Pharming Group N.V.

Earnings Release • Jul 30, 2020

Pharming Group reports financial results for the first half of 2020

Delivered 14% increase in revenue, 31% increase in operating profit and 33% increase in net profit year-on-year

Leiden, The Netherlands, 30 July 2020: Pharming Group N.V. ("Pharming" or "the Company") (Euronext Amsterdam: PHARM) presents its (unaudited) financial report for the six months ended 30 June 2020.

The Company will hold a conference call at 13:00 CEST / 07:00 EST today. Dial-in details can be found on page 6 of this report.

Financial summary

	H1 2020	H1 2019	% Change
Amounts in €m except per share data
Income Statement
Revenues	88.6	77.9	14%
Gross profit	78.7	67.0	17%
Operating result	32.3	24.6	31%
Net result	18.1	13.6	33%
Balance Sheet
Cash & marketable securities	155.1	65.3	138%
Share Information
Earnings per share (€):
Undiluted -	0.029	0.022	32%
Fully diluted -	0.025	0.020	25%

Six months to 30 June 2020

Financial highlights

• The Company achieved record revenues in H1 2020, with a 14% increase year-on-year to €88.6 million (H1 2019: €77.9 million).
• US revenues increased 13% year-on-year to €85.0 million (H1 2019: €75.0 million), however, sales in Q2 2020 declined by 21% compared to Q1 2020. This was as a result of an unusually high sales level towards the end of Q1 2020, which is believed to have included some pre-filling of prescriptions in response to the emerging COVID-19 pandemic. The Company therefore believes that the H1 2020 results are more representative of underlying performance, than either quarter in isolation.
• In Europe and the rest of the world (RoW), revenues for H1 2020 increased 24% year-on-year to €3.6 million (H1 2019: €2.9 million), as a result of significant growth in the EU. This follows the reacquisition of commercial product rights in EU territories, effective from 1 January 2020, as well as volume increases in the EU.
• Operating profit in H1 2020 increased 31% year-on-year to €32.3 million (H1 2019: €24.6 million).

• Net profits in H1 2020 increased 33% year-on-year to €18.1 million (H1 2019: €13.6 million). Despite the decrease in US sales in Q2 2020, net profit for the quarter increased to €9.7 million from €8.4 million in Q1 2020, mainly as a result of lower financing costs following the successful convertible bond refinancing in January 2020 and continued cost control.

• Strengthened cash position to €155.1 million as of 30 June 2020, an increase of €19 million from €136.1 million at 31 March 2020 (cash at 31 December of €68.6 million). This is a result of strong positive operational cashflows during both Q1 and Q2, from Q2 onwards also supported by lower financing costs as result of the successful convertible bond re-financing in Q1.

• The equity position improved from €104.7 million at the end of December 2019 to €127.6 million at the end of June 2020. The majority of the increase in equity is related to the net result for the first half.
• Other financial liabilities, which refers to the contingent consideration reserved for the final successful sales performance milestone of US\$25 million to Bausch Health, did not increase. As a result, our estimation of the likelihood of paying this milestone in the future has not changed during the period.
• Since the last reporting date of 20 May 2020, the Company has issued, or reserved for issue, a total of 2.748.244 shares in connection with a number of exercises of options under the current schemes. The number of issued shares as of 30 July 2020 is 637.743.008. The fully diluted number of shares as of 30 July 2020 is 740.943.581.

Operational highlights

• On 14 January 2020, the Company announced the placement of a €125 million 3% senior unsecured convertible bonds due 2025. The proceeds of the issue were used to redeem the remaining \$56 million of the original \$100 million loan from Orbimed Advisors and therefore reduced the Company's financing costs. The remaining balance of the net proceeds will support the Company's capital expenditure in relation to the expansion of commercialisation and manufacturing infrastructure.
• During Q1 2020, Pharming received European and US validation of its new production facility of starting material for the Company's lead product, RUCONEST®. On 21 January 2020, the Company received European Medicines Agency (EMA) approval for a Type II Variation for the new production facility. On 9 March 2020, the Company received approval on its Prior Approval Supplement from the US Food and Drug Administration (FDA) for the new production facility.
• On 11 March 2020, the Company announced Chief Financial Officer (CFO), Robin Wright, would not put himself up for re-election as a member of the Board of Management and therefore as CFO at the General Meeting of Shareholders. As a result, Robin Wright's term with Pharming ended on 20 May 2020. The search for a new CFO is well underway.
• On 23 March 2020, the Company announced it had been promoted to the Euronext Amsterdam MidKap index (AMX).
• On 21 April 2020, the Company reported encouraging results from a study of five patients with confirmed COVID-19 (SARS-CoV-2) infections hospitalised with related severe pneumonia that were treated with RUCONEST® under a compassionate use programme at the University Hospital of Basel, Switzerland. Following these encouraging results, a multinational, randomised, controlled investigator-initiated study, led by Dr Michael Osthoff from the University Hospital of Basel, is ready to recruit patients. Pharming expects the study to include up to 150 patients and to be carried out in multiple research centres in parallel, in Switzerland, the US and Latin-America.
• On 30 April 2020, the Company announced that the European Commission had approved an extension in the indication of RUCONEST®'s Marketing Authorisation to include the treatment

of acute hereditary angioedema (HAE) attacks in children (aged 2-13). In the EU, RUCONEST® has been approved for the treatment of acute HAE attacks in adults since 2010 and in adolescents since 2016.

• On 20 May 2020, the Company announced the nomination of Barbara Yanni and Mark Pyktett to the Board of Supervisory Directors. An Extraordinary General Meeting of Shareholders (EGM) is expected to convene in Q4 2020 for their official appointments. Until that time, both Barbara and Mark will hold observational roles.

COVID-19 update

Pharming continues to comply with international guidance and requirements across its operations to prioritise the health and safety of its employees during the COVID-19 pandemic.

An update on the impact of COVID-19 on the operations of the business is summarised below.

• No impact on the upscaling or continued production of RUCONEST®. The Company's new starting material facility, approved earlier this year, significantly increases Pharming's production capacity of RUCONEST®.
• No impact on the availability or distribution of RUCONEST® to HAE patients.
• The recruitment of new patients in ongoing clinical trials has been temporarily halted; patients already incorporated into ongoing clinical trials will continue to receive treatment.
• As a result of halted recruitment, timelines for the pre-eclampsia and acute kidney injury studies are expected to incur delays, subject to the return of recruitment.
• Recruitment in the registration enabling trial for leniolisib has started again and we continue to expect the potential launch of leniolisib in mid-2022.

Sijmen de Vries, Chief Executive Officer, commented:

"We are delighted to announce strong results for the first half of the year, demonstrating consistent progress in a challenging period that included the restriction of all face-to-face sales and marketing activities. Thanks to the dedication, creativity and tenacity of our employees, we have been able to continue our growth trajectory, both in terms of production capacity and sales expansion, to deliver record results. We also continued to increase net profitability, supported by our successful convertible bond refinancing, which significantly lowered our financing costs, and the re-acquisition of RUCONEST®'s commercialisation rights for the remaining EU territories.

In addition, we have continued to demonstrate operational success, receiving EMA and FDA approval for a new production facility of RUCONEST® starting material, receiving approval for an expansion of the EU Marketing Authorisation for RUCONEST® to include children aged 2-13, and reporting encouraging results from a compassionate use study in the treatment of severe pneumonia related to COVID-19 with RUCONEST®, a further investigation into which is due to begin shortly. We are also encouraged that recruitment in the pivotal study for leniolisib has started again and we continue to expect the potential launch of the product in mid-2022. We remain confident we are well positioned to continue to deliver significant value to all our stakeholders in the second half of the year and beyond."

Outlook

For the remainder of 2020, the Company expects:

• Subject to progression of the COVID-19 pandemic in the US; continued growth in revenues from sales of RUCONEST®, compared to the first half of 2020, mainly driven by the US and expanded European operations.
• Maintenance of positive net earnings during the year.
• Continued investment in the expansion of production of RUCONEST® in order to ensure continuity of supply to the growing markets in the US, Europe, China and the RoW.
• Investment in the ongoing clinical trials for pre-eclampsia and acute kidney injury, and support for investigators wishing to explore additional indications for RUCONEST®, such as the planned study in patients confirmed with COVID-19 infections with related severe pneumonia.
• Initiation of patient recruitment of the investigator sponsored, randomised controlled COVID-19 study, in centres in Switzerland, USA and Latin America.
• Investment in the continuing registration-enabling study for leniolisib for APDS, leading to headline data early in 2021.
• Investment in an Investigational New Drug Application to the FDA enabling studies for αglucosidase in Pompe disease and preclinical development of the new recombinant αgalactosidase candidate for Fabry's disease.
• Investment in acquisitions / in-licensing of other new development opportunities and assets as these occur.
• Increasing marketing activity where this can be profit-enhancing for Pharming.
• Continued close monitoring of the ongoing COVID-19 pandemic and the potential impact on the business.

No further financial guidance for 2020 is provided.

Statement of the Board of Management

The Board of Management declares that to the best of its knowledge and in accordance with applicable reporting principles, the half-year consolidated financial statements give a true and fair view of the assets, liabilities, financial position and profit or loss of Pharming, and the half-year report incorporated in this press release includes a fair review of the development and performance of the business and the position of the Company, together with additional information on certain risks associated with the expected development of the Company.

Board of Management:

Sijmen de Vries, CEO

Bruno Giannetti, COO

About Pharming Group N.V.

Pharming is a specialty pharmaceutical company developing innovative products for the safe, effective treatment of rare diseases and unmet medical needs. Pharming's lead product, RUCONEST® (conestat alfa) is a recombinant human C1 esterase inhibitor approved for the treatment of acute Hereditary Angioedema ("HAE") attacks in patients in Europe, the US, Israel and South Korea. The product is

available on a named-patient basis in other territories where it has not yet obtained marketing authorisation.

RUCONEST® is commercialised by Pharming in the US and in Europe, and the Company holds all other commercialisation rights in other countries not specified below. In some of these other countries distribution is made in association with the HAEi Global Access Program (GAP). RUCONEST® is distributed in Argentina, Colombia, Costa Rica, the Dominican Republic, Panama, and Venezuela by Cytobioteck, in South Korea by HyupJin Corporation and in Israel by Kamada.

RUCONEST® is also being evaluated for various additional indications. Pharming's technology platform includes a unique production process that has proven capable of producing industrial quantities of pure high quality recombinant human proteins in a more economical and less immunogenic way compared with current cell-line based methods.

Leads for enzyme replacement therapy ("ERT") for Pompe and Fabry's diseases are also being produced and optimised respectively at present.

Pharming has recently in-licensed leniolisib from Novartis, a small molecule and selective PI3Kδ inhibitor, which is in a registrational study for activated PI3K-delta syndrome (APDS), a rare form of Primary Immunodeficiency.

Pharming has a long term partnership with the China State Institute of Pharmaceutical Industry ("CSIPI"), a Sinopharm company, for joint global development of new products, starting with recombinant human Factor VIII for the treatment of Haemophilia A. Preclinical development and manufacturing will take place to global standards at CSIPI and its affiliates and are funded by CSIPI. Clinical development will be shared between the partners with each partner taking the costs for their territories under the partnership.

Additional information is available on the Pharming website: www.pharming.com

Forward-looking Statements

This press release of Pharming Group N.V. and its subsidiaries ("Pharming", the "Company" or the "Group") may contain forward-looking statements including without limitation those regarding Pharming's financial projections, market expectations, developments, partnerships, plans, strategies and capital expenditures.

The Company cautions that such forward-looking statements may involve certain risks and uncertainties, and actual results may differ. Risks and uncertainties include without limitation the effect of competitive, political and economic factors, legal claims, the Company's ability to protect intellectual property, fluctuations in exchange and interest rates, changes in taxation laws or rates, changes in legislation or accountancy practices and the Company's ability to identify, develop and successfully commercialize new products, markets or technologies.

As a result, the Company's actual performance, position and financial results and statements may differ materially from the plans, goals and expectations set forth in such forward-looking statements. The Company assumes no obligation to update any forward-looking statements or information, which should be taken as of their respective dates of issue, unless required by laws or regulations.

For further public information, contact:

Pharming Group N.V.

Sijmen de Vries, CEO, Tel: +31 71 524 7400

Susanne Embleton, Investor Relations Manager: +31 71 524 7400

FTI Consulting, London, UK:

Victoria Foster Mitchell, Tel: +44 203 727 1136

LifeSpring Life Sciences Communication, Amsterdam, The Netherlands:

Leon Melens, Tel: +31 6 53 81 64 27

Conference call information

From the Netherlands:	+31 207095189
	Toll-Free: 08004050000
From the UK:	+44 3333000804
	Toll-Free: 08003589473
From Belgium:	+32 24035814
	Toll-Free: 080029913
From France:	+33 170750711
	Toll-Free: 0800946608
From Switzerland:	+41 225809034
	Toll-Free: 0800721298
From the US:	+1 6319131422
	Toll-Free: +1 855 85 70686

For other numbers, please see: https://events-ftp.arkadin.com/ev/docs/NE\_W2\_TF\_Events\_International\_Access\_List.pdf

Presentation link:

https://arkadin-event.webex.com/arkadinevent/onstage/g.php?MTID=e46000d81240a97b2024e3fa98526bd10

Presentation Password/PIN: 31591389

Pharming Group N.V.

Condensed Consolidated Interim Financial Statements (unaudited)

For the period ended 30 June 2020

• Condensed consolidated statement of profit or loss
• Condensed consolidated statement of comprehensive income
• Condensed consolidated statement of financial position
• Condensed consolidated statement of changes in equity
• Condensed consolidated statement of cash flow

Notes to the condensed consolidated interim financial statements

Appendix: Main Condensed Consolidated Interim Financial Statements reported in US dollars

(This appendix is not part of the Condensed Consolidated Interim Financial Statements)

• Condensed consolidated statement of profit or loss in US Dollar
• Condensed consolidated statement of financial position in US Dollar
• Condensed consolidated statement of cash flows in US Dollar

Condensed Consolidated Statement of Profit or Loss For the period ended 30 June

Amounts in € '000	notes	HY 2020	HY 2019
Revenues	7	88.593	77.935
Costs of sales	8	(9.858)	(10.956)
Gross profit		78.735	66.979
Other income		475	148
Research and development		(15.991)	(14.877)
General and administrative		(8.917)	(6.842)
Marketing and sales		(21.991)	(20.776)
Costs	8	(46.899)	(42.495)
Operating result		32.311	24.632
Fair value gain (loss) on revaluation derivatives		84	(8)
Other financial income	9	1.121	506
Other financial expenses	9	(7.741)	(6.767)
Financial income and expenses		(6.536)	(6.269)
Share of net profits in associates using the equity method	10	121	299
Result before income tax		25.896	18.662
Income tax credit (expense)		(7.753)	(5.068)
Net result for the year		18.143	13.594
Attributable to:
Owners of the parent		18.143	13.594
Total net result		18.143	13.594
Basic earnings per share (€)	15	0,029	0,022
Fully-diluted earnings per share (€)	15	0,025	0,020

Condensed Consolidated Statement of Comprehensive Income For the period ended 30 June

Amounts in € '000	HY 2020	HY 2019
Net result for the year	18.143	13.594
Currency translation differences	35	(200)
Items that may be subsequently reclassified to profit or loss	35	(200)
Other comprehensive income (loss), net of tax	35	(200)
Total comprehensive income (loss) for the year	18.178	13.394
Attributable to:
Owners of the parent	18.178	13.394

Condensed Consolidated Balance Sheet As at date shown

Amounts in € '000	notes	30 June 2020	31 December 2019
Intangible assets	16	77.219	70.809
Property, plant and equipment		8.748	8.553
Right-of-use assets		5.284	5.979
Deferred tax assets	17	22.582	28.590
Investments accounted for using the equity method	10	5.616	5.508
Restricted cash		2.272	2.268
Non-current assets		121.721	121.707
Inventories	11	16.223	14.467
Trade and other receivables		26.386	25.737
Cash and cash equivalents		152.782	66.299
Current assets		195.391	106.503
Total assets		317.112	228.210
Share capital		6.377	6.313
Share premium		396.033	392.266
Legal reserves		3.809	3.718
Accumulated deficit		(278.650)	(297.618)
Shareholders' equity	12	127.569	104.679
Convertible bonds	13	123.222	-
Lease liabilities	14	4.133	4.363
Other financial liabilities		18.298	17.282
Non-current liabilities		145.653	21.645
Loans and borrowings	13	-	45.590
Derivative financial liabilities		185	268
Trade and other payables		42.158	36.247
Lease liabilities		1.547	1.946
Other financial liabilities		-	17.835
Current liabilities		43.890	101.886
Total equity and liabilities		317.112	228.210

Condensed Consolidated Statement of Changes in Equity For the period ended 30 June

Attributable to owners of the parent

Amounts in € '000	notes	Number of shares (in '000)	Share capital	Share premium
Balance at 1 January 2019 as reported in HY report		621.501	6.215	387.525
Result for the year		-	-	-
Other comprehensive income (loss) for the half-year		-	-	-
Total comprehensive income (loss) for the half-year		-	-	-
Legal reserves development expenses		-	-	-
Share-based compensation		-	-	-
Bonuses settled in shares		3	-	3
Shares issued for cash		1.635	16	228
Warrants exercised/ issued		180	1	158
Options exercised		2.564	25	1.396
Total transactions with owners, recognised directly in equity		4.382	42	1.785
Balance at 30 June 2019		625.883	6.257	389.310

Balance at 1 January 2020		631.323	6.313	392.266
Result for the half-year		-	-	-
Other comprehensive income (loss) for the half-year		-	-	-
Total comprehensive income (loss) for the half-year		-	-	-
Legal reserves development expenses		-	-	-
Share-based compensation		-	-	-
Bonuses settled in shares	12	-	-	-
Value of conversion rights on convertible bonds	14	-	-	-
Shares issued for cash	12	2.061	21	1.389
Warrants exercised/ issued	12	-	-	-
Options exercised	12	4.319	43	2.378
Total transactions with owners, recognised directly in equity		6.380	64	3.767
Balance at 30 June 2020		637.703	6.377	396.033

The notes are an integral part of these interim financial statements

Attributable to owners of the parent

Amounts in € '000	notes	Legal reserves		Accumulated deficit	Total equity
		Capitalized development cost	Translation reserve
Balance at 1 January 2019 as reported in HY report		2.237	(590)	(333.636)	61.751
Result for the year		-	-	13.594	13.594
Other comprehensive income (loss) for the half-year		-	(200)	-	(200)
Total comprehensive income (loss) for the half-year		-	(200)	13.594	13.394
Legal reserves development expenses		310	-	(310)	-
Share-based compensation		-	-	1.350	1.350
Bonuses settled in shares		-	-	-	3
Shares issued for cash		-	-	(244)	-
Warrants exercised/ issued		-	-	-	159
Options exercised		-	-	(588)	833
Total transactions with owners, recognised directly in equity		310	-	208	2.345
Balance at 30 June 2019		2.547	(790)	(319.834)	77.490

Balance at 1 January 2020		4.347	(629)	(297.618)	104.679
Result for the half-year		-	-	18.143	18.143
Other comprehensive income (loss) for the half-year		-	35	-	35
Total comprehensive income (loss) for the half-year		-	35	18.143	18.178
Legal reserves development expenses		56	-	(56)	-
Share-based compensation		-	-	1.391	1.391
Bonuses settled in shares	12	-	-	-	-
Value of conversion rights on convertible bonds	14	-	-	1.405	1.405
Shares issued for cash	12	-	-	(1.410)	-
Warrants exercised/ issued	12	-	-	-	-
Options exercised	12	-	-	(505)	1.916
Total transactions with owners, recognised directly in equity		56	-	825	4.712
Balance at 30 June 2020		4.403	(594)	(278.650)	127.569

Condensed Consolidated Statement of Cash Flow

For the period ended 30 June

Amounts in €'000	HY 2020	HY 2019
Operating result	32.311	24.632
Non-cash adjustments: Depreciation, amortisation, impairment Accrued employee benefits Release contract liabilities	3.122 1.391 -	2.794 1.350 (400)
Operating cash flows before changes in working capital Changes in working capital: Inventories Trade and other receivables Payables and other current liabilities Total changes in working capital	36.824 (1.756) (649) 5.828 3.423	28.376 4.610 (7.379) 170 (2.599)
Changes in non-current assets, liabilities and equity Cash generated from (used in) operations before interest and taxes	(33) 40.214	(605) 25.172
Income taxes paid	(50)	(625)
Net cash flows generated from (used in) operating activities	40.164	24.547
Capital expenditure for property, plant and equipment Investment intangible assets Investment in associates Acquisition of license	(1.035) (230) (13) (7.939)	(1.216) (521) (2.503) -
Net cash flows used in investing activities	(9.217)	(4.240)
Repayment on loans and borrowings Proceeds of issued convertible bonds Payment on contingent consideration Interests on loans and leases Payment of lease liabilities Interest received Proceeds of equity and warrants	(49.914) 122.682 (18.135) (720) (1.402) 479 1.916	(15.533) - (17.635) (4.830) (619) 475 992
Net cash flows generated from (used in) financing activities	54.906	(37.150)
Increase (decrease) of cash Exchange rate effects Cash and cash equivalents at 1 January	85.853 634 68.567	(16.843) 593 81.515
Total cash and cash equivalents at 30 June	155.054	65.265

The notes are an integral part of these interim financial statements

Notes to the Condensed Consolidated Interim Financial Statements For the period ended 30 June

1. Company information

Pharming Group N.V. is a limited liability public company which is listed on Euronext Amsterdam (PHARM), with its headquarters and registered office located at:

Darwinweg 24 2333 CR Leiden The Netherlands

2. Basis of preparation

The consolidated interim financial statements for the six-month ended 30 June 2020 have been prepared in accordance with Accounting Standard IAS 34, Interim financial reporting. The condensed interim financial statements should be read in conjunction with the annual financial statements for the year ended 31 December 2019, which have been prepared in accordance with International Financial Reporting Standards (IFRS) and IFRS Interpretations Committee (IFRS IC) interpretations applicable to companies reporting under IFRS as endorsed by the European Union and valid as of the balance sheet date.

3. Accounting policies

Accounting policies are consistent with those of the financial statements for the year ended 31 December 2019.

4. Estimates and judgements

The preparation of interim financial statements in conformity with IFRS requires the use of certain critical accounting estimates. It also requires management to exercise its judgement in the process of applying the Company's accounting policies. In preparing these condensed interim financial statements, the significant judgements made by management in applying the Company's accounting policies were the same as those applied to the consolidated financial statements for the year ended 31 December 2019.

5. Going concern

In preparing and finishing the interim financial statements the Board of Management of Pharming has assessed the Company's ability to fund its operations for a period of at least eighteen months after the date the interim financial statements are issued. Based upon the assessment on a going concern basis, the Company has concluded that funding of its operations for a period of eighteen months, after the date the interim financial statements are issued, is realistic and achievable. Overall, based on the outcome of this assessment, the interim financial statements have been prepared on a going concern basis.

6. Seasonality of operations

Seasonality has no material impact on Company's interim financial statements.

1. Segment information

The Board of Management is the chief operating decision-maker. The Board of Management considers the business from both a geographic and product perspective. From a product perspective, the Company's business is almost exclusively related to the recombinant human C1 esterase inhibitor business. From a geographic perspective, the Company is operating in the areas: the US, Europe and Rest of the World (RoW). The Board of Management primarily measures revenues to assess the performance of the operating areas. Costs and assets are not allocated to the geographic areas.

Total revenues and gross profit per geographic segment for the period ended 30 June:

Amounts in € '000	HY 2020	HY 2019
Revenues:
US	84.982	75.018
Europe	3.158	2.105
RoW	453	812
Total revenues	88.593	77.935
Gross profit:
US	77.068	66.194
Europe	1.282	202
RoW	385	583
Total gross profit	78.735	66.979

8. Expenses by nature

Cost of sales in the first half year of 2020 amounted to €9.9 million (HY 2019: €11.0 million). Inventory impairments amounted to a release of € (0.3) million in the first half of 2020 (2019: addition of €0.5 million). The impairment stems from the valuation of the inventories against lower net realisable value, related to reallocation of inventories to the different markets with different prices, based on sales forecasts by management and commercial partners, and clinical programmes.

Operating costs increased to €46.9 million from €42.5 million in the first half year of 2019. The increase is a result of the increased sales activities in the US, increased development costs for both our current product as the new pipeline, and increased cost for strengthening of supporting departments.

Employee benefits

Employee benefits are charged to research and development costs, general and administrative costs or marketing and sales costs based on the nature of the services provided.

Depreciation and amortisation charges

Amounts in € '000	HY 2020	HY 2019
Property, plant and equipment	(840)	(679)
Right-of-use assets	(784)	(674)
Intangible assets	(1.759)	(1.440)
Total	(3.383)	(2.793)

The depreciation on right-of-use assets relates to leased buildings and cars.

The amortisation of the intangible assets mainly relates to the re-acquired US commercialisation rights and are allocated to marketing and sales costs in the statement of income.

9. Financial expenses

Amounts in € '000	HY 2020	HY 2019
Foreign currency results	634	-
Interest income	487	475
Contingent consideration	-	31
Other financial income	1.121	506
Foreign currency results	-	(208)
Interest loans and borrowings	(449)	(6.229)
Exit fees and expenses	(3.672)	-
Interest on convertible bonds	(1.944)	-
Other interest expenses	(382)	(330)
Contingent consideration	(1.216)	-
Other financial expenses	(78)	-
Other financial expenses	(7.741)	(6.767)
Total other financial income and expenses	(6.620)	(6.261)

The exit fees and expenses relate to the repayment in full of the loan from Orbimed Royalty Opportunities II, LP.

10. Share of net profits in associates using the equity method

On April 7th, 2019 Pharming Group, through its 100% subsidiary Pharming Technologies B.V., has taken a 43,85% stake in BioConnection B.V. through conversion of EUR 2.6 million of existing credits ("prepayments") and EUR 2.5 million of cash payment for a total of EUR 5.1 million.

In the Board of Management's judgement, the investment in BioConnection constitutes an investment in an unconsolidated structured entity, as Pharming has significant influence but does not have control of BioConnection and is embargoed by a shareholders agreement between the shareholders of BioConnection from influencing any activity between the two parties which is in any significant way different from the relationship which existed between the two prior to the investment. In addition to its carrying value for the investment, Pharming's risk is limited to the provision of a €3 million corporate guarantee in favour of ABN AMRO Bank in the unlikely event that BioConnection were to default on all its debts and its assets did not meet the outstanding liabilities owing to ABN AMRO Bank. In the opinion of the Board of Management, the fact that BioConnection is a growing profitable company which has met all its obligations as they became due since inception makes the likelihood of this guarantee ever being used very small. The guarantee is accounted for under IFRS 9 and appears as financial guarantee liabilities in Other financial liabilities.

The carrying amount of this investment has changed as follows:

Amounts in € '000	30 June 2020	31 December 2019
Balance at 1 January	5.508	-
Carrying value initial recognition	-	5.078
Recognition of financial guarantee	-	221
Amortization of financial guarantee	(13)	(20)
Profit (loss) for the period	121	229
Balance at end of period	5.616	5.508

11. Inventories

Inventories include batches of RUCONEST® drug substance and product and skimmed milk available for production of RUCONEST®.

The inventory valuation at 30 June 2020 of €16.2 million (31 December 2019: €14.5 million) is stated net of a provision for impairment of €0.4 million (31 December 2019: €0.4 million) and net of a provision for obsolescence of €0 million (31 December 2019: €0.4 million).

Amounts in € '000	30 June 2020	31 December 2019
Finished goods	8.436	10.320
Work in progress	5.037	1.843
Raw materials	2.750	2.304
Balance at end of period	16.223	14.467

Changes in the adjustment to net realisable value:

Amounts in € '000	Period to 30 June 2020	Period to 31 December 2019
Balance at 1 January	(830)	(927)
Addition to provision	(536)	(1.010)
Release of provision	797	328
Usage of provision	164	779
Balance at end of period	(405)	(830)

The main portion of inventories at 30 June 2020 has expiration dates starting beyond 2021 and is expected to be sold or used before expiration.

12. Equity

The Company's authorised share capital increased by 10% to €8.8 million and is divided into 880,000,000 ordinary shares with a nominal value of €0.01 each. All 637.703.008 shares outstanding at 30 June 2020 have been fully paid-up. Other reserves include those reserves related to currency translation, share-based compensation expenses and other equity-settled transactions. In the first half year of 2020 a total of 6.379.541 new shares have been issued resulting from conversion of warrants, the issuance of LTIP shares, and the exercise of options.

Please refer to the condensed consolidated statement of changes in equity.

13. Loans and borrowings

In 2017, the Company entered into a debt facility with Orbimed Royalty Opportunities II, LP to raise US\$100 million (€91.3 million at 2017 exchange rate).

Under the terms and conditions of this debt facility, the lenders provided an amount of US\$100 million secured senior debt funding against 48 months promissory notes with interest of the sum of (i) the Applicable Margin of 11% plus (ii) the greater of (x) One-Month LIBOR and (y) 1.00%. Quarterly repayment of the loan has been started in September 2018. The Company has the option to prepay the loan before its maturity date. As further consideration for the facility, the lenders received a 4% warrant coverage (9,174,372 warrants) with a strike price of €0.455 representing the closing price of Pharming shares immediately prior to the closing date, plus a 2.5% commitment fee of the principal sum and an assignment fee on the maturity date of US\$3.7 million. The warrants have been separated from the loan and recognised in equity. On repayment of the loan on January 25, 2020 the Company had to pay an exit fee of 5%.

Movements of the loan were as follows:

Amounts in € '000	Period to 30 June 2020	Period to 31 December 2019
Carrying value at 1 January	45.590	72.502
Amortised costs (financial income and expenses)	449	11.255
Interest paid (cash flow)	(346)	(8.419)
Repayment and exit fee	(46.140)	(31.406)
Revaluation loan	447	1.658
Carrying value at end of period	-	45.590
- Current portion - Non-current portion	- -	45.590 -

14. Convertible bonds

In January 2020, the Company offered €125 million of 5-year convertible bonds. The net proceeds of the issue of the bonds were used to redeem the balance of approximately US\$ 51 million of the loan with Orbimed Advisors in full, and the remaining balance of the net proceeds will also be used to support capital expenditure in relation to the expansion of the commercialisation and manufacturing infrastructure of the Company and also serve as funding for the launch of Pharming's recently acquired leniolisib product, as well as for additional acquisitions/in-licensing opportunities.

The bonds were issued at par and carry a coupon of 3.00% per annum payable semi-annually in arrears in equal instalments. Unless previously converted, redeemed or purchased and cancelled, the Bonds will be redeemed at par on 21 January 2025. The Bonds will be convertible into ordinary shares of the Company with an initial conversion price of €2.0028, which represented a premium of 40% above the volume weighted average price (VWAP) of an ordinary Pharming share on Euronext Amsterdam between opening of trading on the launch date and the pricing of the Bonds (which was €1.4306). This initial conversion price may be subject to customary adjustment provisions as set out in the terms and conditions of the Bonds. The number of ordinary shares initially underlying the Bonds is 62,412,622, representing 9.9% of the Company's current issued share capital.

These bonds are listed on the Frankfurt Exchange (Börse Frankfurt: PHARMING GRP 20/25 CV).

The convertible bonds comprise of two components. The first component is a financial liability, which represents Pharming's contractual obligation to deliver cash or another financial asset for payment of interest and principal, if not converted. The second component is an equity instrument as it represents a written call option granting the holder the right, for a specified period of time, to convert it into a fixed number of Pharming Group N.V. 's ordinary shares.

The fair value of the consideration in respect of the liability components is measured at the fair value of a similar liability that does not have any associated equity conversion option (IFRS 9 paragraph 5.1.1). This is the liability component's carrying amount at initial recognition.

The equity component will be measured at the residual difference between the nominal value and the fair value of a similar liability that does not have any asoociated equity conversion option ( IAS 32 paragraph 31).

Movements of the convertible bonds were as follows:

Amounts in € '000	Period to 30 June 2020
Balance at 1 January	-
Carrying value initial recognition	121.277
Interest paid (cash flow)	-
Amortization transaction cost	301
Accrued interest	1.644
Carrying value at end of period	123.222

15. Fully-diluted shares

The total number of outstanding shares at 30 June 2020 was 637.703.008. The weighted average shares outstanding over the first half year were 634.155.889. The basic earnings per share, based on the weighted average, was € 0.029 for the first half year 2020.

For the first six month of 2020 and 2019, the basic and fully diluted profit per share were:

Amounts in € '000	HY 2020	HY 2019
Net profit (loss) attributable to equity owners of the parent (in €'000)	18.143	13.594
Weighted average shares outstanding (in '000)	634.156	623.157
Basic profit (loss) per share (in €)	0,029	0,022
Weighted average fully-diluted shares outstanding (in '000)	738.277	666.094
Fully-diluted profit per share (in €)	0,025	0,020

Since the reporting date, the company has issued 40.000 shares through the exercise of employee options. The number of issued shares as at 30 July 2020 is 637.743.008.

The composition of the number of shares and share rights outstanding as well as authorised share capital as at 30 June 2020 is provided in the following table:

	31 December 2019	Shares issued	Shares reserved	30 June 2020
Issued shares	631.323.467	6.379.541	-	637.703.008
Warrants	208.944	-	-	208.944
Options	40.327.537	(3.840.107)	-	36.487.430
Convertible bonds	-	-	62.412.622	62.412.622
LTIP	7.644.971	(3.513.263)	-	4.131.708
Fully-diluted shares	679.504.919	(973.829)	62.412.622	740.943.712
Available for issue	120.495.081	80.973.829	(62.412.622)	139.056.288
Authorised share capital	800.000.000	80.000.000	-	880.000.000

	30 June 2020	Shares issued	Shares reserved	30 July 2020
Issued shares	637.703.008	40.000	-	637.743.008
Warrants	208.944	-	-	208.944
Options	36.487.430	(40.000)	(131)	36.447.299
Convertible bonds	62.412.622	-	-	62.412.622
LTIP	4.131.708	-	-	4.131.708
Fully-diluted shares	740.943.712	-	(131)	740.943.581
Available for issue	139.056.288	-	131	139.056.419
Authorised share capital	880.000.000	-	-	880.000.000

16. Intangible Assets

In 2020 intangible assets increased mainly as result of the payment of €7.5 million, related to the reacquisition of the EU commercial rights, formerly owned by SOBI.

17. Deferred tax assets

The changes in the deferred tax asset can be summarised as the result of the payment of the contingent consideration of €16.5 million, leading to a tax effect of €4.1 million, and in addition taxable profits realised during H1 2020.

18. Events since the end of the reporting period

There have been no significant changes or material events since the reporting date.

Appendix: Main Condensed Consolidated Interim Financial Statements reported in US dollars

Condensed Consolidated Statement of Income in US Dollars For the period ended 30 June

Amounts in \$ '000	HY 2020	HY 2019
Revenues	97.827	88.152
Costs of sales	(10.885)	(12.392)
Gross profit	86.942	75.760
Other income	525	167
Research and development	(17.658)	(16.827)
General and administrative	(9.846)	(7.739)
Marketing and sales	(24.283)	(23.500)
Costs	(51.787)	(48.066)
Operating result	35.680	27.861
Fair value gain (loss) on revaluation derivatives	93	(9)
Other financial income	1.237	572
Other financial expenses	(8.252)	(7.654)
Financial income and expenses	(6.922)	(7.091)
Share of net profits in associates using the equity method	134	338
Result before income tax	28.892	21.108
Income tax credit (expense)	(8.561)	(5.732)
Net result for the year	20.331	15.376
Attributable to:
Owners of the parent	20.331	15.376
Total net result	20.331	15.376
Basic earnings per share (\$)	0,032	0,025
Fully-diluted earnings per share (\$)	0,028	0,023

Condensed consolidated Balance Sheet in US Dollars

As at date shown

Amounts in \$ '000	30 June 2020	31 December 2019
Intangible assets	86.532	79.405
Property, plant and equipment	9.803	9.591
Right-of-use assets	5.921	6.705
Deferred tax assets	25.305	32.061
Investments accounted for using the equity method	6.293	6.177
Restricted cash	2.547	2.543
Non-current assets	136.401	136.482
Inventories	18.180	16.223
Trade and other receivables	29.568	28.861
Cash and cash equivalents	171.208	74.348
Current assets	218.956	119.432
Total assets	355.357	255.915
Share capital	7.146	7.079
Share premium	443.794	439.887
Legal reserves	4.268	4.169
Accumulated deficit	(312.255)	(333.749)
Shareholders' equity	142.954	117.387
Convertible bonds	138.082	-
Lease liabilities	4.632	4.893
Other financial liabilities	20.505	36.643
Non-current liabilities	163.219	24.273
Loans and borrowings	-	51.125
Derivative financial liabilities	207	301
Trade and other payables	47.244	40.647
Lease liabilities	1.733	2.182
Other financial liabilities	-	20.000
Current liabilities	49.184	94.484
Total equity and liabilities	355.357	255.915

Condensed consolidated Statement of Cash Flows in US Dollars For the period ended 30 June

Amounts in \$'000	HY 2020	HY 2019
Operating result	35.680	27.861
Non-cash adjustments:
Depreciation, amortisation, impairment	3.447	3.160
Accrued employee benefits	1.536	1.527
Release contract liabilities	-	(452)
Operating cash flows before changes in working capital	40.663	32.096
Changes in working capital:
Inventories Trade and other receivables	(1.939) (717)	5.214 (8.346)
Payables and other current liabilities	6.435	192
Total changes in working capital	3.779	(2.940)
Changes in non-current assets, liabilities and equity	(36)	(684)
Cash generated from (used in) operations before interest and taxes	44.406	28.472
Income taxes paid	(55)	(707)
Net cash flows generated from (used in) operating activities	44.351	27.765
Capital expenditure for property, plant and equipment	(1.143)	(1.375)
Investment intangible assets	(254)	(589)
Investment in associates	(14)	(2.832)
Acquisition of license	(8.767)	-
Net cash flows used in investing activities	(10.178)	(4.796)
Repayment on loans and borrowings Proceeds of issued convertible bonds	(55.117) 135.470	(17.569) -
Payment on contingent consideration	(20.025)	(19.947)
Interests on loans and leases	(795)	(5.463)
Payment of lease liabilities	(1.548)	(700)
Interest received	529	538
Proceeds of equity and warrants	2.116	1.122
Net cash flows generated from (used in) financing activities	60.630	(42.020)
Increase (decrease) of cash	94.803	(19.051)
Exchange rate effects	2.061	123
Cash and cash equivalents at 1 January	76.891	93.245
Total cash and cash equivalents at 30 June	173.755	74.317

--Ends--