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Financial highlights

Consolidated key figures

(thousands of €, if not stated otherwise)

Second quarter of 2022

Second quarter of  2021

Six months ended 30 June 2022

Six months ended 30 June 2021

Year ended 31 Decembe r 2021

Income statement

 

 

 

 

 

Product net sales

20,945

377

35,356

456

14,753

Collaboration revenues

116,665

139,395

238,601

253,207

470,093

Cost of sales

(2,633)

(93)

(5,545)

(131)

(1,629)

R&D expenditure

(149,597)

(138,866)

(249,518)

(268,826)

(491,707)

S&M, G&A expenses

(71,670)

(60,861)

(134,009)

(105,819)

(210,855)

Other operating income

9,957

13,298

17,637

23,564

53,749

Operating loss

(76,332)

(46,750)

(97,478)

(97,548)

(165,596)

Net financial results

58,115

(18,209)

67,676

19,916

42,598

Taxes

(811)

630

(2,536)

473

(2,423)

Net loss from continuing operations

(19,028)

(64,329)

(32,338)

(77,159)

(125,422)

Net profit from discontinued operations, net of tax

-

-

-

22,191

22,191

Net loss

(19,028)

(64,329)

(32,338)

(54,968)

(103,231)

 

 

 

 

 

 

Balance sheet

 

 

 

 

 

Cash and cash equivalents

972,796

2,642,639

972,796

2,642,639

2,233,368

Current financial investments

3,456,184

2,363,969

3,456,184

2,363,969

2,469,809

R&D incentives receivables

155,771

142,745

155,771

142,745

144,013

Assets

5,040,085

5,430,617

5,040,085

5,430,617

5,193,160

Shareholders' equity

2,646,898

2,663,473

2,646,898

2,663,473

2,643,362

Deferred income

2,159,553

2,565,292

2,159,553

2,565,292

2,364,701

Other liabilities

233,634

201,852

233,634

201,852

185,097

 

 

 

 

 

 

Cash flow

 

 

 

 

 

Operational cash burn

(139,721)

(95,527)

(217,102)

(223,196)

(564,840)

Cash flow used in operating activities

(141,772)

(81,922)

(203,740)

(203,131)

(503,827)

Cash flow generated from/used in (-) investing activities

(147,604)

182,194

(1,081,057)

682,053

541,238

Cash flow used in financing activities

(337)

(1,952)

(361)

(1,474)

(3,876)

Increase/decrease (-) in cash and cash equivalents

(289,712)

98,319

(1,285,158)

477,448

33,535

Effect of currency exchange rate fluctuation on cash and cash equivalents

8,229

(9,629)

24,586

22,121

56,763

Cash and cash equivalents at the end of the period

972,796

2,642,639

972,796

2,642,639

2,233,368

Current financial investments at the end of the period

3,456,184

2,363,969

3,456,184

2,363,969

2,469,809

Total current financial investments and cash and cash equivalents at the end of the period

4,428,980

5,006,608

4,428,980

5,006,608

4,703,177

 

 

 

 

 

 

Financial ratios

 

 

 

 

 

Number of shares issued at the end of the period

65,728,511

65,522,521

65,728,511

65,522,521

65,552,721

Basic and diluted loss per share (€)

(0.29)

(0.98)

(0.49)

(0.84)

(1.58)

Share price at the end of the period (in €)

53.04

58.48

53.04

58.48

49.22

Total group employees at the end of the period (number)

1,344

1,397

1,344

1,397

1,309

Employees per site as of 30 June 2022

(total: 1,344 employees)

Employees per site (graph)

H1 2022 financial results

We reported product net sales of Jyseleca in Europe for the first six months of 2022 amounting to €35.4 million (€0.5 million in the first half-year of 2021). Our counterparties for the sales of Jyseleca were mainly hospitals and wholesalers located in Belgium, the Netherlands, France, Italy, Spain, Germany, Great Britain, Ireland, Austria, Norway, Sweden and Finland.

Cost of sales related to Jyseleca net sales in the first six months of 2022 amounted to €5.5 million.

Collaboration revenues amounted to €238.6 million for the first six months of 2022, compared to €253.2 million for the first six months of 2021.

Revenues recognized related to the collaboration agreement with Gilead for the filgotinib development were €115.3 million in the first six months of 2022 compared to €136.1 million for the same period last year. This decrease was due to a lower increase in the percentage of completion, partly offset by a higher revenue recognition of milestone payments strongly influenced by the milestone achieved related to the regulatory approval in Japan for UC in the first half-year of 2022.

The revenue recognition related to the exclusive access rights for Gilead to our drug discovery platform amounted to €114.9 million for the first six months of 2022 (€115.7 million for the same period last year).

We have recognized royalty income from Gilead for Jyseleca for €6.3 million in the first six months of 2022 (compared to €1.4 million in the same period last year) of which €3.6 million royalties on milestone income for UC approval in Japan.

Additionally, we recorded milestones of €2.0 million triggered by the first sale of Jyseleca in Czech Republic and Portugal by our distribution and commercialization partner Sobi, in the first half-year of 2022.

Our deferred income balance on 30 June 2022 includes €1.6 billion allocated to our drug discovery platform that is recognized linearly over the remaining period of our 10 year collaboration, and €0.5 billion allocated to filgotinib development that is recognized over time until the end of the development period.

Our R&D expenditure in the first six months of 2022 amounted to €249.5 million, compared to €268.8 million for the first six months of 2021. This decrease was primarily explained by a decrease in subcontracting costs from €139.2 million in the first half-year of 2021 to €104.1 million in the first half-year of 2022, primarily due to the winding down of the ziritaxestat (IPF) program and reduced spend on our Toledo (SIKi) and TYK2 programs. This was partly offset by cost increases for our filgotinib program, on a six month basis compared to the same period in 2021. Personnel costs decreased from €94.2 million in the first half of 2021 to €86.0 million for the same period this year mainly due to a lower number of FTEs as well as lower costs for our subscription right plans. Depreciation and impairment amounted to €32.6 million for the first six months of 2022 (€8.1 million for the same period last year). This increase was primarily due to an impairment of €26.7 million of previously capitalized upfront fees related to our collaboration with Molecure on the dual chitinase inhibitor OATD-01 (GLPG4716). As part of an ongoing strategic exercise to renew and accelerate our portfolio, we decided to return all rights to OATD-01 to Molecure.

Our S&M expenses were €71.0 million in the first six months of 2022, compared to €29.0 million in the first six months of 2021. This increase was primarily due to the termination of our 50/50 filgotinib co-commercialization cost sharing agreement with Gilead. The cost increase was also explained by an increase in personnel costs (€35.7 million for the first six months of 2022 compared to €26.9 million for the same period last year) explained by an increase in the commercial work force from 215 average FTEs in the first half-year of 2021 to 305 average FTEs in the first half-year of 2022 driven by the commercial launch of filgotinib in Europe.

Our G&A expenses were €63.0 million in the first six months of 2022, compared to €76.9 million in the first six months of 2021. The cost decrease was primarily due to the exceptional impairment of €9.3 million on other tangible assets recorded in the first six months of 2021 following our decision to reassess the construction project of our new future headquarter location in Mechelen (Belgium). Personnel costs (€35.6 million for the first six months of 2022 compared to €37.6 million for the same period last year) decreased primarily explained by a lower number of FTEs.

Other operating income (€17.6 million for the first six months of 2022, compared to €23.6 million for the first six months of 2021) decreased by €5.9 million, mainly driven by lower grant and R&D incentive income.

We reported an operating loss amounting to €97.5 million for the first six months of 2022, compared to an operating loss of €97.6 million for the same period last year.

Net financial income in the first six months of 2022 amounted to €67.7 million (as compared to net financial income of €19.9 million in the same period last year). Net financial income in the first six months of 2022 was primarily attributable to €57.4 million of unrealized currency exchange gain on our cash and cash equivalents and current financial investments at amortized cost in U.S. dollar (as compared to €33.4 million currency exchange gain on cash and cash equivalents and current financial investments in the first six months of 2021) and €11.8 million positive changes in (fair) value of current financial investments (€5.8 million negative changes in the same period last year). The other financial expenses also contained the effect of discounting our long term deferred income of €3.8 million (€4.8 million in the same period last year). The fair value loss of financial assets held at fair value through profit or loss amounted to nil in the first six months in 2022 (as compared to €2.9 million in the same period last year).

We realized a net loss from continuing operations of €32.3 million for the first six months of 2022, compared to a net loss of €77.2 million for the first six months of 2021.

The net profit from discontinued operations for the first six months of 2021 consisted of the gain on the sale of Fidelta, our fee-for-services business, for €22.2 million.

We reported a group net loss for the first six months of 2022 of €32.3 million, compared to a net loss of €55.0 million for the same period last year.

Cash, cash equivalents and current financial investments

Cash and cash equivalents and current financial investments totaled €4,429.0 million on 30 June 2022 (€4,703.2 million on 31 December 2021).

A net decrease of €274.2 million in cash and cash equivalents and current financial investments was recorded during the first six months of 2022, compared to a net decrease of €162.7 million during the first six months of 2021. This net decrease was composed of (i) €217.1 million of operational cash burn, (ii) offset by €3.6 million of cash proceeds from capital and share premium increases from exercise of subscription rights in the first six months of 2022, (iii) €11.8 million of positive changes in (fair) value of current financial investments and €60.4 million of mainly positive exchange rate differences, and (iv) €132.9 million cash out from the acquisitions of CellPoint and AboundBio, net of cash acquired.

The operational cash burn (or operational cash flow if this liquidity measure is positive) is a financial measure that is not calculated in accordance with IFRS. Operational cash burn/cash flow is defined as the increase or decrease in our cash and cash equivalents (excluding the effect of exchange rate differences on cash and cash equivalents), minus:

i. the net proceeds, if any, from share capital and share premium increases included in the net cash flows generated from/used in (–) financing activities

ii. the net proceeds or cash used, if any, in acquisitions or disposals of businesses; the movement in restricted cash and movement in current financial investments, if any, the loans and advances given to third parties, if any, included in the net cash flows generated from/used in (–) investing activities

iii. the cash used for other liabilities related to the acquisition of businesses, if any, included in the net cash flows generated from/used in (-) operating activities.

This alternative liquidity measure is in our view an important metric for a biotech company in the development stage.

The following table provides a reconciliation of the operational cash burn:

 

Six months ended 30 June

(thousands of €)

2022

2021

Increase/decrease (-) in cash and cash equivalents
(excluding effect of exchange differences)

(1,285,158)

477,448

Less:

 

 

Net proceeds from capital and share premium increases

(3,619)

(2,583)

Net purchase/sale (-) of current financial investments

938,732

(669,365)

Cash out from acquisition of subsidiaries, net of cash acquired

115,178

-

Cash advances and loans to third parties

10,000

-

Cash used for other liabilities related to the acquisition of subsidiaries

7,765

-

Cash in from disposals of subsidiaries, net of cash disposed of

-

(28,696)

Total operational cash burn

(217,102)

(223,196)

Filgotinib
Formerly known as GLPG0634, commercial name is Jyseleca. Small molecule preferential JAK1 inhibitor, approved in RA in European Union, Great Britain, and Japan, and in UC in European Union and Great Britain. Application for approval for ulcerative colitis was filed in Japan. Filgotinib is partnered with Gilead. Filgotinib currently is in Phase 3 trials in CD, and in a Phase 4 trial in RA
GLPG4716
A chitinase inhibitor inlicensed from Molecure (previously OncoArendi). The rights to the molecule have been returned to Molecure in July 2022