Innate Pharma Reports First Half 2022 Financial Results and Business Update
Innate Pharma reported consolidated financial results for the first half of 2022, showcasing a net income of €6.3 million compared to a net loss of €23.7 million in the same period last year. Revenue surged to €45.6 million, primarily driven by milestone payments and collaborations with AstraZeneca and Sanofi. Notably, the company advanced the anti-CD39 monoclonal antibody IPH5201 into Phase 2 trials and received a €3 million milestone for IPH6401/sar514. With a strong cash position of €158.2 million, Innate is well-funded through H2 2024.
- Net income of €6.3 million vs. a net loss of €23.7 million in H1 2021.
- Revenue increased to €45.6 million from €14.7 million in H1 2021.
- Received €3 million milestone payment from Sanofi for IPH6401/sar514.
- Advancement of IPH5201 to Phase 2 clinical trials in collaboration with AstraZeneca.
- Operating expenses rose to €37.1 million, up from €33.9 million in H1 2021.
- R&D expenses increased by €3.7 million primarily due to clinical program costs.
-
Monalizumab and IPH5201 developed in collaboration with AstraZeneca advanced into Phase 3 and 2 clinical trials in lung cancer, triggering
$55M
-
Second preclinical asset based on Sanofi’s proprietary multifunctional CROSSDILES® platform and Innate’s proprietary multi-specific NK cell engager platform, ANKETTM targeting BCMA, selected by Sanofi for IND-enabling studies, with
€3M milestone payment
-
Cash position of
€158.2 million1 as ofJune 30, 2022 , anticipated cash runway into H2 2024 -
Conference call to be held today at
2:00 p.m. CEST /8:00 a.m. EDT
“Based on our strong financial position, we continued the momentum in our product pipeline during the second quarter of the year. We are advancing our anti-CD39 blocking monoclonal antibody IPH5201 to a Phase 2 clinical trial in lung cancer with AstraZeneca, and Sanofi selected a second asset for development, targeting BCMA, that benefits from ANKETTM, Innate’s proprietary multi-specific NK cell engager platform and Sanofi’s CROSSDILES® platform. The ANKETTM technology is the engine for development of our robust pipeline of much needed novel solutions to treat cancer.” said
Webcast and conference call will be held today at |
Access to live webcast: |
https://event.on24.com/wcc/r/3824660/86089F900A17B3EA55F4BEE49AD268A8 |
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Participants may also join via telephone by registering in advance of the event at |
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Upon registration, participants will be provided with dial-in numbers, a direct event passcode and |
a unique registrant ID that they may use 10 minutes prior to the event start to access the call. |
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This information can also be found on the Investors section of the |
A replay of the webcast will be available on the Company website for 90 days following the event. |
Pipeline highlights:
Lacutamab (anti-KIR3DL2 antibody):
- The Phase 2 TELLOMAK study in Sézary syndrome and mycosis fungoides continues to progress and the Company expects to report preliminary data from both cohorts in the second half of 2022.
-
Preliminary results from the TELLOMAK Phase 2 study of lacutamab in patients with advanced mycosis fungoides according to KIR3DL2 expression will be presented at the EORTC-CLTG (
European Organisation for Research and Treatment of Cancer -Cutaneous Lymphoma Tumours Group ) 2022 meeting inMadrid on Friday 23 September.
-
Two clinical trials are underway evaluating lacutamab in patients with KIR3DL2-expressing, relapsed/refractory peripheral T-cell lymphoma (PTCL):
- Phase 1b trial: a Company-sponsored Phase 1b clinical trial to evaluate lacutamab as a monotherapy in patients with KIR3DL2-expressing relapsed PTCL.
-
Phase 2 KILT (anti-KIR in T Cell Lymphoma) trial:
The Lymphoma Study Association (LYSA) investigator-sponsored, randomized trial to evaluate lacutamab in combination with chemotherapy GEMOX (gemcitabine in combination with oxaliplatin) versus GEMOX alone in patients with KIR3DL2-expressing relapsed/refractory PTCL.
-
On the 11 September, at the ESMO (
European Society for Medical Oncology ) 2022 conference, the Company presented a poster on ongoing lacutamab Phase 1b trial design in monotherapy in PTCL.
ANKET™ (Antibody-based NK cell Engager Therapeutics):
- The Phase 1/2 clinical trial by Sanofi continues, evaluating IPH6101/SAR’579, the first NKp46/CD16-based NK cell engager, in patients with relapsed or refractory acute myeloid leukemia (R/R AML), B-cell acute lymphoblastic leukemia (B-ALL) or high-risk myelodysplastic syndrome (HR-MDS).
-
During the period, Sanofi informed the Company of the decision to progress IPH6401/SAR’514 into investigational new drug (IND)-enabling studies, triggering a
€3 million milestone payment. IPH6401/SAR’514 is a BCMA-targeting NK cell engager using Sanofi’s proprietary CROSSODILE® multi-functional platform, which comprises the Cross-Over-Dual-Variable-Domain (CODV) format. It induces a dual targeting of the NK activating receptors, NKp46 and CD16, for an optimized NK cell activation, based on Innate’s ANKETTM proprietary platform. IPH6401/SAR’514 has shown anti-tumor activity and promising drug properties in pre-clinical models. Sanofi will be responsible for all future development, manufacturing and commercialization of IPH6401/SAR’514.
- Innate plan to provide updates on IPH65, the tetra-specific ANKETTM, throughout the year as progress is made toward IND-enabling studies in 2023.
Monalizumab (anti-NKG2A antibody), partnered with AstraZeneca:
-
On
April 29 , Innate announced a$50 million
-
Detailed results from the randomized AstraZeneca-sponsored Phase 2 COAST clinical trial, including monalizumab data in combination with durvalumab, were published in the
Journal of Clinical Oncology onApril 22 . The results were initially presented during theESMO Congress 2021. The results of the interim analysis showed monalizumab in combination with durvalumab improved progression-free survival (PFS) and objective response rate (ORR) compared to durvalumab alone in patients with unresectable, Stage III NSCLC who had not progressed after concurrent CRT.The Journal of Clinical Oncology publication now includes exploratory subgroup analysis.
-
On
April 11 at theAmerican Association for Cancer Research (AACR) Annual Meeting, there was an oral presentation from the AstraZeneca-sponsored Phase 2 NeoCOAST randomized trial in resectable, early-stage NSCLC. The presentation highlighted improved disease responses with durvalumab in combination with monalizumab, oleclumab or danvatirsen, when compared to durvalumab alone. The follow-up randomized Phase 2 clinical trial, NeoCOAST-2, is enrolling patients with resectable, stage IIA-IIIA NSCLC to receive neoadjuvant durvalumab combined with chemotherapy and either oleclumab or monalizumab, followed by surgery and adjuvant durvalumab plus oleclumab or monalizumab.
-
As a post-period event, on
August 1 , Innate announced that a planned futility interim analysis of the INTERLINK-1 study Phase 3 sponsored by AstraZeneca did not meet a pre-defined threshold for efficacy. The company announced that, based on the result and the recommendation of an Independent Data Monitoring Committee, the study was to be discontinued. There were no new safety findings. AstraZeneca plan to share the data in due course. The INTERLINK-1 study, sponsored by AstraZeneca, evaluated monalizumab in combination with cetuximab vs. cetuximab in patients with recurrent or metastatic squamous cell carcinoma of the head and neck who have been previously treated with platinum-based chemotherapy and PD-(L)1 inhibitors.
- On the 12 September at the ESMO 2022 congress, AstraZeneca presented an oral presentation on the Phase 2 NeoCOAST study assessing the safety and efficacy of neoadjuvant durvalumab in combination with chemotherapy and oleclumab or monalizumab and adjuvant treatment in patients with resectable, early-stage NSCLC.
IPH5201 (anti-CD39), partnered with AstraZeneca:
-
On
June 3 , Innate announced that IPH5201, an anti-CD39 blocking monoclonal antibody developed in collaboration with AstraZeneca, will advance into a Phase 2 clinical trial in lung cancer. Innate received inAugust 2022 a$5 million
IPH5301 (anti-CD73):
- The investigator-sponsored Phase 1 trial of IPH5301 (CHANCES), in collaboration with Institut Paoli-Calmettes is underway. The trial will be conducted in two parts, Part 1, the dose escalation, followed by a Part 2 safety expansion study cohort. Part 2 will evaluate IPH5301 in combination with chemotherapy and trastuzumab in HER2+ cancer patients.
Preclinical updates:
- During the period, the Company received from AstraZeneca a notice that it will not exercise its option to license the four preclinical programs covered in the "Future Programs Option Agreement". This option agreement was part 2018 multi-term agreement between AstraZeneca and Innate. Innate has now regained full rights to further develop the four preclinical molecules.
Corporate Update:
-
On
May 03 , Innate announced the commencement of an At-The-Market (ATM) program, pursuant to which it may, from time to time, offer and sell to eligible investors a total gross amount of up to$75 million June 30, 2022 , the balance available under ourMay 2022 sales agreement remains at$75 million
-
Announced on
20 May 2022 , as part of the resolutions voted by shareholders, DrSally Bennett was appointed as new member of the Supervisory Board. She was appointed as a member of the Audit Committee during the Supervisory Board Meeting ofMay 20, 2022 . On the same day it was announced that MrPatrick Langlois decided to resign from his mandate of Supervisory Board member ofInnate Pharma .
Financial highlights for the first half of 2022:
The key elements of Innate’s financial position and financial results as of and for the six-month period ended
-
Cash, cash equivalents, short-term investments and financial assets amounting to
€158.2 million (€m) as ofJune 30, 2022 (€159.7m 2 as ofDecember 31, 2021 ).
-
Revenue and other income from continuing operations3 amounted to
€45.6m in the first half of 2022 (€14.7m in the first half of 2021) and mainly comprise of:-
Revenue from collaboration and licensing agreements, which mainly resulted from the partial or entire recognition of the proceeds received pursuant to the agreements with AstraZeneca and Sanofi and which are recognized on the basis of the percentage of completion of the works performed by the Company under such agreements:
-
(i) Revenue from collaboration and licensing agreements for monalizumab increased by
€10.3m to€16.4m in the first half of 2022 (€6.1m in the first half of 2021). This change mainly results from the transaction price increase of€13.4m ($14.0m April 28, 2022 . This change in the transaction price generated a€12.5 million favorable cumulative adjustment in the revenue related to monalizumab agreements for the first half of 2022, partially offset by effects of the decrease in direct monalizumab research and development costs over the period as compared to the first half of 2021, in connection with the Phase 1 & 2 trials maturity; -
(ii) Revenue related to IPH5201 for the six months ended
June 30, 2022 amounted to€4.8m and results from the entire recognition in revenue of the$5.0m August 2022 from AstraZeneca following the signature onJune 1, 2022 of an amendment to the initial contract signed inOctober 2018 . This amendment sets the terms of the collaboration following AstraZeneca’s decision to advance IPH5201 to a Phase 2 study; -
(iii) During the period, the Company received from AstraZeneca a notice that it will not exercise its option to license the four preclinical programs covered in the "Future Programs Option Agreement". This option agreement was part of the 2018 multi-term agreement between AstraZeneca and the Company under which the Company received an upfront payment of
$20.0m €17.4m ). Innate has now regained full rights to further develop the four preclinical molecules. Consequently, the entire initial payment of$20.0m €17.4m was recognized as revenue as ofJune 30, 2022 . -
(iv) During the period, the Company was informed of Sanofi's decision to advance IPH6401/SAR'514 into investigational new drug (IND)-enabling studies. As such, Sanofi has selected a second multispecific antibody engaging NK cells as a drug candidate. This selection triggered a
€3.0m milestone payment from Sanofi to the Company, fully recognized in revenue as ofJune 30, 2022 . This amount was received by the Company onSeptember 9, 2022 .
-
(i) Revenue from collaboration and licensing agreements for monalizumab increased by
-
Government funding for research expenditures of
€4.3m in the first half of 2022 (€6.4m in the first half of 2021).
-
Revenue from collaboration and licensing agreements, which mainly resulted from the partial or entire recognition of the proceeds received pursuant to the agreements with AstraZeneca and Sanofi and which are recognized on the basis of the percentage of completion of the works performed by the Company under such agreements:
-
Operating expenses from continuing operations are
€37.1m in the first half of 2022 (€33.9m in the first half of 2021), of which67.3% (€25.0m ) are related to R&D.-
R&D expenses from continuing operations increased by
€3.7m to€25.0m in the first half of 2022 (€21.2m in the first half of 2021). This change mainly results from (i) a€0.7m increase in direct R&D expenses relating to lacutamab clinical program and to non-clinical programs, notably IPH65, partially offset by the decrease in others clinical programs expenses; (ii) a€1.7m increase in personnel expenses mainly explained by the increase in share-based payments and (iii) the increase in other R&D expenses explained by the provision relating to the payment to be made to Orega Biotech SAS upon receipt of the$5.0m June 1, 2022 .
-
R&D expenses from continuing operations increased by
-
General and administrative (G&A) expenses from continuing operations decreased by
€0.5m to€12.1m in the first half of 2022 (€12.6m in the first half of 2021).
-
A loss on the Lumoxiti discontinued operations amounting to
€0.1m (€6.2m for the first half of 2021). As a reminder, the Company recorded, as ofJune 30, 2021 , a provision for charges relating to the payment of€5.2 million ($6.2 million June 30, 2021 . Persuant to theApril 2022 underlied agreement, the amount of€5.9 million ($6.2 million
-
A net financial loss of
€2.1m in the first half of 2022 (net financial gain of€1.7m in the first half of 2021), principally as a result of the decrease in fair value of certain of our financial instruments due to the negative impact of the COVID-19 health crisis as well as the Ukrainian crisis on the financial markets.
-
A net income of
€6.3m for the first half of 2022 (net loss of€23.7m for the first half of 2021).
The table below summarizes the IFRS consolidated financial statements as of and for the six months ended
In thousands of euros, except for data per share |
|
|
||
Revenue and other income |
45,589 |
14,671 |
||
Research and development expenses |
(24,956) |
(21,208) |
||
General and administrative expenses |
(12,140) |
(12,643) |
||
Operating expenses |
(37,096) |
(33,851) |
||
Operating income (loss) |
8,494 |
(19,179) |
||
Net financial income (loss) |
(2,118) |
1,709 |
||
Income tax expense |
— |
— |
||
Net income (loss) from continuing operations |
6,376 |
(17,470) |
||
Net income (loss) from discontinued operations |
(73) |
(6,249) |
||
Net income (loss) |
6,303 |
(23,719) |
||
Weighted average number of shares ( in thousands) : |
79,754 |
78,998 |
||
- Basic income (loss) per share |
0.08 |
(0.30) |
||
- Diluted income (loss) per share |
0.08 |
(0.30) |
||
-Basic income (loss) per share from continuing operations |
0.08 |
(0.22) |
||
- Diluted income (loss) per share from continuing operations |
0.08 |
(0.22) |
||
-Basic income (loss) per share from discontinued operations |
— |
(0.08) |
||
- Diluted income (loss) per share from discontinued operations |
— |
(0.08) |
(1) Comparative relating to the six months ended |
|
|
|
||
Cash, cash equivalents and financial assets |
158,156 |
159,714 |
||
Total assets |
280,430 |
267,496 |
||
Total shareholders’ equity |
116,333 |
107,440 |
||
Total financial debt |
43,374 |
44,251 |
About
Innate Pharma’s broad pipeline of antibodies includes several potentially first-in-class clinical and preclinical candidates in cancers with high unmet medical need.
Innate is a pioneer in the understanding of Natural Killer cell biology and has expanded its expertise in the tumor microenvironment and tumor-antigens, as well as antibody engineering. This innovative approach has resulted in a diversified proprietary portfolio and major alliances with leaders in the biopharmaceutical industry including Bristol-Myers Squibb, Novo Nordisk A/S, Sanofi, and a multi-products collaboration with AstraZeneca.
Headquartered in
Learn more about
Information about
ISIN code |
FR0010331421 |
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Ticker code |
Euronext: IPH Nasdaq: IPHA |
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LEI |
9695002Y8420ZB8HJE29 |
Disclaimer on forward-looking information and risk factors:
This press release contains certain forward-looking statements, including those within the meaning of the Private Securities Litigation Reform Act of 1995. The use of certain words, including “believe,” “potential,” “expect” and “will” and similar expressions, is intended to identify forward-looking statements. Although the company believes its expectations are based on reasonable assumptions, these forward-looking statements are subject to numerous risks and uncertainties, which could cause actual results to differ materially from those anticipated. These risks and uncertainties include, among other things, the uncertainties inherent in research and development, including related to safety, progression of and results from its ongoing and planned clinical trials and preclinical studies, review and approvals by regulatory authorities of its product candidates, the Company’s commercialization efforts, the Company’s continued ability to raise capital to fund its development and the overall impact of the COVID-19 outbreak on the global healthcare system as well as the Company’s business, financial condition and results of operations. For an additional discussion of risks and uncertainties which could cause the company's actual results, financial condition, performance or achievements to differ from those contained in the forward-looking statements, please refer to the Risk Factors (“Facteurs de Risque") section of the Universal Registration Document filed with the
This press release and the information contained herein do not constitute an offer to sell or a solicitation of an offer to buy or subscribe to shares in
Summary of Interim Condensed Consolidated Financial Statements and Notes as of
Interim Condensed Consolidated Statements of Financial Position |
||||
(in thousand euros) |
||||
|
|
|
||
Assets |
|
|
||
|
|
|
||
Current assets |
|
|
||
Cash and cash equivalents |
102,949 |
103,756 |
||
Short-term investments |
20,401 |
16,080 |
||
Trade receivables and others |
48,447 |
18,420 |
||
Total current assets |
171,797 |
138,256 |
||
|
|
|
||
Non-current assets |
|
|
||
Intangible assets |
43,260 |
44,192 |
||
Property and equipment |
9,556 |
10,174 |
||
Non-current financial assets |
34,806 |
39,878 |
||
Other non-current assets |
149 |
148 |
||
Trade receivables and others - non-current |
13,084 |
29,821 |
||
Deferred tax asset |
7,778 |
5,028 |
||
Total non-current assets |
108,633 |
129,241 |
||
|
|
|
||
Total assets |
280,430 |
267,496 |
||
Liabilities |
|
|
||
|
|
|
||
Current liabilities |
|
|
||
Trade payables and others |
18,667 |
28,573 |
||
Collaboration liabilities – current portion |
14,167 |
7,418 |
||
Financial liabilities – current portion |
30,851 |
30,748 |
||
Deferred revenue – current portion |
9,094 |
12,500 |
||
Provisions - current portion |
782 |
647 |
||
Total current liabilities |
73,561 |
79,886 |
||
|
|
|
||
Non-current liabilities |
|
|
||
Collaboration liabilities – non-current portion |
58,954 |
32,997 |
||
Financial liabilities – non-current portion |
12,523 |
13,503 |
||
Defined benefit obligations |
2,696 |
2,975 |
||
Deferred revenue – non-current portion |
8,333 |
25,413 |
||
Provisions - non-current portion |
253 |
253 |
||
Deferred tax liabilities |
7,778 |
5,028 |
||
Total non-current liabilities |
90,537 |
80,169 |
||
|
|
|
||
Shareholders’ equity |
|
|
||
Share capital |
3,988 |
3,978 |
||
Share premium |
377,998 |
375,220 |
||
Retained earnings |
(272,241) |
(219,404) |
||
Other reserves |
284 |
456 |
||
Net income (loss) |
6,303 |
(52,809) |
||
Total shareholders’ equity |
116,333 |
107,440 |
||
|
|
|
||
Total liabilities and shareholders’ equity |
280,430 |
267,496 |
||
Interim Condensed Consolidated Statements of Income (loss) |
|||
(in thousand euros) |
|||
|
|
|
|
|
|
|
|
Revenue from collaboration and licensing agreements |
41,271 |
8,304 |
|
Government financing for research expenditures |
4,319 |
6,368 |
|
|
|
|
|
Revenue and other income |
45,589 |
14,671 |
|
|
|
|
|
Research and development expenses |
(24,956) |
(21,208) |
|
General and administrative expenses |
(12,140) |
(12,643) |
|
|
|
|
|
Operating expenses |
(37,096) |
(33,851) |
|
|
|
|
|
Net income / (loss) distribution agreements |
— |
— |
|
|
|
|
|
Operating income (loss) |
8,494 |
(19,179) |
|
|
|
|
|
Financial income |
4,048 |
3,490 |
|
Financial expenses |
(6,166) |
(1,781) |
|
|
|
|
|
Net financial income (loss) |
(2,118) |
1,709 |
|
|
|
|
|
Net income (loss) before tax |
6,376 |
(17,470) |
|
|
|
|
|
Income tax expense |
— |
— |
|
|
|
|
|
Net income (loss) from continuing operations |
6,376 |
(17,470) |
|
|
|
|
|
Net income (loss) from discontinued operations |
(73) |
(6,249) |
|
|
|
|
|
Net income (loss) |
6,303 |
(23,719) |
|
|
|
|
|
Weighted average number of shares : (in thousands) |
79,754 |
78,998 |
|
- Basic income (loss) per share |
0.08 |
(0.30) |
|
- Diluted income (loss) per share |
0.08 |
(0.30) |
|
-Basic income (loss) per share from continuing operations |
0.08 |
(0.22) |
|
- Diluted income (loss) per share from continuing operations |
0.08 |
(0.22) |
|
-Basic income (loss) per share from discontinued operations |
— |
(0.08) |
|
- Diluted income (loss) per share from discontinued operations |
— |
(0.08) |
|
(1) Comparative relating to the six months ended |
Interim Condensed Consolidated Statements of Cash Flow |
||||
(in thousand euros) |
||||
|
|
|
||
Net income (loss) |
6,303 |
(23,719) |
||
Depreciation and amortization, net |
2,030 |
2,168 |
||
Employee benefits costs |
192 |
268 |
||
Change in provision for charges |
134 |
4,952 |
||
Share-based compensation expense |
2,596 |
853 |
||
Change in valuation allowance on financial assets |
2,255 |
(1,031) |
||
Gains (losses) on financial assets |
(1,333) |
(443) |
||
Change in valuation allowance on financial instruments |
(100) |
(170) |
||
Gains on assets and other financial assets |
(25) |
(86) |
||
Interest paid |
194 |
160 |
||
Other profit or loss items with no cash effect |
(52) |
(1,476) |
||
Operating cash flow before change in working capital |
12,194 |
(18,524) |
||
Change in working capital |
(10,976) |
(12,638) |
||
Net cash generated from / (used in) operating activities: |
1,218 |
(31,162) |
||
Acquisition of intangible assets, net |
— |
(33) |
||
Acquisition of property and equipment, net |
(420) |
(240) |
||
Purchase of non-current financial instruments |
— |
— |
||
Disposal of property and equipment |
— |
2 |
||
Purchase of other assets |
(1) |
(63) |
||
Interest received on financial assets |
25 |
86 |
||
Net cash generated from / (used in) investing activities: |
(395) |
(247) |
||
Proceeds from the exercise / subscription of equity instruments |
192 |
61 |
||
Repayment of borrowings |
(958) |
(1,127) |
||
Net interest paid |
(194) |
(160) |
||
Net cash generated / (used in) from financing activities: |
(960) |
(1,226) |
||
Effect of the exchange rate changes |
(670) |
(178) |
||
Net increase / (decrease) in cash and cash equivalents: |
(807) |
(32,812) |
||
Cash and cash equivalents at the beginning of the year: |
103,756 |
136,792 |
||
Cash and cash equivalents at the end of the six-months period: |
102,949 |
103,980 |
||
Revenue and other income
The following table summarizes operating revenue for the periods under review:
In thousands of euros |
|
|
||
Revenue from collaboration and licensing agreements |
41,271 |
8,304 |
||
Government funding for research expenditures |
4,319 |
6,368 |
||
Revenue and other income |
45,589 |
14,671 |
(1) Comparative relating to the six months ended |
Revenue from collaboration and licensing agreements
Revenue from collaboration and licensing agreements increased by
The evolution for the first half of 2022 is mainly due to:
-
A
€10.3 million increase in revenue related to monalizumab, to€16.4 million for the six months endedJune 30, 2022 , as compared to€6.1 million for the six months endedJune 30, 2021 . This change mainly results from the transaction price increase of€13.4 million ($14.0 million April 28, 2022 . This change in the transaction price generated a€12.5 million favorable cumulative adjustment in the revenue related to monalizumab agreements for the first half of 2022, partially offset by effects of the decrease in direct monalizumab research and development costs over the period as compared to the first half of 2021, in connection with the Phase 1 & 2 trials maturity. As ofJune 30, 2022 , the deferred revenue related to monalizumab was€17.3 million (€9.0 million as “Deferred revenue—Current portion” and€8.3 million as “Deferred revenue—Non-current portion).
-
A
€4.8 million increase in revenue related to IPH5201 for the six months endedJune 30, 2022 amounted to and results from the entire recognition in revenue of the$5.0 million June 1, 2022 of an amendment to the initial contract signed inOctober 2018 . This amendment sets the terms of the collaboration following AstraZeneca’s decision to advance IPH5201 to a Phase 2 study. The Company will conduct the study. Both parties will share the external cost related to the study and incurred by the Company and AstraZeneca will provide products necessary to conduct the clinical trial.
-
During the period, the Company received from AstraZeneca a notice that it will not exercise its option to license the four preclinical programs covered in the "Future Programs Option Agreement". This option agreement was part of the 2018 multi-term agreement between AstraZeneca and the Company under which the Company received an upfront payment of
$20.0m €17.4m ). Innate has now regained full rights to further develop the four preclinical molecules. Consequently, the entire initial payment of$20.0m €17.4 million was recognized as revenue as ofJune 30, 2022 .
-
A
€1.2 million decrease in revenue from invoicing of research and development costs. Pursuant to our agreements with AstraZeneca, clinical costs for the ongoing Phase 1 trial of avdoralimab and external research and development costs related to IPH5201 are equally shared betweenInnate Pharma and AstraZeneca, resulting in periodic settlement invoices. These costs are invoiced back on a quarterly basis. This change is mainly explained by the decrease in research and development costs incurred by the Company under these agreements.
-
A
€2.0 million increase in revenue from collaboration and research license agreements with Sanofi, to€3.0 million for the six months endedJune 30, 2022 , as compared to€1.0 million for the six months endedJune 30, 2021 . During the period, the Company was informed of Sanofi's decision to advance IPH6401/SAR'514 into investigational new drug (IND)-enabling studies. As such, Sanofi has selected a second multispecific antibody engaging NK cells as a drug candidate. This selection triggered a€3.0 million milestone payment from Sanofi to the Company, fully recognized in revenue as ofJune 30, 2022 . This amount was received by the Company onSeptember 9, 2022 .
Government funding for research expenditures
Government financing for research expenditures decreased by
The Company is again eligible to the SME status under
Operating expenses
The table below presents our operating expenses from continuing operations for the six months periods ended
In thousands of euros |
|
|
||
Research and development expenses |
(24,956) |
(21,208) |
||
General and administrative expenses |
(12,140) |
(12,643) |
||
Operating expenses |
(37,096) |
(33,851) |
(1) Comparative relating to the six months ended |
Research and development expenses
Research and development (“R&D”) expenses from continuing operations increased by
Direct R&D expenses increased by
Also, as of
Personnel and other expenses allocated to R&D increased by
General and administrative expenses
General and administrative expenses from continuing activities decreased by
Personnel expense includes the compensation paid to our employees, and increased by
Non-scientific advisory and consulting expenses mostly consist of auditing, accounting, taxation and legal fees as well as consulting fees in relation to business strategy and operations and hiring services. Non-scientific advisory and consulting expenses decreased by
The fall in other expenses of
Financial income (loss), net
We recognized a net financial loss of
Net loss from discontinued operations
As a reminder, further to the decision to terminate the Lumoxiti Agreement and termination notice sent in
As a consequence, net loss from discontinued operations relating to Lumoxiti for the six months ended
Balance sheet items
Cash, cash equivalents, short-term investments and non-current financial assets amounted to
The other key balance sheet items as of
-
Deferred revenue of
€17.4 million (including€8.3 million booked as ‘Deferred revenue – non-current portion’) and collaboration liabilities of€73.1 million (including€59.0 million booked as ‘Collaboration liabilities - non-current portion’) relating to the remainder of the initial payment received from AstraZeneca not yet recognized as revenue or used as part of the co-financing of the monalizumab program with AstraZeneca;
-
Receivables from the French government amounting to
€44.4 million in relation to the research tax credit for 2019 to 2021 and the six-month period endedJune 30, 2022 ;
-
Intangible assets for a net book value of
€43.3 million , mainly corresponding to the rights and licenses relating to the acquisition of the monalizumab and avdoralimab;
-
Shareholders’ equity of
€116.3 million , including the net income of the period of€6.3 million ;
Cash-flow items
As of
The net cash flow used during the period under review mainly results from the following:
-
Net cash flow used by operations of
€1.2 million for the six months endedJune 30, 2022 as compared to net cash flows used by operations of€31.2 million for the six months endedJune 30, 2021 . This increase mainly results from the collection of€47.7 million , inJune 2022 , following the treatment of the first patient in the second Phase 3 clinical trial evaluating monalizumab, “PACIFIC-9”. This increase is partially offset by the€5.9 million payment to AstraZeneca onApril 20, 2022 persuant to the Lumoxiti termination and transition agreement. As a reminder, net cash flow used in operating activities for the first half of 2021 included€8.0 million of proceeds from Sanofi in January andFebruary 2021 , under the IPH6101/SAR443579 agreement signed in 2016. Restated for these transactions, net cash flow used in operating activities for the first half of 2022 increases by€1.4 million as compared to the first half of 2021. This change results from the increase of the outflows in relation with the Company’s operating activities, notably the net collaboration liabilities outflows related to the monalizumab collaboration agreement. Net cash flow consumed by operating activities in connection with the Lumoxiti discontinued operation amounted to€5.5 million for the first half of 2022, as compared to€4.4 million for the first half of 2021. The amount consumed for the first half of 2022 relates to the payment of€5.5 million ($6.2 million April 2022 in accordance with the Lumoxiti termination and transition agreement effective as ofJune 30, 2021 .
-
Net cash flow used in investing activities of
€0.4 million , as compared to€0.2 million for the first half of 2021. The Company has not made any investments in tangible, intangible or significant financial assets during the first half of 2022 and 2021. Net cash flows consumed by investing activities in connection with the Lumoxiti discontinued operation were nil for the first half of 2022 and 2021, respectively.
-
Net cash flows used in financing activities for the six months ended
June 30, 2022 , are stable as compared to the six months endedJune 30, 2021 . These consumptions are mainly related to repayments of financial liabilities. Net cash flows consumed by financing activities in connection with the Lumoxiti discontinued operation were nil for the first half of 2022 and 2021, respectively.
Post period events
On
In
Nota
The interim consolidated financial statements for the six-month period ended
Risk factors
Risk factors identified by the Company are presented in section 3 of the universal registration document (“Document d’Enregistrement Universel”) submitted to the French stock-market regulator, the “Autorité des Marchés Financiers”, on
Furthermore, the conflict triggered by
Related party transactions:
Transactions with related parties during the periods under review are disclosed in Note 19 to the interim condensed consolidated financial statements for the period ended
| ___________________________ |
1 Including short term investments ( |
2 Cash and cash equivalents included proceeds relating to State-Guaranteed Loans |
3 Comparative relating to the six months ended |
View source version on businesswire.com: https://www.businesswire.com/news/home/20220914005962/en/
Investors
Tel.: +33 (0)4 84 90 32 88
Henry.Wheeler@innate-pharma.fr
Media Relations
NewCap
Tel. : +33 (0)1 44 71 00 15
innate@newcap.eu
Source:
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