlands, October 24,
2024: Pharming Group N.V. (“Pharming” or “the Company”)
(Euronext Amsterdam: PHARM/NASDAQ: PHAR) presents its preliminary,
unaudited financial report for the three months ended
September 30, 2024.
Chief Executive Officer, Sijmen de
Vries, commented:
“Pharming has delivered an excellent third quarter, increasing
quarterly revenues by 12% to a record-high US$74.8 million and also
achieving record revenues of US$204.5 million for the first nine
months of the year. The combination of strong revenue performance,
combined with reduced operating expenses compared to the previous
quarter, enabled us to realize a positive operating profit in the
third quarter. We are firmly on track to meet our 2024 total
revenue guidance of US$280 million - US$295 million (14 - 20%
growth).
The third quarter demonstrated Pharming’s
ability to deliver continued growth for RUCONEST® in the
competitive U.S. HAE market, with strength in underlying demand
including new patient enrollments. Third quarter revenue for this
product increased by 6% compared to the same quarter in
2023.
For Joenja®, we continue to both increase
the number of patients on therapy quarter-on-quarter and to
maintain high adherence rates for these patients. We received U.K.
approval for Joenja® (leniolisib) in September, demonstrating our
active efforts with regulatory authorities to make this medicine
available to as many patients as possible, and now look forward to
the results of the reimbursement evaluation over the coming
quarters and to a subsequent commercial launch.
In October 2024, we announced the start of a
Phase II, proof of concept, clinical trial evaluating leniolisib in
primary immunodeficiencies (PIDs) with immune dysregulation linked
to PI3Kẟ signaling. This is an important step for Pharming as this
trial will include patients with various PIDs with significant
unmet medical need and much higher overall prevalence than APDS,
including ALPS-FAS, CTLA4 haploinsufficiency, NFKB1
haploinsufficiency and PTEN deficiency. With prevalence of
approximately seven patients per million, these PIDs represent a
potential five-fold increase in the commercial opportunity for
leniolisib, thereby ensuring Pharming is delivering on its mission
to serve the unserved rare disease patient.
I have informed the Board of Directors that
I will not be available, after a 16 year tenure at the helm of
Pharming, for reappointment as Executive Director/Chief Executive
Officer. Our company is in great shape today. So this is the right
moment for me to make way for a successor to lead Pharming into the
next chapter of its strategy for growth, building on the
achievements of the past years. I am proud of all these
achievements and grateful for the trust put in me by our patients,
employees and investors over the years. I will continue to dedicate
myself fully to Pharming until my successor has been appointed and
will do everything in my power to ensure a smooth
hand-over.”
Chairman of the Board of Directors, Dr.
Richard Peters, commented:
“On behalf of the entire Board of Directors, I would like to
thank Sijmen de Vries for his high commitment to Pharming over the
past 16 years and for the way he has created the company that it is
today, serving patients and paving the way for the delivery on the
company’s strategy for growth.
The Board of Directors has engaged a leading
global executive search firm for the search of a successor. Further
announcements will be made when appropriate.
We will of course take time to celebrate
Sijmen’s tenure as our CEO in the coming months.”
Third quarter highlights
Commercialized products
RUCONEST® marketed for the treatment of acute HAE
attacks
RUCONEST® continued to perform well in the third
quarter of 2024, with revenues of US$63.6 million, a 6% increase
compared to the third quarter of 2023. Revenue for the first nine
months of 2024 was US$172.6 million, a 12% increase compared to the
same period in 2023.
The U.S. market contributed 97% of third quarter
revenues, while the EU and Rest of World contributed 3%.
In the U.S. market, we saw continued strength in
the third quarter in underlying in-market demand, including
approximately 100 new patient enrollments. We achieved strong
overall performance in the third quarter in other leading key
revenue indicators including the number of prescribers, the total
number of patients on therapy, and vials shipped to patients.
Increasing enrollments helped to drive a sharp increase in unique
patient shipments in the third quarter.
Joenja® (leniolisib) marketed for the treatment of
APDS
Joenja® revenues increased to US$11.2 million in
the third quarter of 2024, a 72% increase compared to the third
quarter of 2023. This increase was mostly driven by higher volume
from the 50% increase in patients on paid therapy in the U.S.
compared to the third quarter of 2023, and revenues from EU and
Rest of World which are from product provided on a named patient
basis. Revenue for the first nine months of 2024 was US$31.9
million, compared to US$10.3 million for the same period in
2023.
As of September 30, 2024, we have 93 patients on
paid therapy in the U.S. and an additional five patients enrolled
and pending authorization, representing an increase of both active
and pending patients during the third quarter and continued
progress enrolling and moving eligible patients to paid
therapy.
Joenja® (leniolisib) development updates
Leniolisib for APDS
Pharming made continued progress in the third
quarter of 2024 on leniolisib regulatory filings for APDS patients
12 years of age and older in key global markets. Pharming is on
track to complete the manufacturing activities requested by the
European Medicines Agency’s (EMA) Committee for Human Medicinal
Products (CHMP) and submit a response prior to the January 2026
deadline. In addition, Pharming progressed ongoing clinical trials
to support regulatory filings for approval in Japan and pediatric
label expansion beginning in 2025. Data readout from the clinical
trial for children ages 4 to 11 years old is expected in the fourth
quarter of 2024.
In total, there are currently 164 patients in a
leniolisib Expanded Access Program (compassionate use), an ongoing
clinical study, or a named patient program.
United Kingdom
On September 25, 2024, the U.K. Medicines and
Healthcare products Regulatory Agency (MHRA) granted marketing
authorization for Joenja® (leniolisib) for the treatment of APDS in
adult and pediatric patients 12 years of age and older. Joenja® was
the first new medicine approved by the MHRA via the International
Recognition Procedure (IRP) using the U.S. FDA as reference
regulator. Leniolisib is currently under evaluation by the National
Institute for Health and Care Excellence (NICE) regarding
reimbursement within the National Health Service (NHS) in
England.
Leniolisib for additional indications (PI3Kδ platform) -
Primary immunodeficiencies (PIDs) beyond APDS
On October 10, 2024, Pharming announced the
start of a Phase II, proof of concept, clinical trial evaluating
leniolisib in PIDs with immune dysregulation linked to PI3Kẟ
signaling in lymphocytes, with similar clinical phenotypes and
unmet medical needs to APDS. The first patient is expected to be
enrolled in the study in the coming weeks. The clinical trial will
include PID patients with ALPS-FAS, CTLA4 haploinsufficiency, NFKB1
haploinsufficiency and PTEN deficiency, among others. Epidemiology
suggests a prevalence of approximately seven patients per million
in this targeted PID population, compared to one to two patients
per million for APDS.
The Phase II clinical trial is a single arm,
open-label, dose range-finding study to be conducted in
approximately 12 patients. The objectives for the trial will be to
assess safety and tolerability, pharmacokinetics, pharmacodynamics,
and explore clinical efficacy of leniolisib in the targeted PID
population. The trial has been designed to inform a subsequent
Phase III program.
Pharming has also prioritized development of
leniolisib for an additional PID indication. Pharming will provide
further updates and details on our plans, including the proposed
clinical development plan, later this year.
Organizational update
Sijmen de Vries, our Executive Director/Chief
Executive Officer, has informed the Board of Directors that he will
not be available for reappointment at the Company’s next Annual
General Meeting of Shareholders (AGM) in May 2025. The mandate of
Sijmen de Vries is scheduled to expire at the closing of the AGM to
be held in May 2025. Further announcements on the search of a
successor will be made when appropriate.
Financial Summary
Consolidated Statement of Income |
3Q 2024 |
3Q 2023 |
9M 2024 |
9M 2023 |
Amounts in US$m except per share data |
|
|
|
|
Total Revenues |
74.8 |
66.7 |
204.5 |
164.1 |
Cost of sales |
(6.8) |
(8.3) |
(23.2) |
(18.1) |
Gross profit |
68.0 |
58.4 |
181.3 |
146.0 |
Other income |
0.8 |
0.3 |
2.1 |
22.8 |
Research and development |
(20.7) |
(20.8) |
(60.8) |
(57.3) |
General and administrative |
(15.3) |
(10.9) |
(46.0) |
(31.9) |
Marketing and sales |
(28.7) |
(25.1) |
(91.9) |
(86.1) |
Other Operating Costs |
(64.7) |
(56.8) |
(198.7) |
(175.3) |
Operating profit (loss) |
4.1 |
1.9 |
(15.3) |
(6.5) |
Finance income (expense) and share of net profits in
associates |
(2.6) |
1.4 |
0.1 |
(3.5) |
Profit (loss) before tax |
1.5 |
3.3 |
(15.2) |
(10.0) |
Income tax credit (expense) |
(2.5) |
0.2 |
0.5 |
2.6 |
Profit (loss) for the period |
(1.0) |
3.5 |
(14.7) |
(7.4) |
Share Information |
|
|
|
|
Basic earnings per share (US$) |
(0.002) |
0.005 |
(0.022) |
(0.011) |
Diluted earnings per share (US$) |
(0.002) |
0.005 |
(0.022) |
(0.011) |
Segment information - Revenues |
3Q 2024 |
3Q 2023 |
9M 2024 |
9M 2023 |
Amounts in US$m |
|
|
|
|
Revenue - RUCONEST® (US) |
62.0 |
58.4 |
168.4 |
149.3 |
Revenue - RUCONEST® (EU and RoW) |
1.6 |
1.8 |
4.2 |
4.5 |
Total Revenues - RUCONEST® |
63.6 |
60.2 |
172.6 |
153.8 |
Revenue - Joenja® (US) |
10.0 |
6.5 |
28.7 |
10.3 |
Revenue - Joenja® (EU and RoW) |
1.2 |
— |
3.2 |
— |
Total Revenues - Joenja® |
11.2 |
6.5 |
31.9 |
10.3 |
|
|
|
|
|
Total Revenues - US |
72.0 |
64.9 |
197.1 |
159.6 |
Total Revenues - EU and RoW |
2.8 |
1.8 |
7.4 |
4.5 |
|
|
|
|
|
Total Revenues |
74.8 |
66.7 |
204.5 |
164.1 |
Consolidated Balance Sheet |
September 30, 2024 |
December 31, 2023 |
Amounts in US$m |
|
|
Cash and cash equivalents, restricted cash and marketable
securities |
173.3 |
215.0 |
Current assets |
282.2 |
316.3 |
Total assets |
425.5 |
462.9 |
Current liabilities |
79.8 |
78.0 |
Equity |
225.8 |
218.8 |
Financial highlights
Third quarter 2024
For the third quarter of 2024, total revenues
increased by US$8.2 million, or 12%, to US$74.8 million, compared
to US$66.7 million in the third quarter of 2023. RUCONEST® revenues
amounted to US$63.6 million, a 6% increase compared to the third
quarter of 2023. The volume increase in the U.S., and a U.S. price
increase in line with CPI, were the primary factors behind this
increase in RUCONEST® revenues. Joenja® revenues amounted to
US$11.2 million in the third quarter of 2024, a 73% increase
compared to the third quarter of 2023. This increase was primarily
driven by an increase in volume.
Gross profit increased by US$9.7 million or 17%
to US$68.0 million (3Q 2023: US$58.4 million), mainly due to the
increase in revenues.
The operating profit amounted to US$4.1 million
compared to an operating profit of US$1.9 million in the third
quarter of 2023. This increase was primarily due to the increase in
gross profit mentioned above, offset by the increase in operating
expenses from US$56.8 million in the third quarter of 2023 to
US$64.7 million. The increase in operating expenses compared to the
same quarter in 2023 was caused by a combination of continuing
investments in Joenja® in the U.S., launch preparation for
leniolisib outside of the U.S., increasing R&D investments to
expand the leniolisib franchise and increased payroll expenses due
to business growth. Third quarter 2024 operating expenses decreased
8% from US$70.1 million in the second quarter of 2024.
The net finance result amounted to a loss of
US$2.2 million compared to a gain of US$1.9 million in the third
quarter of 2023. This was primarily driven by unfavorable EUR/USD
exchange rate developments, resulting in a foreign currency loss of
US$1.5 million compared to a gain of US$1.7 million in the third
quarter of 2023. Additionally, interest expense increased by US$1.0
million in the third quarter of 2024 compared to the previous year,
following the convertible bond issuance in the second quarter of
2024.
The Company had a net loss of US$1.0 million,
compared to a net profit of US$3.5 million in the third quarter of
2023. This change was mainly due to higher finance expense
resulting from unfavorable EUR/USD exchange rate developments and
higher income tax expenses, despite higher operating profit. While
the exchange rate fluctuations resulted in a foreign currency loss
in the income statement, currency translation differences in other
comprehensive income led to a positive result of US$2.9 million,
compared to a negative result of US$5.2 million in the third
quarter of 2023. This outcome was driven by the Company’s
predominantly euro-denominated assets, including the vast majority
of the cash and marketable securities position.
Cash and cash equivalents, including restricted
cash and marketable securities, increased from US$161.8 million at
the end of second quarter of 2024 to US$173.3 million at the end of
the third quarter of 2024. This increase was primarily driven by
positive cash flows from operations of US$9.7 million (3Q 2023:
US$3.5 million), which includes a deduction of US$9.1 million in
paid taxes (3Q 2023: US$0.0 million).
Nine months 2024
Total revenues increased 25% during the first
nine months of 2024 to US$204.5 million, versus US$164.1 million
during the first nine months of 2023. Total RUCONEST® revenues were
12% higher at US$172.6 million, compared to revenues of US$153.8
million for the first nine months of 2023. Joenja® revenues
amounted to US$31.9 million in the first nine months of 2024, a
210% increase compared to the first nine months of 2023 (first
sales commenced at the start of the second quarter of 2023). This
increase was primarily driven by an increase in volume.
Gross profit increased by US$35.3 million or 24%
to US$181.3 million (9M 2023: US$146.0 million), mainly due to the
increase in revenues.
Other income decreased to US$2.0 million
compared to US$22.8 million in the first nine months of 2023. Other
income in the first nine months of 2023 was supported by the sale
of the Rare Pediatric Disease Priority Review Voucher (PRV) to
Novartis for a pre-agreed, one-time payment of US$21.1 million.
The operating loss amounted to US$15.3 million
compared to an operating loss of US$6.5 million in the first nine
months of 2023. This change was mainly due to the decrease in other
income and the expected increase in operating expenses from
US$175.3 million in the first nine months of 2023 to US$198.7
million, offset by the above mentioned increase in gross profit in
the first nine months of 2024. The first nine months of 2023
operating expenses included milestone payments for Joenja® of
US$10.5 million in the second quarter. The increase in operating
expenses in the first nine months of 2024 was caused by a
combination of continuing investments in Joenja® in the U.S.,
launch preparation for leniolisib outside of the U.S., increasing
R&D investments to expand the leniolisib franchise and
increased payroll expenses due to business growth. Excluding the
one time proceeds from the PRV sale and the milestone payment
expenses for Joenja® in the first nine months of 2023, the
operating loss decreased from US$17.1 million to US$15.3 million in
the first nine months of the current year.
The net finance result amounted to a gain of
US$1.4 million compared to a loss of US$2.6 million in the first
nine months of 2023. This was primarily driven by a fair value gain
of US$5.2 million upon the reclassification of the convertible
bond-related derivative to equity. This fair value gain was a
result of the decrease in value of the option component classified
as a derivative from issuance until the physical settlement date of
the newly issued convertible bond. In addition, interest income
from investments in marketable securities, which commenced in the
second quarter of 2023, increased by US$1.7 million. These positive
results were partially offset by US$1.1 million higher interest
expense on the 2024 issued convertible bond and unfavorable EUR/USD
exchange rate developments, which led to a foreign currency loss of
US$1.3 million compared to a loss of US$0.1 million in the first
nine months of 2023.
The Company had a net loss of US$14.7 million,
compared to a net loss of US$7.4 million in the first nine months
of 2023. In addition to the support in other income from the PRV
and the milestone payments for Joenja® in the first nine months of
2023, the change was mainly due to an increase in gross profit,
higher interest income and the fair value gain upon the
reclassification of the convertible bond-related derivative to
equity, offset by an increase in operating expenses, unfavorable
EUR/USD exchange rate developments and higher interest expenses on
the 2024 issued convertible bond.
Cash and cash equivalents, including restricted
cash and marketable securities, decreased from US$215.0 million at
the end of 2023 to US$173.3 million at the end of September 2024.
This decrease was primarily driven by the repurchase of the
outstanding convertible bonds amounting to US$134.9 million and
paid taxes of US$13.9 million, offset by net proceeds of US$104.5
million for newly issued convertible bonds.
On 5 October 2023, Orchard Therapeutics Plc.
(Orchard) announced it had entered into a definitive agreement with
Japanese company Kyowa Kirin Co. LTD for the acquisition of
Orchard. During the first nine months of 2024, Pharming received
US$2.0 million in cash for its shares held in Orchard. Pharming has
terminated the research collaboration & licensing agreement
with Orchard Therapeutics and discontinued the OTL-105 program.
Outlook/Summary
For the remainder of 2024 and the full year, the
Company anticipates:
- Total revenues between US$280
million and US$295 million (14% to 20% growth).
- Continued progress finding
additional APDS patients in the U.S., supported by family testing
and VUS validation efforts, and subsequently converting patients to
paid Joenja® (leniolisib) therapy.
- Increasing leniolisib ex-U.S.
revenues - through our Named Patient Program and other funded early
access programs in key global markets.
- Completion of leniolisib clinical
trials to support regulatory filings for approval in Japan and
pediatric label expansion in key global markets.
- Progress towards regulatory
approvals for leniolisib in the EEA, Canada and Australia.
- Advancing the Phase II clinical
trial for leniolisib in PIDs with immune dysregulation linked to
PI3Kδ signaling to significantly expand the long-term commercial
potential of leniolisib.
- Continued focus on potential
acquisitions and in-licensing of clinical stage opportunities in
rare diseases. Financing, if required, would come via a combination
of our strong balance sheet and access to capital markets.
No further specific financial guidance for 2024
is provided.
Additional information
Presentation
The conference call presentation is available on
the Pharming.com website from 07:30 CEST today.
Conference Call
The conference call will begin at 13:30
CEST/07:30 EDT on Thursday, October 24. A transcript will be made
available on the Pharming.com website in the days following the
call.
Please note, the Company will only take
questions from dial-in attendees.
Webcast Link:
https://edge.media-server.com/mmc/p/yotjk8ib
Conference call dial-in details:
https://register.vevent.com/register/BId118ac68d9124f67b1a83e3769559100
Additional information on how to register for the conference
call/webcast can be found on the Pharming.com website.
For further public information, contact:
Pharming Group N.V., Leiden, the
Netherlands
Michael Levitan, VP Investor Relations & Corporate
Communications
T: +1 (908) 705 1696
E: investor@pharming.com
FTI Consulting, London, UK
Victoria Foster Mitchell/Alex Shaw
T: +44 203 727 1000
LifeSpring Life Sciences Communication,
Amsterdam, the Netherlands
Leon Melens
T: +31 6 53 81 64 27
E: pharming@lifespring.nl
About Pharming Group N.V.
Pharming Group N.V. (EURONEXT Amsterdam:
PHARM/Nasdaq: PHAR) is a global biopharmaceutical company dedicated
to transforming the lives of patients with rare, debilitating, and
life-threatening diseases. Pharming is commercializing and
developing an innovative portfolio of protein replacement therapies
and precision medicines, including small molecules and biologics.
Pharming is headquartered in Leiden, the Netherlands, and has
employees around the globe who serve patients in over 30 markets in
North America, Europe, the Middle East, Africa, and
Asia-Pacific.
For more information, visit www.pharming.com and
find us on LinkedIn.
Auditor’s involvement
The Condensed Consolidated Interim Financial
Statements have not been audited by the Company’s statutory
auditor.
Forward-looking Statements
This press release may contain
forward-looking statements. Forward-looking statements are
statements of future expectations that are based on management’s
current expectations and assumptions and involve known and unknown
risks and uncertainties that could cause actual results,
performance, or events to differ materially from those expressed or
implied in these statements. These forward-looking statements are
identified by their use of terms and phrases such as “aim”,
“ambition”, ‘‘anticipate’’, ‘‘believe’’, ‘‘could’’, ‘‘estimate’’,
‘‘expect’’, ‘‘goals’’, ‘‘intend’’, ‘‘may’’, “milestones”,
‘‘objectives’’, ‘‘outlook’’, ‘‘plan’’, ‘‘probably’’, ‘‘project’’,
‘‘risks’’, “schedule”, ‘‘seek’’, ‘‘should’’, ‘‘target’’, ‘‘will’’
and similar terms and phrases. Examples of forward-looking
statements may include statements with respect to timing and
progress of Pharming's preclinical studies and clinical trials of
its product candidates, Pharming's clinical and commercial
prospects, and Pharming's expectations regarding its projected
working capital requirements and cash resources, which statements
are subject to a number of risks, uncertainties and assumptions,
including, but not limited to the scope, progress and expansion of
Pharming's clinical trials and ramifications for the cost thereof;
and clinical, scientific, regulatory, commercial, competitive and
technical developments. In light of these risks and uncertainties,
and other risks and uncertainties that are described in Pharming's
2023 Annual Report and the Annual Report on Form 20-F for the year
ended December 31, 2023, filed with the U.S. Securities and
Exchange Commission, the events and circumstances discussed in such
forward-looking statements may not occur, and Pharming's actual
results could differ materially and adversely from those
anticipated or implied thereby. All forward-looking statements
contained in this press release are expressly qualified in their
entirety by the cautionary statements contained or referred to in
this section. Readers should not place undue reliance on
forward-looking statements. Any forward-looking statements speak
only as of the date of this press release and are based on
information available to Pharming as of the date of this release.
Pharming does not undertake any obligation to publicly update or
revise any forward-looking statement as a result of new
information, future events or other information.
Inside Information
This press release relates to the disclosure of information
that qualifies, or may have qualified, as inside information within
the meaning of Article 7(1) of the EU Market Abuse
Regulation.
Pharming Group N.V.
Condensed Consolidated Interim Financial
Statements in US Dollars (unaudited)
For the period ended September 30, 2024
- Condensed consolidated interim
statement of income
- Condensed consolidated interim
statement of comprehensive income
- Condensed consolidated interim
balance sheet
- Condensed consolidated interim
statement of changes in equity
- Condensed consolidated interim
statement of cash flows
CONDENSED CONSOLIDATED INTERIM STATEMENT OF
INCOME |
For the
period ended September 30 |
|
Amounts in US$ ‘000 |
3Q 2024 |
3Q 2023 |
9M 2024 |
9M 2023 |
Revenues |
74,849 |
66,661 |
204,528 |
164,099 |
Costs of sales |
(6,819) |
(8,295) |
(23,186) |
(18,094) |
Gross profit |
68,030 |
58,366 |
181,342 |
146,005 |
Other income |
777 |
304 |
2,034 |
22,811 |
Research and development |
(20,721) |
(20,753) |
(60,839) |
(57,287) |
General and administrative |
(15,292) |
(10,886) |
(45,999) |
(31,849) |
Marketing and sales |
(28,686) |
(25,123) |
(91,863) |
(86,136) |
Other Operating Costs |
(64,699) |
(56,762) |
(198,701) |
(175,272) |
Operating profit (loss) |
4,108 |
1,908 |
(15,325) |
(6,456) |
Fair value gain (loss) on revaluation |
21 |
— |
5,159 |
— |
Other finance income |
825 |
1,251 |
3,760 |
2,050 |
Other finance expenses |
(2,998) |
633 |
(7,488) |
(4,621) |
Finance result, net |
(2,152) |
1,884 |
1,431 |
(2,571) |
Share of net profits (loss) in associates using the equity
method |
(442) |
(485) |
(1,276) |
(954) |
Profit (loss) before tax |
1,514 |
3,307 |
(15,170) |
(9,981) |
Income tax credit (expense) |
(2,548) |
157 |
470 |
2,556 |
Profit (loss) for the period |
(1,034) |
3,464 |
(14,700) |
(7,425) |
Basic earnings per share (US$) |
(0.002) |
0.005 |
(0.022) |
(0.011) |
Diluted earnings per share (US$) |
(0.002) |
0.005 |
(0.022) |
(0.011) |
CONDENSED CONSOLIDATED INTERIM STATEMENT OF COMPREHENSIVE
INCOME |
For the
period ended September 30 |
|
Amounts in US$ ‘000 |
3Q 2024 |
3Q 2023 |
9M 2024 |
9M 2023 |
Profit (loss) for the period |
(1,034) |
3,464 |
(14,700) |
(7,425) |
Currency translation differences |
2,883 |
(5,158) |
(1,352) |
(2,079) |
Items that may be subsequently reclassified to profit or
loss |
2,883 |
(5,158) |
(1,352) |
(2,079) |
Fair value remeasurement investments |
1 |
281 |
79 |
419 |
Items that shall not be subsequently reclassified to profit
or loss |
1 |
281 |
79 |
419 |
Other comprehensive income (loss), net of tax |
2,884 |
(4,877) |
(1,273) |
(1,660) |
Total comprehensive income (loss) for the
period |
1,850 |
(1,413) |
(15,973) |
(9,085) |
CONDENSED
CONSOLIDATED INTERIM BALANCE SHEET |
|
|
|
|
|
Amounts in US$ ‘000 |
September 30, 2024 |
December 31, 2023 |
Non-current assets |
|
|
Intangible assets |
67,096 |
71,267 |
Property, plant and equipment |
8,692 |
9,689 |
Right-of-use assets |
21,975 |
23,777 |
Long-term prepayments |
93 |
92 |
Deferred tax assets |
36,752 |
29,761 |
Investment accounted for using the equity method |
1,016 |
2,285 |
Investments in equity instruments designated as at FVTOCI |
— |
2,020 |
Investment in debt instruments designated as at FVTPL |
6,150 |
6,093 |
Restricted cash |
1,548 |
1,528 |
Total non-current assets |
143,322 |
146,512 |
Current assets |
|
|
Inventories |
62,227 |
56,760 |
Trade and other receivables |
48,199 |
46,158 |
Marketable securities |
111,104 |
151,683 |
Cash and cash equivalents |
60,662 |
61,741 |
Total current assets |
282,192 |
316,342 |
Total assets |
425,514 |
462,854 |
Equity |
|
|
Share capital |
7,750 |
7,669 |
Share premium |
487,079 |
478,431 |
Other reserves |
9,334 |
(2,057) |
Accumulated deficit |
(278,371) |
(265,262) |
Shareholders’ equity |
225,792 |
218,781 |
Non-current liabilities |
|
|
Convertible bonds |
92,099 |
136,598 |
Lease liabilities |
27,784 |
29,507 |
Total non-current liabilities |
119,883 |
166,105 |
Current liabilities |
|
|
Convertible bonds |
3,319 |
1,824 |
Trade and other payables |
72,638 |
72,528 |
Lease liabilities |
3,882 |
3,616 |
Total current liabilities |
79,839 |
77,968 |
Total equity and liabilities |
425,514 |
462,854 |
CONDENSED CONSOLIDATED INTERIM STATEMENT OF CHANGES IN
EQUITY |
For the
period ended September 30 |
Attributable to owners of the parent |
|
|
|
|
|
|
Amounts in US$ ‘000 |
Share capital |
Share premium |
Other reserves |
Accumulated deficit |
Total equity |
Balance at January 1, 2023 |
7,509 |
462,297 |
(8,737) |
(256,431) |
204,638 |
Profit (loss) for the period |
— |
— |
— |
(7,425) |
(7,425) |
Reserves |
— |
— |
— |
— |
— |
Other comprehensive income (loss) for the period |
— |
— |
(1,660) |
— |
(1,660) |
Total comprehensive income (loss) for the
period |
— |
— |
(1,660) |
(7,425) |
(9,085) |
Other reserves |
— |
— |
(518) |
518 |
— |
Income tax benefit from excess tax deductions related to
share-based payments |
— |
— |
— |
574 |
574 |
Share-based compensation |
— |
— |
— |
5,935 |
5,935 |
Options exercised / LTIP shares issued |
141 |
13,686 |
— |
(5,947) |
7,880 |
Value of conversion rights of convertible bonds |
— |
— |
— |
— |
— |
Total transactions with owners, recognized directly in
equity |
141 |
13,686 |
(518) |
1,080 |
14,389 |
Balance at September 30, 2023 |
7,650 |
475,983 |
(10,915) |
(262,776) |
209,942 |
|
|
|
|
|
|
Balance at January 1, 2024 |
7,669 |
478,431 |
(2,057) |
(265,262) |
218,781 |
Profit (loss) for the period |
— |
— |
— |
(14,700) |
(14,700) |
Reserves |
— |
— |
1,560 |
(1,560) |
— |
Other comprehensive income (loss) for the period |
— |
— |
(1,273) |
— |
(1,273) |
Total comprehensive income (loss) for the
period |
— |
— |
287 |
(16,260) |
(15,973) |
Other reserves |
— |
— |
(31) |
31 |
— |
Income tax benefit from excess tax deductions related to
share-based payments |
— |
— |
— |
(241) |
(241) |
Share-based compensation |
— |
— |
— |
8,605 |
8,605 |
Options exercised / LTIP shares issued |
81 |
8,648 |
— |
(5,244) |
3,485 |
Value of conversion rights of convertible bonds |
— |
— |
11,135 |
— |
11,135 |
Total transactions with owners, recognized directly in
equity |
81 |
8,648 |
11,104 |
3,151 |
22,984 |
Balance at September 30, 2024 |
7,750 |
487,079 |
9,334 |
(278,371) |
225,792 |
CONDENSED CONSOLIDATED INTERIM STATEMENT OF CASH
FLOWS |
For
the period ended September 30 |
|
Amounts in $’000 |
3Q 2024 |
3Q 2023 |
9M 2024 |
9M 2023 |
Profit (loss) before tax |
1,514 |
3,307 |
(15,170) |
(9,981) |
Adjustments to reconcile net profit (loss) to net cash
used in operating activities: |
|
|
|
|
Depreciation, amortization, impairment of non-current assets |
2,743 |
2,902 |
8,371 |
8,370 |
Equity settled share based payments |
2,918 |
1,965 |
8,605 |
5,935 |
Fair value loss (gain) on revaluation |
(21) |
— |
(5,159) |
— |
Gain on disposal from PRV sale |
— |
— |
— |
(21,080) |
Other finance income |
(182) |
(1,251) |
(3,117) |
(2,050) |
Other finance expenses |
2,315 |
(633) |
6,765 |
4,621 |
Share of net result in associates using the equity method |
442 |
485 |
1,276 |
954 |
Other |
— |
1,055 |
— |
(1,130) |
Operating cash flows before changes in working
capital |
9,729 |
7,830 |
1,571 |
(14,361) |
Changes in working capital: |
|
|
|
|
Inventories |
(2,133) |
(396) |
(5,248) |
(11,113) |
Trade and other receivables |
2,919 |
(7,363) |
(2,044) |
(12,902) |
Payables and other current liabilities |
6,560 |
3,242 |
4,305 |
8,075 |
Restricted cash |
— |
(47) |
— |
363 |
Total changes in working capital |
7,346 |
(4,563) |
(2,987) |
(15,577) |
|
|
|
|
|
Interest received |
1,784 |
260 |
4,154 |
1,059 |
Income taxes received (paid) |
(9,117) |
— |
(13,864) |
— |
Net cash flows generated from (used in) operating
activities |
9,742 |
3,527 |
(11,126) |
(28,879) |
|
|
|
|
|
Capital expenditure for property, plant and equipment |
(366) |
(147) |
(660) |
(1,133) |
Proceeds on PRV sale |
— |
— |
— |
21,080 |
Investment intangible assets |
— |
23 |
— |
23 |
Disposal of investment designated as at FVOCI |
8 |
— |
1,972 |
— |
Purchases of marketable securities |
(109,796) |
(144,554) |
(222,249) |
(231,901) |
Proceeds from sale of marketable securities |
114,504 |
86,451 |
262,345 |
86,451 |
Net cash flows generated from (used in) investing
activities |
4,350 |
(58,227) |
41,408 |
(125,480) |
|
|
|
|
|
Payment of lease liabilities |
(918) |
(1,007) |
(2,485) |
(3,022) |
Interests on lease liabilities |
(258) |
(270) |
(784) |
(825) |
Net proceeds of issued convertible bonds |
(263) |
— |
104,539 |
— |
Repurchase of convertible bonds |
(9) |
— |
(134,931) |
— |
Interests on convertible bonds |
(8) |
(2,029) |
(2,032) |
(4,052) |
Settlement of share based compensation awards |
23 |
8,546 |
3,485 |
7,880 |
Net cash flows generated from (used in) financing
activities |
(1,433) |
5,240 |
(32,208) |
(19) |
|
|
|
|
|
Increase (decrease) of cash |
12,659 |
(49,460) |
(1,926) |
(154,378) |
Exchange rate effects |
861 |
(913) |
847 |
1,689 |
Cash and cash equivalents at the beginning of the period |
47,142 |
105,026 |
61,741 |
207,342 |
|
|
|
|
|
Total cash and cash equivalents at September
30 |
60,662 |
54,653 |
60,662 |
54,653 |
- Pharming reports 3Q24 financial results_EN_24OCT24
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