Pharming Group reports fourth quarter and full year 2023 financial results
- Total revenues increased by 19% to US$245.3 million in 2023.
- RUCONEST® revenues grew by 10% to US$227.1 million.
- Joenja® (leniolisib) had a successful launch with revenues of US$18.2 million in 2023.
- Cash and marketable securities increased to US$215.0 million by the end of 2023.
- Pharming provided a revenue guidance of US$280 million – US$295 million for 2024.
- None.
Insights
The reported increase in total revenues by 19% to US$245.3 million for the full year 2023, with a notable 10% increase in RUCONEST® revenues, is a strong indicator of the company's growth trajectory. The introduction of Joenja® (leniolisib) and its subsequent uptake, with 81 patients on paid therapy in the U.S. and full year revenues of US$18.2 million, demonstrates the company's successful market penetration and diversification strategy. The overall increase in cash and marketable securities to US$215.0 million provides a cushion for future R&D investment and operational flexibility.
Looking ahead, the 2024 revenue guidance of US$280 million – US$295 million, which represents 14% – 20% growth, suggests confidence in the continued demand for RUCONEST® and the expansion of leniolisib's market presence. This forecast could be a positive signal for investors, indicating sustainable growth potential. However, it is essential to monitor the progress of ongoing regulatory reviews and commercialization efforts in additional geographies, as they will be crucial in achieving this growth. The successful expansion of leniolisib for additional primary immunodeficiencies (PIDs) could further drive long-term value creation.
The mention of leniolisib's development for activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) in additional geographies and pediatric patients, as well as its indication expansion to other PIDs, is indicative of the company's commitment to address unmet medical needs in rare diseases. The APDS patient finding initiatives and VUS resolution are critical for increasing the patient base eligible for treatment, which could directly impact future revenues and market share.
Moreover, the orphan drug designation (ODD) by Japan for leniolisib and the initiation of pediatric clinical trials are strategic moves to broaden the treatment's label and market reach. The company's engagement with regulatory authorities like the US FDA and EMA and its submissions for marketing authorization in various countries, reflect a proactive approach to securing approval in multiple markets, potentially leading to a diversified and stable revenue stream.
The competitive landscape of the Hereditary Angioedema (HAE) market and the rare disease sector, in general, is highly specialized, with significant barriers to entry due to the complexity of drug development and the necessity for targeted patient finding strategies. Pharming's strong performance with RUCONEST® in the HAE market and its strategic initiatives to identify and diagnose APDS patients position it favorably within this niche market. The company's ability to grow its prescriber base and patient enrollments, despite the competitive environment, indicates effective marketing and sales strategies.
Furthermore, the company's plans to develop leniolisib for additional PIDs based on the PI3Kδ signaling pathway showcase its intent to leverage its expertise and existing platforms to tap into new market segments. This could potentially lead to the creation of new revenue streams and increase the company's market share within the rare disease space. However, the success of these initiatives will depend on the outcomes of clinical trials and regulatory approvals, which are inherently uncertain and can impact market expectations.
- Full year 2023 total revenues increased by
19% to US$245.3 million - Record fourth quarter RUCONEST® revenues of US
$73.3 million resulted in a10% increase in full year 2023 RUCONEST® revenues to US$227.1 million - Strong start to Joenja® (leniolisib) launch with 81 patients on paid therapy in the U.S. nine months following launch and full year 2023 revenues of US
$18.2 million - Overall cash and marketable securities increased to US
$215.0 million at the end of 2023 from US$208.7 million at the end of 2022
- Progressed leniolisib development for APDS in additional geographies and for pediatric patients, and leniolisib indication expansion to primary immunodeficiencies (PIDs) with immune dysregulation linked to PI3Kδ signaling
- 2024 total revenue guidance of US
$280 million – US$295 million (14% –20% growth) - Pharming to host a conference call today at 13:30 CET (8:30 am EDT)
Leiden, The Netherlands, March 14, 2024: Pharming Group N.V. (“Pharming” or “the Company”) (Euronext Amsterdam: PHARM / Nasdaq: PHAR) presents its preliminary (unaudited) financial report for the three months and full year ended December 31, 2023.
Chief Executive Officer, Sijmen de Vries commented:
“We are pleased to have delivered an excellent year in which we transformed Pharming into a multi-product, commercial rare disease biopharmaceutical company. We grew RUCONEST® revenues by
We launched Joenja® (leniolisib) for APDS in the U.S. in April 2023, shortly after FDA approval, and saw meaningful initial uptake for what is the first and only FDA approved treatment for APDS. We have identified and confirmed over 840 APDS patients in global markets, including over 200 in the U.S. We have started family genetic testing initiatives, important since the majority of APDS patients will have family members also afflicted with the disease. In addition we have commenced studies to determine which of more than 1,100 patients in the U.S., with inconclusive genetic testing results showing a variant of uncertain significance (VUS), have genetic variants that cause hyperactivity in the PI3Kẟ pathway and can, therefore, be classified as APDS disease causing. This allows for an important APDS diagnosis for these patients, who could potentially be eligible for and offered treatment with Joenja®.
We also made strong progress preparing for the commercialization of leniolisib in key global markets. We have been receiving requests for individual treatment on a named patient basis, in markets outside of the U.S., and provided the first patients with leniolisib around year-end 2023. Numerous regulatory reviews are ongoing and we are preparing for commercialization in key global markets including Europe, the U.K., Japan, Asia Pacific, Middle East, and Canada.
These results reflect Pharming’s dedication to developing and delivering therapies to unserved rare disease patients. Looking to 2024, we remain focused on our goals of identifying additional APDS patients globally, continuing the momentum for Joenja® revenue in the U.S., to obtaining regulatory approvals and bringing leniolisib to APDS patients in need of treatment in additional global markets and to further developing our rare disease pipeline and footprint. We are also seeking to significantly expand the leniolisib market opportunity and revenue growth by pursuing development of leniolisib for additional primary immunodeficiencies (PIDs) beyond APDS, and have advanced plans to start a Phase 2 proof of concept clinical trial in PIDs with immune dysregulation linked to PI3Kẟ signaling.”
Fourth quarter and full year 2023 highlights
Commercialized assets
RUCONEST® marketed for the treatment of acute HAE attacks
RUCONEST® performed strongly in the fourth quarter of 2023, with record revenues of US
The U.S. market contributed
The RUCONEST® revenue acceleration in the second half of 2023 can be attributed to strong performance in leading key revenue indicators in the U.S. including new physicians prescribing RUCONEST®, new patient enrollments including high frequency attack patients, and the total number of patients. We achieved over 70 RUCONEST® new patient enrollments for four quarters in a row. Total enrollments in 2023 were up
Joenja® (leniolisib) marketed in the U.S. - the first and only approved disease modifying treatment for APDS
Joenja® (leniolisib) received U.S. FDA approval in late March 2023 for the treatment of activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS) in patients 12 years of age and older, and first commercial shipments to patients took place in April 2023. During the nine months following launch, Pharming made strong and rapid progress transitioning known patients onto commercial therapy.
Revenues increased to US
As of December 31, 2023, we have 92 APDS patients enrolled in the U.S., of which 81 patients are on paid therapy.
APDS patient finding
Based on available literature, Pharming estimates APDS prevalence of 1.5 patients per million. Our U.S. and global APDS patient finding efforts progressed during the year and as of December 31, 2023, Pharming has identified over 840 diagnosed APDS patients of all ages in global markets, including over 200 patients in the U.S. Of the identified patients in the U.S., approximately
Pharming advanced several initiatives during 2023 to diagnose additional APDS patients, including a sponsored genetic testing program in the U.S., partnerships with several genetic testing companies who undertake their own testing efforts and family testing programs. We have initiated a number of programs collaborating with clinicians and patients to aid in reducing the barriers and allowing the appropriate testing in families with APDS, to help identify family members of APDS patients who may also be affected by this disease. APDS is an inherited genetic disease and Pharming believes that many of the over 200 APDS patients already identified in the U.S. are likely to have family members who remain undiagnosed.
APDS patient finding - Variant of Uncertain Significance (VUS) resolution
APDS is diagnosed based on clinical symptoms, assessment of immune cell function and genetic testing. For a patient to receive a definitive APDS diagnosis, a genetic test revealing a disease-causing (pathogenic or likely pathogenic) variant in either the PIK3CD or PIK3R1 genes is required. Patients with clinical symptoms compatible with APDS frequently receive inconclusive genetic variant test results, i.e. previously unseen variants in the PIK3CD or PIK3R1 genes. It is important to determine if these Variants of Uncertain Significance (VUS) cause APDS.
As of December 31, 2023, Pharming has identified more than 1,100 patients in the U.S. with a number of VUSs in the PIK3CD or PIK3R1 genes and is setting up validation studies with various laboratories to confirm which of these variants should be classified as APDS. As results become available, patients with validated variants could be diagnosed with APDS and, therefore, potentially be eligible for Joenja® treatment. Completion of these studies is expected during the fourth quarter of 2024.
Leniolisib highlights - regulatory, clinical and commercial strategy updates
Leniolisib for APDS
Pharming made continued progress in the fourth quarter of 2023 on leniolisib regulatory filings for APDS patients 12 years of age and older in key global markets. In addition, Pharming progressed ongoing clinical trials to support regulatory filings for approval in Japan and pediatric label expansion in key global markets.
Pharming’s strategy is to make leniolisib commercially available for APDS patients in additional key markets in Europe, U.K., Japan, Asia Pacific, Middle East, and Canada. Pharming intends to market leniolisib directly in most of these markets following regulatory approval.
We currently have 96 patients on leniolisib therapy as part of an Expanded Access Program (compassionate use) or an ongoing clinical study. In addition, Pharming makes leniolisib available on a named patient basis to ensure that physicians can request leniolisib on behalf of individual patients living with APDS, who meet the eligibility criteria and receive local health authority authorization, in certain countries where leniolisib is not commercially available.
European Economic Area (EEA)
As part of the review process of the Marketing Authorisation Application (MAA) for leniolisib for patients 12 years of age and older, Pharming submitted its response to the European Medicines Agency’s (EMA) Committee for Human Medicinal Products (CHMP) Day 180 list of outstanding issues (LoOI) in October 2023. In November 2023, Pharming received a Day 180 Second LoOI from the CHMP. The CHMP consulted an Ad-Hoc Expert Group (AEG) at a meeting held at the end of November. Pharming is working closely with the CHMP to address the remaining outstanding issues and we are now awaiting CHMP’s opinion on the leniolisib MAA.
United Kingdom
In November 2023, Pharming announced its intention to file an MAA with the U.K. Medicines and Healthcare products Regulatory Agency (MHRA) through the International Recognition Procedure (IRP) which replaced the European Commission Decision Recognition Procedure (ECDRP) from January 1, 2024. Pharming submitted an MAA for leniolisib on the basis of the US FDA approval on March 12, 2024.
Japan clinical trial
In May 2023, leniolisib was granted orphan drug designation (ODD) by the Ministry of Health, Labour and Welfare of Japan (MHLW) for the treatment of APDS. In August 2023, Pharming announced that the first patient was enrolled in a Phase III clinical trial in Japan evaluating leniolisib for the treatment of APDS in adult and pediatric patients 12 years of age and older. Patient enrollment in this study is now complete.
The single-arm, open-label clinical trial will evaluate the safety, tolerability, and efficacy of leniolisib in three patients, 12 years of age and older, who have a confirmed APDS diagnosis. The study’s primary efficacy endpoints and secondary endpoints mirror those used to evaluate the clinical outcomes of the earlier leniolisib APDS trials.
Pharming plans to file an application for the approval of leniolisib with Japan’s Pharmaceuticals and Medical Devices Agency (PMDA), following completion of the appropriate clinical trials. An approval decision would be expected in nine months based on priority review of the application due to ODD. Eligible patients enrolled in the trial will continue to receive the investigational drug for at least an additional year through an open-label extension trial.
Additional markets
Pharming filed regulatory submissions in Canada and Australia in the third quarter of 2023, and Israel in the second quarter. These submissions are progressing as expected and we anticipate regulatory action in 2024 for Canada, Australia, and Israel.
Pediatric clinical trials
In 2023, Pharming initiated two pediatric clinical trials, for children ages 4 to 11 and ages 1 to 6 years old, at sites in the U.S., Japan, and the EU. The single-arm, open-label, multinational clinical trials will evaluate the safety, tolerability, and efficacy of leniolisib in 15 children, per clinical trial, who have a confirmed APDS diagnosis. The primary efficacy endpoints and secondary endpoints of the studies mirror those used to evaluate the clinical outcomes in the previous leniolisib Phase II/III APDS trials for patients aged 12 and older.
Pharming is nearing completion of enrollment in the clinical trial for children ages 4 to 11 years old.
In November 2023, the first patient was dosed in the clinical trial for children ages 1 to 6 years old. Enrollment in the study is continuing as planned.
Leniolisib for additional indications (PI3Kδ platform) - Primary immunodeficiencies (PIDs) beyond APDS
As we continue to work towards regulatory approvals of leniolisib for APDS in additional geographies and pediatric label expansion, we have also commenced work to identify and prioritize other indications where leniolisib has the potential to deliver value for patients. PI3Kδ has been identified as an important player in a variety of disease states, and leniolisib has demonstrated an attractive, long-term efficacy, safety and tolerability profile in clinical trials conducted in both healthy volunteers and APDS patients. This provides a solid basis for our plans for the investigation and investment in further leniolisib indications.
In December 2023, Pharming announced the expansion of its rare disease pipeline with plans to develop leniolisib for additional primary immunodeficiencies (PIDs) with greater prevalence than APDS. Pharming has engaged with and received feedback from the US FDA on its plans to develop leniolisib for PID disorders with immune dysregulation.
Primary immunodeficiencies (PIDs) with immune dysregulation
Leniolisib, by reducing PI3Kδ activity, could help rebalance immune dysregulation in PIDs, positively impacting clinical manifestations including lymphoproliferation and autoimmunity. Pharming is now in the final stages of preparation for the start of an initial Phase 2, proof of concept, clinical trial in targeted PID genetic disorders with immune dysregulation linked to PI3Kẟ signaling in lymphocytes, with similar clinical phenotypes and unmet medical need to APDS. These PID disorders include ALPS-FAS, CTLA4 haploinsufficiency and PTEN deficiency. The epidemiology of these targeted PID genetic disorders suggests a prevalence of approximately five patients per million.
The Phase 2 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 this new PID population. The trial has been designed to inform a subsequent Phase 3 program.
Organizational highlights
During 2023 our new Chairman, Dr. Richard Peters, was elected, succeeding Paul Sekhri, who came to the end of his maximum term (eight years). Dr. Peters is a highly respected and proven industry leader, who brings extensive medical and commercial acumen for difficult-to-treat and rare diseases, from development stage to large global biopharmaceutical companies, to Pharming. We also strengthened our Executive Committee with the appointment of a Chief Business Officer, Dr. Alexander Breidenbach, who has more than 20 years of partnering, R&D and management experience in biosciences and, in this newly created position, is tasked with the development and execution of Pharming’s growth strategy.
Financial Summary
| Amounts in US$m except per share data | 4Q 2023 | 4Q 2022 | 2023 | 2022 |
| Consolidated Statement of Income | ||||
| Revenue - RUCONEST® | 73.3 | 54.6 | 227.1 | 205.6 |
| Revenue - Joenja® | 7.9 | 0.0 | 18.2 | 0.0 |
| Total Revenues | 81.2 | 54.6 | 245.3 | 205.6 |
| Cost of sales | (7.1) | (6.3) | (25.2) | (17.6) |
| Gross profit | 74.1 | 48.3 | 220.1 | 188.1 |
| Other income | 0.5 | (1.1) | 23.3 | 14.5 |
| Research and development | (11.6) | (10.9) | (68.9) | (52.5) |
| General and administrative | (24.0) | (17.6) | (55.9) | (46.0) |
| Marketing and sales | (37.9) | (29.0) | (124.0) | (85.8) |
| Operating profit (loss) | 1.1 | (10.2) | (5.4) | 18.2 |
| Fair value gain (loss) on revaluation | (0.9) | (1.2) | (0.9) | (1.2) |
| Other finance income | 1.6 | (4.8) | 3.7 | 4.5 |
| Other finance expenses | (4.5) | (1.5) | (9.1) | (5.5) |
| Share of net profits in associates using the equity method | 0.7 | (0.4) | (0.3) | (1.1) |
| Profit (loss) before tax | (2.0) | (18.1) | (12.0) | 15.0 |
| Income tax credit (expense) | (0.7) | 3.5 | 1.9 | (1.3) |
| Profit (loss) for the period | (2.7) | (14.6) | (10.1) | 13.7 |
| Share Information | ||||
| Basic earnings per share (US$) | (0.004) | (0.022) | (0.015) | 0.021 |
| Diluted earnings per share (US$) | (0.004) | (0.022) | (0.015) | 0.019 |
| Amounts in US$m | December 31, 2023 | December 31, 2022 |
| Balance Sheet | ||
| Cash and cash equivalents, restricted cash and marketable securities | 215.0 | 208.7 |
| Current assets | 316.3 | 277.5 |
| Total assets | 461.4 | 425.8 |
| Current liabilities | 76.1 | 59.7 |
| Equity | 219.2 | 204.6 |
Financial highlights
Fourth quarter 2023
Revenues in the fourth quarter of 2023 increased to US
Gross profit in the fourth quarter of 2023 increased by US
Operating expenses increased by US
In the fourth quarter of 2023, an operating profit of US
Full year 2023
In 2023, Pharming revenues increased by
This section will further elaborate on Pharming's financial performance in 2023.
Revenues and Gross Profit
The
Cost of sales increased by
Gross profit increased by US
Operating Profit (loss) and Other Operating Costs
For 2023, operating profit (loss) decreased by US
Of the US
In 2023, other income increased by US
Finance income and expenses
Other finance income decreased by US
Other finance expenses increased by US
The fair value loss on revaluation (US
Income tax credit (expense)
Income tax credit (expense) shifted from a US
Profit (loss) for the year
The total net loss in 2023 amounted to US
Intangible assets
In 2023, intangible assets decreased by US
The amortization relates to regular amortization of software and the existing re-acquired rights related to the acquisition of all North American commercialization rights from Bausch Health in 2016 and the acquisition of all European commercialization and distribution rights from Swedish Orphan International AB (“Sobi”) in 2020. In addition to the aforementioned, the amortization of the Joenja® license commenced, following the FDA approval per March 24, 2023. Amortization is charged based on the economic lifetime of the intangible asset. The economic lifetime of the North American commercialization rights from Bausch Health is 20 years, where the economic lifetime of the European commercialization and distribution rights from Swedish Orphan International AB is 12 years. These estimates did not change compared to the previous year. The economic lifetime of the Joenja® license is established at 14 years.
Property, plant and equipment
The value of property, plant and equipment decreased from US
Right-of-use assets
The right-of-use assets decreased from US
The decrease in the right-to-use assets is partially offset by investments in buildings (US
Investments
Investments increased by US
The increase in investments was partially offset by Pharming’s share of US
Inventories
Inventories increased from US
Cash and cash equivalents and marketable securities
Cash and cash equivalents alone decreased by US
In 2023, the Company invested in euro-denominated readily convertible S&P AAA-rated government treasury certificates with a maturity of six months or less from the date of acquisition. As of year-end 2023, these marketable securities amount to US
The combined total of cash and cash equivalents, together with restricted cash and marketable securities increased from US
Equity
The equity position increased by US
Convertible bond
The convertible bond has increased by US
Lease liabilities
Lease liabilities decreased by US
Outlook/Summary
For 2024, the Company anticipates:
- Total revenues between US
$280 million and US$295 million (14% to20% growth), with quarterly fluctuations expected. - 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 ex-U.S. revenues leniolisib - from commercial availability or 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, the U.K., Canada, Australia, and Israel.
- Initiate and advance a Phase 2 clinical trial for leniolisib in PIDs with immune dysregulation linked to PI3Kδ signaling to significantly expand the long-term commercial potential of leniolisib.
- Continued operating cost investments to accelerate future revenue growth. Our current cash on hand and the continued cash flow from product revenues are expected to be sufficient to fund these investments. No material cash burn is expected prior to the impact of potential acquisition or in-licensing transactions.
- 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 CET today.
Conference Call
The conference call will begin at 13:30 CET/08:30 am EDT on Thursday, March 14. 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/5wi4ajdm
Conference call dial-in details:
https://register.vevent.com/register/BIc993931aa2d54aa89d594b2cad5ed972
Additional information on how to register for the conference call/webcast can be found on the
Pharming.com website.
Financial Calendar 2024
Annual Report and 20-F 2023 April 4
1Q 2024 financial results May 8
Annual General Meeting of Shareholders May 21
2Q/1H 2024 financial results August 1
3Q 2024 financial results October 24
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, biologics, and gene therapies that are in early to late-stage development. Pharming is headquartered in Leiden, 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.
Risk profile
We continue to closely monitor and manage the key risks and opportunities, and will respond appropriately to any emerging risk. We will issue a full overview of our risk profile in our Annual report 2023 to be published on April 4, 2024.
Related party transactions
There are no material changes in the nature, scope, and (relative) scale in this reporting period compared to last year.
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 and technical developments. In light of these risks and uncertainties, and other risks and uncertainties that are described in Pharming's 2022 Annual Report and the Annual Report on Form 20-F for the year ended December 31, 2022, 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 Financial Statements in U.S. Dollars (unaudited)
For the year ended 31 December 2023
- Condensed consolidated statement of income
- Condensed consolidated statement of comprehensive income
- Condensed consolidated balance sheet
- Condensed consolidated statement of changes in equity
- Condensed consolidated statement of cash flow
| CONDENSED CONSOLIDATED STATEMENT OF INCOME | ||
| For the year ended 31 December | ||
| Amounts in US$ ‘000 | 2023 | 2022 |
| Revenues | 245,316 | 205,622 |
| Costs of sales | (25,212) | (17,562) |
| Gross profit | 220,104 | 188,060 |
| Other income | 23,349 | 14,523 |
| Research and development | (68,914) | (52,531) |
| General and administrative | (55,877) | (46,016) |
| Marketing and sales | (124,049) | (85,803) |
| Other Operating Costs | (248,840) | (184,350) |
| Operating profit (loss) | (5,387) | 18,233 |
| Fair value gain (loss) on revaluation | (930) | (1,185) |
| Other finance income | 3,663 | 4,485 |
| Other finance expenses | (9,069) | (5,463) |
| Finance result, net | (6,336) | (2,163) |
| Share of net profits (loss) in associates using the equity method | (289) | (1,083) |
| Profit (loss) before tax | (12,012) | 14,987 |
| Income tax expense | 1,893 | (1,313) |
| Profit (loss) for the year | (10,119) | 13,674 |
| Basic earnings per share (US$) | (0.015) | 0.021 |
| Diluted earnings per share (US$) | (0.015) | 0.019 |
| CONDENSED CONSOLIDATED STATEMENT OF COMPREHENSIVE INCOME | ||
| For the year ended 31 December | ||
| Amounts in US$ ‘000 | 2023 | 2022 |
| Profit (loss) for the year | (10,119) | 13,674 |
| Currency translation differences | 5,913 | (10,349) |
| Items that may be subsequently reclassified to profit or loss | 5,913 | (10,349) |
| Fair value remeasurement investments | 1,167 | (705) |
| Items that shall not be subsequently reclassified to profit or loss | 1,167 | (705) |
| Other comprehensive income (loss), net of tax | 7,080 | (11,054) |
| Total comprehensive income (loss) for the year | (3,039) | 2,620 |
| CONDENSED CONSOLIDATED BALANCE SHEET | ||
| As at 31 December | ||
| Amounts in US$ ‘000 | 2023 | 2022 |
| Non-current assets | ||
| Intangible assets | 71,267 | 75,121 |
| Property, plant and equipment | 9,689 | 10,392 |
| Right-of-use assets | 23,777 | 28,753 |
| Long-term prepayments | 92 | 228 |
| Deferred tax assets | 28,332 | 22,973 |
| Investment accounted for using the equity method | 2,285 | 2,501 |
| Investments in equity instruments designated as at FVTOCI | 2,020 | 403 |
| Investment in debt instruments designated as at FVTPL | 6,093 | 6,827 |
| Restricted cash | 1,528 | 1,099 |
| Total non-current assets | 145,083 | 148,297 |
| Current assets | ||
| Inventories | 56,760 | 42,326 |
| Trade and other receivables | 46,157 | 27,619 |
| Restricted cash | 222 | 213 |
| Marketable securities | 151,683 | — |
| Cash and cash equivalents | 61,519 | 207,342 |
| Total current assets | 316,341 | 277,500 |
| Total assets | 461,424 | 425,797 |
| Share capital | 7,669 | 7,509 |
| Share premium | 478,431 | 462,297 |
| Other reserves | (2,080) | (8,737) |
| Accumulated deficit | (264,834) | (256,431) |
| Shareholders’ equity | 219,186 | 204,638 |
| Non-current liabilities | ||
| Convertible bonds | 136,598 | 131,618 |
| Lease liabilities | 29,507 | 29,843 |
| Total non-current liabilities | 166,105 | 161,461 |
| Current liabilities | ||
| Convertible bonds | 1,824 | 1,768 |
| Trade and other payables | 70,693 | 54,465 |
| Lease liabilities | 3,616 | 3,465 |
| Total current liabilities | 76,133 | 59,698 |
| Total equity and liabilities | 461,424 | 425,797 |
| CONDENSED CONSOLIDATED STATEMENT CHANGES IN EQUITY | ||
| For the period ended 31 December | ||
| Attributable to owners of the parent | ||
| Amounts in US$ ‘000 | Share capital | Share premium | Other reserves | Accumulated deficit | Total equity |
| Balance at January 1, 2022 | 7,429 | 455,254 | 3,400 | (273,167) | 192,916 |
| Profit (loss) for the year | — | — | — | 13,674 | 13,674 |
| Other comprehensive income (loss) for the year | — | — | (11,054) | — | (11,054) |
| Total comprehensive income (loss) for the year | — | — | (11,054) | 13,674 | 2,620 |
| Other reserves | — | — | (1,083) | 1,083 | — |
| Income tax benefit from excess tax deductions related to share-based payments | — | — | — | 430 | 430 |
| Share-based compensation | — | — | — | 6,392 | 6,392 |
| Options exercised / LTIP shares issued | 80 | 7,043 | — | (4,843) | 2,280 |
| Total transactions with owners, recognized directly in equity | 80 | 7,043 | (1,083) | 3,062 | 9,102 |
| Balance at December 31, 2022 | 7,509 | 462,297 | (8,737) | (256,431) | 204,638 |
| Profit (loss) for the year | — | — | — | (10,119) | (10,119) |
| Other comprehensive income (loss) for the year | — | — | 7,080 | — | 7,080 |
| Total comprehensive income (loss) for the year | — | — | 7,080 | (10,119) | (3,039) |
| Other reserves | — | — | (423) | 423 | — |
| Income tax benefit from excess tax deductions related to share-based payments | — | — | — | 203 | 203 |
| Share-based compensation | — | — | — | 9,251 | 9,251 |
| Options exercised / LTIP shares issued | 160 | 16,134 | — | (8,161) | 8,133 |
| Total transactions with owners, recognized directly in equity | 160 | 16,134 | (423) | 1,716 | 17,587 |
| Balance at December 31, 2023 | 7,669 | 478,431 | (2,080) | (264,834) | 219,186 |
| CONDENSED CONSOLIDATED STATEMENT OF CASH FLOWS | |||
| For the year ended 31 December | |||
| Amounts in $’000 | 2023 | 2022 | |
| Profit (loss) before tax | (12,012) | 14,987 | |
| Adjustments to reconcile net profit (loss) to net cash used in operating activities: | |||
| Depreciation, amortization, impairment of non-current assets | 15,925 | 13,188 | |
| Equity settled share based payments | 9,251 | 6,392 | |
| Gain on disposal of investment in associate | 0 | (12,242) | |
| Fair value gain (loss) on revaluation | 930 | 1,185 | |
| Gain on disposal from PRV sale | (21,279) | 0 | |
| Other finance income | (3,663) | (4,485) | |
| Other finance expenses | 9,069 | 5,463 | |
| Share of net profits in associates using the equity method | 289 | 1,083 | |
| Other | (1,080) | (1,576) | |
| Operating cash flows before changes in working capital | (2,570) | 23,995 | |
| Changes in working capital: | |||
| Inventories | (14,434) | (15,016) | |
| Trade and other receivables | (18,538) | 2,364 | |
| Payables and other current liabilities | 16,228 | 11,992 | |
| Restricted cash | (438) | 273 | |
| Total changes in working capital | (17,182) | (387) | |
| Interest received (paid) | 2,883 | 85 | |
| Income taxes received (paid) | (655) | (1,235) | |
| Net cash flows generated from (used in) operating activities | (17,524) | 22,458 | |
| Capital expenditure for property, plant and equipment | (1,437) | (1,376) | |
| Proceeds on PRV sale | 21,279 | 0 | |
| Investment intangible assets | (27) | (601) | |
| Proceed from sale of Investment associate | 0 | 7,300 | |
| Purchases of marketable securities | (382,014) | 0 | |
| Proceeds from sale of marketable securities | 232,811 | 0 | |
| Net cash flows generated from (used in) investing activities | (129,388) | 5,323 | |
| Payment of lease liabilities | (5,126) | (3,311) | |
| Interests on loans and leases | (4,046) | (3,952) | |
| Settlement of share based compensation awards | 8,133 | 2,281 | |
| Net cash flows generated from (used in) financing activities | (1,039) | (4,982) | |
| Increase (decrease) of cash | (147,951) | 22,799 | |
| Exchange rate effects | 2,128 | (7,381) | |
| Cash and cash equivalents at January 1 | 207,342 | 191,924 | |
| Total cash and cash equivalents at December 31 | 61,519 | 207,342 |
---ENDS---
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