UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 6-K
REPORT OF FOREIGN PRIVATE ISSUER
PURSUANT TO RULE 13a-16 OR 15d-16
UNDER THE SECURITIES EXCHANGE ACT OF 1934
Date of report:
19 September 2024
Commission
File Number: 001-38844
GENFIT S.A.
(Translation of registrant’s name into English)
Parc Eurasanté
885, avenue Eugène
Avinée
59120 Loos, France
(Address of principal
executive office)
Indicate by check mark whether the registrant files or will file
annual reports under cover of Form 20-F or Form 40-F:
☒
Form 20-F ☐ Form 40-F
INCORPORATION
BY REFERENCE
The contents of this report on
Form 6-K (including Exhibit 99.1) are hereby incorporated by reference into the registrant’s registration statement on Form F-3
(File No. 333-271312) and registration statement on Form S-8 (File No. 333-271311) and related prospectuses, as such registration statements
and prospectuses may be amended from time to time, and to be a part thereof from the date on which this report is filed, to the extent
not superseded by documents or reports subsequently filed or furnished. Information contained on, or that can be accessed through, any
website included in Exhibit 99.1 is expressly not incorporated by reference.
EXHIBIT LIST
SIGNATURES
Pursuant to the requirements of the
Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto
duly authorized.
| |
GENFIT
S.A. |
| |
|
|
| Date:
19 September 2024 |
By: |
|
/s/
Pascal PRIGENT |
| |
|
|
Name:
Pascal PRIGENT |
| |
|
|
Title:
Chief Executive Officer |
Exhibit
99.1
GENFIT Reports
First Half-Year 2024 Financial Results and
Provides
Corporate Update
|
• |
Cash and cash equivalents totaled
€61.6 million as of June 30, 2024, excluding the €48.7 million milestone invoiced in June 2024 (received in August 2024) upon
first sale of Ipsen’s Iqirvo® (elafibranor) in the U.S. for the treatment of Primary Biliary Cholangitis (PBC) |
|
• |
€59.0 million in revenues,
including the €48.7 million milestone invoiced in June 2024 |
|
• |
Positive opinion from the European
Medicines Agency Committee in July 2024, with final decision on marketing authorization for Iqirvo anticipated in the second half of 2024,
clearing the path to an additional €26.5 million milestone payment expected upon Iqirvo’s pricing and reimbursement approval
in three European countries |
Lille
(France), Cambridge (Massachusetts, United States), (Zurich, Switzerland); September 19, 2024 – GENFIT (Nasdaq and Euronext: GNFT),
a late-stage biopharmaceutical company dedicated
to improving the lives of patients with rare and life-threatening liver diseases, today announced its first half-year 2024 financial results
and provided a corporate update.
Pascal
Prigent, CEO of GENFIT, commented:
“The
approval of Iqirvo in the United States was a very significant milestone for the entire GENFIT team. We are proud to have developed elafibranor
from its initial discovery through late-stage trials and are thrilled to now see it prescribed to U.S. patients. We believe Iqirvo can
potentially address a significant unmet need for people living with PBC. Following the positive CHMP opinion in July 2024, we also anticipate
a final decision on authorization in Europe by the end of the year.”
Mr.
Prigent continued, “We believe the recent approval in the U.S. of Iqirvo demonstrates our robust drug development capabilities
and, along with our strong financial position enabled by our partnership with Ipsen, we are well positioned to continue to develop innovative
therapies for challenging and underserved liver conditions that are life-threatening.”
I.
1H24 Business highlights1
PBC
Accelerated
approval of Ipsen’s Iqirvo®2 (elafibranor) was granted on June 10, 2024 by the U.S. Food and Drug Administration
(U.S. FDA), as a first-in-class treatment for PBC in combination with ursodeoxycholic acid (UDCA) in adults with an inadequate response
to UDCA, or as monotherapy in patients unable to tolerate UDCA.
1
The Half Year Business and Financial Report is available to the public and was filed with the French Autorité des Marchés
Financiers (French Financial Markets Authority) and filed with the U.S. Securities and Exchange Commission today. The condensed consolidated
financial statements are included in this press release and the complete financial statements are included in the Half-Year Business and
Financial Report which is available on the “Investors” page of the GENFIT website.
2
Iqirvo®, Elative®, NIS2+® and UNVEIL-IT® are registered trademarks of GENFIT SA
Following
Ipsen’s commercial launch in the U.S. in June 2024, first royalty invoicing began and a €48.7 million milestone payment was
made.
On
July 25, 2024, Ipsen announced an “encouraging early start for Iqirvo in the U.S.” and indicated that “50%
of Healthcare Professionals surveyed one week post launch were very likely to prescribe Iqirvo”. Ipsen also reported “early
positive coverage determinations from commercial and government payer segments”3.
On
July 26, 2024, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency's (EMA) issued a positive opinion
for the treatment of PBC in combination with ursodeoxycholic acid (UDCA) in adults with an inadequate response to UDCA or as a monotherapy
in patients unable to tolerate UDCA.
Acute on-Chronic Liver Failure (ACLF) franchise
The
UNVEIL-IT®2 Phase 2 trial for VS-01 progressed, with the opening of several new clinical investigation sites and geographic
expansion into the U.S. However, the initial uptake of recruitment was below our expectations, and we have been working closely with investigators
to address this. As a result, we have modified our protocol to better account for the logistics of the care for these patients, as well
as their many comorbidities. We feel that the latest version of the protocol addresses the initial challenges and should allow us to maintain
our timeline of having preliminary results before the end of the year. We will monitor the impact of the implementation of the new protocol
and will update this guidance as appropriate.
During
the EASL congress in June 2024, GENFIT presented blood and peritoneal metabolomics data suggesting that VS-01 actively captures metabolites
associated with ACLF. Data indicating that NTZ (nitazoxanide) directly protects from stress-induced cell death to alleviate liver damage
in preclinical models of ACLF were also presented.
June
2024 also marked the start of a research collaboration between GENFIT and the European Foundation for the Study of Chronic Liver Failure
(EF CLIF), reinforcing our leadership in advancing the understanding of ACLF.
MASH diagnostics
In
June 2024, new European Clinical Practice Guidelines on managing metabolic dysfunction-associated steatotic liver disease (MASLD) recognized
NIS2+®2 as a key tool for detecting at-risk MASH4. This highlights the potential of our technology in identifying
those who may benefit from emerging MASH treatments.
Corporate
governance updates
3
www.ipsen.com/websites/ipsen_com_v2/wp-content/uploads/2024/07/24211739/H1-2024-results-presentation.pdf
4
Metabolic dysfunction-associated steatohepatitis
Following
the death of Mr. Xavier Guille des Buttes in April 2024, Vice-Chairman of the Board of Directors, the composition of the Board of Directors
of the Company changed. In accordance with the succession plan, Mr. Éric Baclet become Vice-Chairman of the Board of Directors.
He was also appointed Chairman of the Nominations and Compensation Committee. Mr. Jean-François Tiné joined the Audit Committee.
In May 2024, the Board of Directors appointed Ms. Katherine Kalin as member of the ESG Committee.
II.
2H24 and beyond: key milestones and outlook
PBC
Following
the positive CHMP recommendation, the European Commission is expected to take a final decision on marketing authorization for Iqirvo in
the second half of 2024. After the €13.3 million milestone payment received in February 2024 and the €48.7 million milestone
payment received in August 2024, a €26.5 million milestone payment is expected to be received upon Iqirvo’s pricing and reimbursement
approval in three European countries.
Over
the Summer of 2024, Iqirvo's competitive landscape evolved as expected, reinforcing confidence in our revenue projections. We intend to
provide royalty revenue forecasts once additional information is received from our commercial partner Ipsen5.
ACLF franchise
Previous
guidance is reiterated:
|
• |
VS-01-ACLF: Phase 2 interim data
readout still targeted for 2H24, taking into account the implementation of the new protocol |
|
• |
NTZ in ACLF: reformulation and Phase
2 under preparation with a proof-of-concept study initiation targeted for 1H25 |
|
• |
SRT-015: First-in-Human study initiation
targeted 1Q25 |
|
• |
CLM-022: preclinical Proof of Concept
expected to be obtained by end of 2024 |
|
• |
VS-02-HE: completion of Investigational
New Drug (IND) enabling studies expected in 2025 |
Other
indications
Previous
guidance is reiterated:
|
• |
Cholangiocarcinoma (CCA): The GNS561
Phase 1b/2a clinical trial is currently ongoing and preliminary data from Phase 1b is targeted by the end of 2024 |
5
www.ipsen.com/investors/financial-calendar (www.ipsen.com/event/ytd-2024-sales)
|
• |
VS-01 Urea Cycle Disorder (UCD)
and Organic Acidemia (OA): Following completion of the non-clinical feasibility study, we plan to develop formulation optimization for
specific pediatric implementation and conduct IND enabling nonclinical studies with a target to complete such non-clinical studies in
2024. |
MASH
Diagnostics
The
first-ever approved drug for MASH was approved in early 2024 and we anticipate that this should increase the focus on diagnosis over the
coming years and the need for a non-invasive test such as NIS2+.
III.
1H24 Financial highlights
Cash
and cash equivalents
As
of June 30, 2024,
GENFIT had €61.6 million in cash and cash equivalents compared with €77.8
million as of December 31, 2023. Cash and cash equivalents
as of June 30, 2024 exclude the €48.7 million milestone invoiced in June 2024 upon first sale of Ipsen’s Iqirvo® (elafibranor)
in the U.S. for the treatment of PBC, as this balance was received in August 2024.
We
expect that our existing cash and cash equivalents will enable us to fund our operating expenses and capital expenditure requirements
until at least the start of the fourth quarter of 2025. This is based on current assumptions and programs and does not include exceptional
events. This estimation includes our expectations to receive future milestone revenue, subject to approval by applicable regulatory authorities
and European commercial launches of elafibranor in PBC by Ipsen, representing a total of approximately €26.5 million.
In
the first half of 2024,
cash utilization is mainly the result of our research and development efforts, notably for Elative, our Phase 3 clinical trial
of elafibranor in PBC (approved by the FDA in June 2024); UNVEIL-IT, our Phase 2 clinical trial of VS-01 in ACLF; GNS561, as part of our
cholangiocarcinoma program; NTZ, as part of our ACLF program; and SRT-015, also as part of our ACLF program.
Revenues
and other income
Revenues
and other income amounted to €61.2 million
in the first half of 2024, compared to €15.4 million
in the first half of 2023.
Substantially
all revenue is attributable to our Collaboration and License Agreement with Ipsen and related Transition Services Agreement. Revenue growth
is due to a €48.7 million milestone invoiced to Ipsen in June 2024 following the first commercial sale of Iqirvo in the U.S. The
milestone was collected in August 2024.
Operating
expenses
Operating
expenses amounted to €30.0 million
in the first half of 2024, compared to €34.7 million
in the first half of 2023).
Substantially
all of the decrease in operating expenses is due to research and development expenses, which amounted to €19.0
million in the first half of 2024 (compared to €25.6
million in the first half of 2023).
Specifically,
there was a decrease in:
|
• |
Contracting costs which amounted
to €7.8 million in the first half of 2024 (compared to €14.4 million in the first half of 2023), primarily reflecting decreased
activities related to Elative, following the FDA approval in June 2024, and |
|
• |
Other expenses (maintenance, fees,
travel and other taxes) which amounted to €2.8 million in the first half of 2024 (compared to €3.3 million in the first half
of 2023), reflecting decreased activity as previously noted. |
Financial
results
For
the half-year ended June 30, 2024, financial income amounted to a loss of €0.9 million, compared to a loss of €1.1 million
for the same period in 2023.
Net
loss
The
first half of 2024 resulted
in a net profit of €30.3 million, compared with a net loss of €20.9 million
in the first half of 2023.
The
table below presents the condensed Consolidated Statement of Operations under the International Financial Reporting Standards (IFRS) for
the first half of 2024,
with comparative figures for the first half of 2023.
| |
|
Half-year ended |
| (in € thousands, except earnings per share data) |
|
|
2023/06/30 |
|
|
|
2024/06/30 |
|
| |
|
|
|
|
| Revenues and
other income |
|
|
|
|
|
|
|
|
| Revenue |
|
|
11,482 |
|
|
|
58,973 |
|
| Other income |
|
|
3,893 |
|
|
|
2,226 |
|
| Revenues and other income |
|
|
15,374 |
|
|
|
61,199 |
|
| |
|
|
|
|
|
|
|
|
| Operating
expenses and other operating income (expenses) |
|
|
|
|
|
|
|
|
| Research and development expenses |
|
|
(25,630 |
) |
|
|
(18,984 |
) |
| General and administrative expenses |
|
|
(9,105 |
) |
|
|
(10,564 |
) |
| Marketing and market access expenses |
|
|
(520 |
) |
|
|
(390 |
) |
| Reorganization and restructuring income (expenses) |
|
|
633 |
|
|
|
0 |
|
| Other operating expenses |
|
|
(52 |
) |
|
|
(39 |
) |
| |
|
|
|
|
|
|
|
|
| Operating income (loss) |
|
|
(19,299 |
) |
|
|
31,222 |
|
| |
|
|
|
|
|
|
|
|
| Financial income |
|
|
1,748 |
|
|
|
1,546 |
|
| Financial expenses |
|
|
(2,890 |
) |
|
|
(2,419 |
) |
| Financial profit (loss) |
|
|
(1,141 |
) |
|
|
(873 |
) |
| |
|
|
|
|
|
|
|
|
| Net profit (loss) before
tax |
|
|
(20,440 |
) |
|
|
30,349 |
|
| |
|
|
|
|
|
|
|
|
| Income tax benefit (expense) |
|
|
(414 |
) |
|
|
(39 |
) |
| |
|
|
|
|
|
|
|
|
| Net profit (loss) |
|
|
(20,854 |
) |
|
|
30,311 |
|
| |
|
|
|
|
|
|
|
|
| Basic and diluted earnings (loss) per share |
|
|
|
|
|
|
|
|
| Basic earnings (loss) per share (€/share) |
|
|
(0.42 |
) |
|
|
0.61 |
|
| Diluted earnings (loss) per share (€/share) |
|
|
(0.42 |
) |
|
|
0.53 |
|
Further
information is provided in the condensed consolidated financial statements at June
30, 2024 under the IFRS and the management discussion of the results are provided in the appendix
of this press release. The condensed consolidated financial statements as well as the statutory auditors' report on those financial statements
are included in the 2024 Half Year Business and Financial Report available on the “Investors”
page of the GENFIT website.
We
encourage investors to take into consideration all the information presented in our 2023 Annual Report on Form 20-F (“Form 20-F”)
filed with the U.S. Securities Exchange Commission and the 2023 Universal Registration Document filed under D.24-0246 with the French
Autorité des Marchés Financiers (AMF) on April 5, 2024 and the 2024 Half-Year Business and Financial Report before deciding
to invest in Company shares; these documents are available on GENFIT’s website: www.genfit.com and on the website of the AMF (www.amf-france.org).
This includes, in particular, the risk
factors described in Item 3 of the Form 20-F (and the contents of this section) and section 2 of the 2023 Universal Registration Document,
as well as the update provided in section 2.5 of the 2024 Half-Year Business and Financial Report,
of which the realization may have (or has had in some cases) material adverse effect on the Group and its activity, financial situation,
results, development or perspectives, and which are of importance in the investment decision-making process.
APPENDICES
| |
Half-year
Consolidated Financial Results at June 30, 2024 |
|
| |
|
The
Condensed Consolidated Statements of Financial Position, Statements of Operations and Statements of Cash Flow of the Group were prepared
in accordance with the IFRS.
The
limited review procedures on the condensed consolidated financial statements have been performed. The half-year consolidated financial
statements for the period ended June 30, 2024 were
approved by the Board of Directors on September 18, 2024.
The
condensed consolidated financial statements as well as the notes to the consolidated financial statements for the period ended June
30, 2024 and the statutory auditor’s report on the consolidated financial statements are included
in the Half Year Business and Financial Report at June 30, 2024 available on the “Investors”
page of the GENFIT website.
All
financial information (unless indicated otherwise) is presented in thousands of euros (€).
Condensed
Consolidated Statement of Financial Position
Assets
| |
|
As of |
| (in € thousands) |
|
|
2023/12/31 |
|
|
|
2024/06/30 |
|
| Current assets |
|
|
|
|
| Cash and cash equivalents |
|
|
77,789 |
|
|
|
61,645 |
|
| Current trade and others receivables |
|
|
32,707 |
|
|
|
71,044 |
|
| Other current assets |
|
|
2,615 |
|
|
|
3,690 |
|
| Inventories |
|
|
4 |
|
|
|
4 |
|
| Total - Current assets |
|
|
113,115 |
|
|
|
136,384 |
|
| Non-current assets |
|
|
|
|
|
|
|
|
| Intangible assets |
|
|
48,761 |
|
|
|
46,946 |
|
| Property, plant and equipment |
|
|
7,872 |
|
|
|
8,059 |
|
| Other non-current financial assets |
|
|
4,125 |
|
|
|
3,388 |
|
| Deferred tax assets |
|
|
0 |
|
|
|
0 |
|
| Total - Non-current
assets |
|
|
60,758 |
|
|
|
58,393 |
|
| Total - Assets |
|
|
173,872 |
|
|
|
194,777 |
|
APPENDICES
Shareholders’
equity and liabilities
| |
|
As of |
| (in € thousands) |
|
|
2023/12/31 |
|
|
|
2024/06/30 |
|
| Current liabilities |
|
|
|
|
| Current convertible loans |
|
|
415 |
|
|
|
413 |
|
| Other current loans and borrowings |
|
|
7,510 |
|
|
|
7,605 |
|
| Current trade and other payables |
|
|
18,799 |
|
|
|
22,159 |
|
| Current deferred income and revenue |
|
|
11,692 |
|
|
|
6,095 |
|
| Current provisions |
|
|
40 |
|
|
|
40 |
|
| Other current tax liabilities |
|
|
23 |
|
|
|
118 |
|
| Total - Current liabilities |
|
|
38,480 |
|
|
|
36,430 |
|
| Non-current liabilities |
|
|
|
|
|
|
|
|
| Non-current convertible loans |
|
|
52,206 |
|
|
|
53,233 |
|
| Other non-current loans and borrowings |
|
|
10,047 |
|
|
|
6,553 |
|
| Non-current deferred income and revenue |
|
|
3,755 |
|
|
|
0 |
|
| Non-current employee benefits |
|
|
978 |
|
|
|
1,026 |
|
| Deferred tax liabilities |
|
|
455 |
|
|
|
171 |
|
| Total - Non-current liabilities |
|
|
67,441 |
|
|
|
60,983 |
|
| Shareholders'
equity |
|
|
|
|
|
|
|
|
| Share capital |
|
|
12,459 |
|
|
|
12,477 |
|
| Share premium |
|
|
445,261 |
|
|
|
446,490 |
|
| Retained earnings (accumulated deficit) |
|
|
(361,870 |
) |
|
|
(391,461 |
) |
| Currency translation adjustment |
|
|
996 |
|
|
|
(452 |
) |
| Net profit (loss) |
|
|
(28,894 |
) |
|
|
30,311 |
|
| Total - Shareholders'
equity |
|
|
67,951 |
|
|
|
97,363 |
|
| Total - Shareholders' equity & liabilities |
|
|
173,872 |
|
|
|
194,777 |
|
APPENDICES
Condensed
Consolidated Statement of Operations
| |
|
Half-year ended |
| (in € thousands, except earnings per share data) |
|
|
2023/06/30 |
|
|
|
2024/06/30 |
|
| |
|
|
|
|
| Revenues and
other income |
|
|
|
|
|
|
|
|
| Revenue |
|
|
11,482 |
|
|
|
58,973 |
|
| Other income |
|
|
3,893 |
|
|
|
2,226 |
|
| Revenues and other income |
|
|
15,374 |
|
|
|
61,199 |
|
| |
|
|
|
|
|
|
|
|
| Operating expenses
and other operating income (expenses) |
|
|
|
|
|
|
|
|
| Research and development expenses |
|
|
(25,630 |
) |
|
|
(18,984 |
) |
| General and administrative expenses |
|
|
(9,105 |
) |
|
|
(10,564 |
) |
| Marketing and market access expenses |
|
|
(520 |
) |
|
|
(390 |
) |
| Reorganization and restructuring income (expenses) |
|
|
633 |
|
|
|
0 |
|
| Other operating expenses |
|
|
(52 |
) |
|
|
(39 |
) |
| |
|
|
|
|
|
|
|
|
| Operating income (loss) |
|
|
(19,299 |
) |
|
|
31,222 |
|
| |
|
|
|
|
|
|
|
|
| Financial income |
|
|
1,748 |
|
|
|
1,546 |
|
| Financial expenses |
|
|
(2,890 |
) |
|
|
(2,419 |
) |
| Financial profit (loss) |
|
|
(1,141 |
) |
|
|
(873 |
) |
| |
|
|
|
|
|
|
|
|
| Net profit (loss) before
tax |
|
|
(20,440 |
) |
|
|
30,349 |
|
| |
|
|
|
|
|
|
|
|
| Income tax benefit (expense) |
|
|
(414 |
) |
|
|
(39 |
) |
| |
|
|
|
|
|
|
|
|
| Net profit (loss) |
|
|
(20,854 |
) |
|
|
30,311 |
|
| |
|
|
|
|
|
|
|
|
| Basic and diluted earnings (loss) per share |
|
|
|
|
|
|
|
|
| Basic earnings (loss) per share (€/share) |
|
|
(0.42 |
) |
|
|
0.61 |
|
| Diluted earnings (loss) per share (€/share) |
|
|
(0.42 |
) |
|
|
0.53 |
|
APPENDICES
Condensed
Statement of Cash Flows
| |
|
|
Half-year ended |
|
|
|
Half-year ended |
|
| (in € thousands) |
|
|
2023/06/30 |
|
|
|
2024/06/30 |
|
| |
|
|
|
|
| Cash flows from operating activities |
|
|
|
|
| + Net profit (loss) |
|
|
(20,854 |
) |
|
|
30,311 |
|
| |
|
|
|
|
|
|
|
|
| Reconciliation of net loss to net cash used in operating activities |
|
|
|
|
|
|
|
|
| Adjustments for: |
|
|
|
|
|
|
|
|
| + Depreciation and amortization on tangible and intangible assets |
|
|
835 |
|
|
|
854 |
|
| + Impairment and provisions |
|
|
(396 |
) |
|
|
105 |
|
| + Expenses related to share-based compensation |
|
|
274 |
|
|
|
334 |
|
| - Loss (gain) on disposal of property, plant and equipment |
|
|
(52 |
) |
|
|
(62 |
) |
| + Net finance expenses (revenue) |
|
|
763 |
|
|
|
542 |
|
| + Income tax expense (benefit) |
|
|
414 |
|
|
|
39 |
|
| + Other non-cash items |
|
|
1,199 |
|
|
|
1,687 |
|
| |
|
|
|
|
|
|
|
|
| Operating cash flows before
change in working capital |
|
|
(17,817 |
) |
|
|
33,809 |
|
| |
|
|
|
|
|
|
|
|
| Decrease (increase) in trade receivables and other assets |
|
|
(4,858 |
) |
|
|
(39,413 |
) |
| (Decrease) increase in trade payables and other liabilities |
|
|
(2,398 |
) |
|
|
(5,572 |
) |
| |
|
|
|
|
|
|
|
|
| Change in working capital |
|
|
(7,256 |
) |
|
|
(44,984 |
) |
| |
|
|
|
|
|
|
|
|
| Income tax paid |
|
|
0 |
|
|
|
(12 |
) |
| |
|
|
|
|
|
|
|
|
| Net cash flows provided
by (used in) in operating activities |
|
|
(25,074 |
) |
|
|
(11,187 |
) |
| |
|
|
|
|
|
|
|
|
| Cash flows from
investment activities |
|
|
|
|
|
|
|
|
| |
|
|
|
|
|
|
|
|
| - Acquisition net of cash acquired (Versantis intangible) |
|
|
0 |
|
|
|
0 |
|
| - Acquisition of other intangible assets |
|
|
(2,000 |
) |
|
|
0 |
|
| - Acquisition of property, plant and equipment |
|
|
61 |
|
|
|
(737 |
) |
| + Proceeds from disposal of / reimbursement of property, plant and equipment |
|
|
62 |
|
|
|
78 |
|
| - Acquisition of financial instruments |
|
|
9 |
|
|
|
(28 |
) |
| ‘+Proceeds
from disposal of financial instruments |
|
|
4,500 |
|
|
|
0 |
|
| |
|
|
|
|
|
|
|
|
| Net cash flows provided
by (used in ) investment activities |
|
|
2,682 |
|
|
|
(687 |
) |
| |
|
|
|
|
|
|
|
|
| Cash flows from
financing activities |
|
|
|
|
|
|
|
|
| |
|
|
|
|
| + Proceeds from issue of share capital (net) |
|
|
0 |
|
|
|
0 |
|
| + Proceeds from new loans and borrowings net of issue costs |
|
|
0 |
|
|
|
0 |
|
| - Repayments of loans and borrowings |
|
|
(464 |
) |
|
|
(3,143 |
) |
| - Payments on lease debts |
|
|
(530 |
) |
|
|
(545 |
) |
| - Financial interests paid (including finance lease) |
|
|
(1,106 |
) |
|
|
(1,073 |
) |
| + Financial interests received |
|
|
337 |
|
|
|
535 |
|
| |
|
|
|
|
|
|
|
|
| Net cash flows provided
by (used in ) financing activities |
|
|
(1,764 |
) |
|
|
(4,225 |
) |
| |
|
|
|
|
|
|
|
|
| Increase (decrease)
in cash and cash equivalents |
|
|
(24,155 |
) |
|
|
(16,100 |
) |
| |
|
|
|
|
|
|
|
|
| Cash and cash equivalents at the beginning of the period |
|
|
136,001 |
|
|
|
77,789 |
|
| Effects of exchange rate changes on cash |
|
|
(20 |
) |
|
|
(43 |
) |
| |
|
|
|
|
|
|
|
|
| Cash and cash
equivalents at the end of the period |
|
|
111,826 |
|
|
|
61,645 |
|
APPENDICES
| |
Discussion
of the 2024 half-year results |
|
| |
|
Comments
on the condensed statement of net income for the periods ended June 30, 2023 and June 30, 2024
|
(1) |
Revenue and other income |
The
Company’s revenue and other income mainly comprises revenue, the research tax credit, and other operating revenue.
| |
|
Half-year ended |
| (in € thousands) |
|
|
2023/06/30 |
|
|
|
2024/06/30 |
|
| Revenues |
|
|
11,482 |
|
|
|
58,973 |
|
| CIR tax credit |
|
|
3,547 |
|
|
|
2,108 |
|
| Government grants and subsidies |
|
|
82 |
|
|
|
21 |
|
| Other operating income |
|
|
263 |
|
|
|
97 |
|
| TOTAL |
|
|
15,374 |
|
|
|
61,199 |
|
For
the half-year ended June 30, 2024, total revenues and
other income amounted to €61,199, compared with €15,374 for the same period in 2023.
Revenues
For
the half-year ended June 30, 2024, revenue amounted to
€58,973 compared with €11,482 for the same period in 2023.
Revenue
is primarily composed of:
|
• |
Licensing Agreement (Ipsen). In
December 2021, GENFIT and Ipsen entered into an exclusive licensing agreement for elafibranor (marketed as Iqirvo), a Phase 3 asset evaluated
in PBC, as part of a long-term global partnership ("Collaboration and License Agreement"). |
|
– |
During the first
six months of 2024: |
|
◦ |
€48.7 million was attributable
to a milestone invoiced to Ipsen in June 2024 following the first commercial sale of Iqirvo/elafibranor in the U.S. |
|
◦ |
€9.3 million
was attributable to the partial recognition of deferred revenue as noted in Note
20 - "Deferred income and revenue". |
|
◦ |
€0.2 million was attributable
to royalty revenue from U.S. sales of Iqirvo. |
|
– |
During the first
six months of 2023: |
|
◦ |
€8.2 million
was attributable to the partial recognition of deferred revenue as noted in Note
20 - "Deferred income and revenue". |
|
• |
Transition Services Agreement (Ipsen).
GENFIT and Ipsen entered into the Transition Services Agreement and Part B Transition Services Agreement, signed in April 2022 and September
2023 respectively, in order to facilitate the transition of certain services related to the Phase 3 Elative clinical trial until the complete
transfer of the responsibility of the trial to Ipsen. |
|
– |
During the first
six months of 2024, services provided under this contract generated €0.8 million in revenue. |
|
– |
During the first
six months of 2023, services provided under this contract generated €3.2 million in revenue. |
Research
Tax Credit (CIR)
During
the first six months of 2024, the CIR amounted to €2,108 in 2024 including €177 of legally required related interest, (€3,547
for the same period in 2023), due to a reduction in eligible research and development expenses.
The
CIR receivable amounted to €7,738 as of June 30, 2024, which comprises balances from 2023 onward (compared to €12,200 for
the same period in 2023). Previously withheld balances from 2021 and 2022 have since been reimbursed
on May 28, 2024 in the amount of €6,570 which includes legally required related interest of €177.
We
were subject to a tax audit by the French tax authorities on our tax returns or operations subject to review on the 2019 and 2020 periods
(including the CIR claimed for these periods), which started on December 10, 2021 and is still ongoing at the date of this document.
Other
operating income
During
the first six months of 2024, the Group recognized €97 in “Other operating income” (€263 for the same period in
2023), mainly comprised of exchange gains on trade receivables.
|
(2) |
Operating expenses by destination |
The
tables below break operating expenses down by destination, mainly into research and development expenses, general and administrative expenses,
and marketing and market access expenses.
APPENDICES
| |
|
|
Half-year ended |
|
|
Of which : |
| |
|
|
2023/06/30 |
|
|
|
Raw |
|
|
|
Contracted |
|
|
|
Employee |
|
|
|
Other |
|
|
|
Depreciation, |
|
|
|
Gain / |
|
| |
|
|
|
|
materials |
|
|
|
research and |
|
|
|
expenses |
|
|
|
expenses |
|
|
|
amortization |
|
|
|
(loss) on |
|
| |
|
|
|
|
and |
|
|
|
development |
|
|
|
|
|
(maintenance, |
|
|
|
and |
|
|
|
disposal of |
|
| |
|
|
|
|
consumables |
|
|
|
activities |
|
|
|
|
|
fees, travel, |
|
|
|
impairment |
|
|
|
property, |
|
| |
|
|
|
|
used |
|
|
|
conducted by |
|
|
|
|
|
taxes…) |
|
|
|
charges |
|
|
|
plant and |
|
| (in € thousands) |
|
|
|
|
|
|
third parties |
|
|
|
|
|
|
|
|
|
equipment |
|
| Research and development income (expenses) |
|
|
(25,630 |
) |
|
|
(1,040 |
) |
|
|
(14,367 |
) |
|
|
(6,299 |
) |
|
|
(3,251 |
) |
|
|
(705 |
) |
|
|
33 |
|
| General and administrative expenses |
|
|
(9,105 |
) |
|
|
(162 |
) |
|
|
(96 |
) |
|
|
(3,919 |
) |
|
|
(4,645 |
) |
|
|
(283 |
) |
|
|
0 |
|
| Marketing and market access expenses |
|
|
(520 |
) |
|
|
(2 |
) |
|
|
(1 |
) |
|
|
(275 |
) |
|
|
(236 |
) |
|
|
(6 |
) |
|
|
0 |
|
| Reorganization and restructuring income (expenses) |
|
|
633 |
|
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
633 |
|
|
|
0 |
|
| Other operating income (expenses) |
|
|
(52 |
) |
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
(75 |
) |
|
|
3 |
|
|
|
20 |
|
| TOTAL |
|
|
(34,673 |
) |
|
|
(1,204 |
) |
|
|
(14,464 |
) |
|
|
(10,492 |
) |
|
|
(8,207 |
) |
|
|
(358 |
) |
|
|
52 |
|
| |
|
|
Half-year ended |
|
|
Of which : |
| |
|
|
2024/06/30 |
|
|
|
Raw |
|
|
|
Contracted |
|
|
|
Employee |
|
|
|
Other |
|
|
|
Depreciation, |
|
|
|
Gain / |
|
| |
|
|
|
|
materials |
|
|
|
research and |
|
|
|
expenses |
|
|
|
expenses |
|
|
|
amortization |
|
|
|
(loss) on |
|
| |
|
|
|
|
and |
|
|
|
development |
|
|
|
|
|
(maintenance, |
|
|
|
and |
|
|
|
disposal of |
|
| |
|
|
|
|
consumables |
|
|
|
activities |
|
|
|
|
|
fees, travel, |
|
|
|
impairment |
|
|
|
property, |
|
| |
|
|
|
|
used |
|
|
|
conducted by |
|
|
|
|
|
taxes…) |
|
|
|
charges |
|
|
|
plant and |
|
| (in € thousands) |
|
|
|
|
|
|
third parties |
|
|
|
|
|
|
|
|
|
equipment |
|
| Research and development expenses |
|
|
(18,984 |
) |
|
|
(1,056 |
) |
|
|
(7,838 |
) |
|
|
(6,610 |
) |
|
|
(2,806 |
) |
|
|
(675 |
) |
|
|
0 |
|
| General and administrative expenses |
|
|
(10,564 |
) |
|
|
(152 |
) |
|
|
(69 |
) |
|
|
(4,380 |
) |
|
|
(5,778 |
) |
|
|
(185 |
) |
|
|
0 |
|
| Marketing and market access expenses |
|
|
(390 |
) |
|
|
(2 |
) |
|
|
0 |
|
|
|
(295 |
) |
|
|
(89 |
) |
|
|
(3 |
) |
|
|
0 |
|
| Reorganization and restructuring expenses |
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
| Other operating income (expenses) |
|
|
(39 |
) |
|
|
0 |
|
|
|
0 |
|
|
|
0 |
|
|
|
(102 |
) |
|
|
0 |
|
|
|
62 |
|
| TOTAL |
|
|
(29,977 |
) |
|
|
(1,210 |
) |
|
|
(7,907 |
) |
|
|
(11,284 |
) |
|
|
(8,774 |
) |
|
|
(863 |
) |
|
|
62 |
|
For
the half-year ended June 30, 2024 operating expenses amounted to €29,977 (€34,673 for the same period in 2023).
They
include the following:
Research
and development expenses
For
the first six months of 2023, research and development expenses totaled €25.6 million. These expenses were comprised of €14.4
million in contracted research and development conducted by third parties, €6.3 million in employee expenses, €3.3 million
in other expenses, €0.7 million in depreciation, amortization and impairment charges and €1.0 million in raw materials and
consumables.
For
the first six months of 2024, research and development expenses totaled €19.0 million. These expenses were comprised of €7.8
million in contracted research and development conducted by third parties, €6.6 million in employee expenses, €2.8 million
in other expenses, €0.7 million in depreciation, amortization and impairment charges and €1.1 million in raw materials and
consumables.
The
decrease of €6.6 million in contracted research and development conducted by third parties is mainly due to:
|
• |
Decreasing
costs related to the Elative product candidate (approved by the FDA in the US in June 2024 and marketed under the name Iqirvo) of
€7.4 million, |
|
• |
Increasing
costs related to the SRT-015 product candidate of €0.5 million, and |
|
• |
Increasing
costs related to the VS-01 product candidate of €0.3 million. |
The
increase of €0.3 million in employee expenses, consisting of wages, salaries, social security, pension costs and share-based compensation
paid to employees in the research and development function, relates primarily to the increase in workforce (from 96 to 106 employees
at June 30, 2023 and 2024, respectively).
The
decrease of €0.5 million in other expenses is mainly due to decreasing costs related to maintenance costs of €0.3 million
and decreasing costs related to consultants of €0.2 million.
General
and administrative expenses
For
the first six months of 2023, general and administrative expenses totaled €9.1 million. These expenses were mainly comprised of
€3.9 million in employee expenses and €4.6 million in other expenses.
For
the first six months of 2024, general and administrative expenses totaled €10.6 million. These expenses were mainly comprised of
€4.4 million in employee expenses and €5.8 million in other expenses.
The
increase of €0.5 million in employee expenses in the general and administrative function was mainly due to the increase in workforce
(from 56 to 61 employees at June 30, 2023 and 2024, respectively).
The
increase of €1.2 million in other expenses in the general and administrative function
was mainly due to increases in i) maintenance costs of €0.7 million, ii) consulting costs of €0.2 million, iii) donations
of €0.2 million, et iv) recruiting fees of €0.1 million.
Marketing
and market access expenses
For
the first six months of 2023, marketing and market access expenses totaled €0.5 million. These expenses were mainly comprised of
€0.3 million in employee expenses and €0.2 million in other expenses.
For
the first six months of 2024, marketing and market access expenses totaled €0.4 million. These expenses were mainly comprised of
€0.3 million in employee expenses and €0.1 million in other expenses.
Marketing
and market access expenses remained stable period over period.
Reorganization
and restructuring income (expenses)
During
the first half of 2023, the Group reversed the entire remaining RESOLVE-IT® provision consisting of unused building space, which
are now in use. There was no reorganization and restructuring expense in 2024.
|
(3) |
Financial income
(expense) |
For
the half-year ended June 30, 2024, financial income amounted to a loss of €0.9 million, compared to a loss of €1.1 million
for the same period in 2023.
For
the first six months of 2024, this is primarily the result of interest expense of €2.3 million, realized and unrealized foreign
exchange loss of €0.6 million, and €1.7 million in accrued and realized interest income.
For
the first six months of 2024, this is primarily the result of interest expense of €2.3 million, realized and unrealized foreign
exchange loss of €42 thousand, and €1.3 million in accrued and realized interest income.
The
first half of 2024 resulted in net profit of €30,311 thousand compared with a net loss of €20,854 thousand in the first half
of 2023.
Comments
on the Group’s Cash Flows for the periods ended June 30, 2023 and June 30, 2024.
As
of June 30, 2024,
cash and cash equivalents amounted to €61,645.
Over
the period, change in cash flow by type of flow was as follows:
| |
|
Half-year ended |
| (in € thousands) |
|
|
2023/06/30 |
|
|
|
2024/06/30 |
|
| Cash flows provided by (used in) operating activities |
|
|
(25,074 |
) |
|
|
(11,187 |
) |
| Cash flows provided by (used in) investment activities |
|
|
2,682 |
|
|
|
(687 |
) |
| Cash flows provided by (used in) financing activities |
|
|
(1,764 |
) |
|
|
(4,225 |
) |
| |
|
|
(24,155 |
) |
|
|
(16,100 |
) |
|
(1) |
Cash flows provided by (used in) operating activities |
Cash
flow used in operating activities amounted to an outflow of €11,187 thousand for the half-year ended June 30, 2024 compared with
an outflow of €25,074 thousand for the half-year ended June 30, 2023.
In
the first half of 2024, this amount mainly stems from our research and development efforts; notably for Elative, our Phase 3 clinical
trial of elafibranor in PBC (approved by the FDA in June 2024); UNVEIL-IT®, our Phase 2 clinical trial of VS-01 in ACLF; GNS561,
as part of its cholangiocarcinoma program; and NTZ, as part of its ACLF program.
In
the first half of 2023, this amount mainly stems from our net loss of €20.9 million, which is largely the result of our research
and development efforts; notably for Elative, our Phase 3 clinical trial of elafibranor in PBC; UNVEIL-IT®, our Phase 2 clinical trial
of VS-01 in ACLF; GNS561, as part of its cholangiocarcinoma program; and NTZ, as part of its ACLF program.
The
change between the first half of 2024 and 2023 is further explained by the receipt of a milestone of €13.3 million from IPSEN in
2024 (incurred and recorded in 2023, upon the acceptance of the new drug application filing with the FDA and the filing of the marketing
authorization application with the EMA for the accelerated approval of elafibranor).
These
cash flows reflect GENFIT’s business, which requires significant research and development efforts, and generates expenses that change
in line with progress on the Company’s research programs, net of its operating revenues.
|
(2) |
Cash flows provided by (used in) investing activities |
Cash
flow used in investing activities amounted to €-687 thousand in the first half of 2024, compared with €2,682 thousand in cash
flow provided in the first half of 2023.
These
cash flows include acquisitions, disposals and repayments of fixed assets and financial assets.
|
(3) |
Cash flows provided by (used in) financing activities |
Cash
flow used in financing activities amounted to €-4,225 thousand in the first half of 2024, compared with €-1,764 thousand in
the first half of 2023.
In
the first half of 2024, these cash flows mainly reflect financial interest received and paid. The decrease is mainly explained by loan
repayments for the period.
ABOUT
GENFIT
GENFIT
is a late-stage biopharmaceutical company committed to improving the lives of patients with rare,
life-threatening liver diseases whose medical needs remain largely unmet. GENFIT is a pioneer in
liver disease research and development with a rich history and a solid scientific heritage spanning more than two decades. Today, GENFIT
has built up a diversified and rapidly expanding R&D portfolio of programs at various stages of development. The Company focuses
on Acute-on-Chronic Liver Failure (ACLF). Its ACLF franchise includes five assets under development: VS-01, NTZ, SRT-015, CLM-022 and
VS-02-HE, based on complementary mechanisms of action using different routes of administration.
Other assets target other serious diseases, such as cholangiocarcinoma (CCA), urea cycle disorder (UCD) and organic acidemia (OA). GENFIT's
expertise in the development of high-potential molecules from early to advanced stages, and in pre-commercialization, was demonstrated
with the success of the 52-week Phase 3 Elative study evaluating elafibranor in Primary Biliary Cholangitis (PBC). Elafibranor,
a 'first-in-class' molecule developed by GENFIT from initial discovery to the conclusion of a 52-week Phase 3 study, is now marketed and
commercialized in the United States by Ipsen under the trademark Iqirvo® since June 2024.
Beyond
therapies, GENFIT also has a diagnostic franchise, including NIS2+®
in Metabolic dysfunction-associated steatohepatitis (MASH,
formerly known as NASH for non-alcoholic steatohepatitis) and TS-01 focusing on blood ammonia levels. GENFIT is headquartered in
Lille, France and has offices in Paris (France), Zurich (Switzerland) and Cambridge, MA (USA). The Company is listed on the Nasdaq Global
Select Market and on the Euronext regulated market in Paris, Compartment B (Nasdaq and Euronext: GNFT). In
2021, Ipsen became one of GENFIT's largest shareholders, acquiring an 8% stake in the Company's capital. For more information,
visit www.genfit.com
FORWARD
LOOKING STATEMENTS
This
press release contains certain forward-looking statements, including those within the meaning of the Private Securities Litigation Reform
Act of 1995 with respect to GENFIT, including, but not limited to statements about GENFIT’s corporate strategy and objectives, our
ability to meet milestones and receive payments from Ipsen, the potential of Iqirvo®/elafibranor to receive marketing authorization
and successful launch and commercialization in PBC by Ipsen outside the United States, the Iqirvo®/elafibranor competitive landscape,
anticipated timing for study enrollment and data readouts and development plans for our pipeline programs, in particular for VS-01 in
ACLF and GNS561 in CCA, expected timing for potential regulatory approvals and the impact of the development of our programs, as well
as our financial outlook including cash flow and cash burn projections and business and R&D activity projections for 2024 and beyond.
The use of certain words, including “believe”, “potential,” “expect”, “target”, “may”,
“should” and “will” and similar expressions, is intended to identify forward-looking statements. Although the
Company believes its expectations are based on the current expectations and reasonable assumptions of the Company’s management,
these forward-looking statements are subject to numerous known and unknown risks and uncertainties, which could cause actual results to
differ materially from those expressed in, or implied or projected by, the forward-looking statements. These risks and uncertainties include,
among others, the uncertainties inherent in research and development, including in relation to safety of drug candidates, cost of, progression
of, and results from, our ongoing and planned clinical trials, review and approvals by regulatory authorities in the United States, Europe
and worldwide, of our drug and diagnostic candidates, potential commercial success of elafibranor if approved, exchange rate fluctuations,
and our continued ability to raise capital to fund our development, as well as those risks and uncertainties discussed or identified in
the Company’s public filings with the AMF, including those listed in Chapter 2 "Risk Factors and Internal Control" of
the Company's 2023 Universal Registration Document filed on April 5, 2024 (no. D.24-0246) with the Autorité des marchés
financiers ("AMF"), which is available on GENFIT's website (www.genfit.fr) and the AMF's website (www.amf.org), and those
discussed in the public documents and reports filed with the U.S. Securities and Exchange Commission ("SEC"), including the
Company’s 2023 Annual Report on Form 20-F filed with the SEC on April 5, 2024 and subsequent filings and reports filed with the
AMF or SEC, including the Half-Year Business and Financial Report at June 30, 2024 or otherwise made public, by the Company. In addition,
even if the results, performance, financial position and liquidity of the Company and the development of the industry in which it operates
are consistent with such forward-looking statements, they may not be predictive of results or developments in future periods. These forward-looking
statements speak only as of the date of publication of this document. Other than as required by applicable law, the Company does not undertake
any obligation to update or revise any forward-looking information or statements, whether as a result of new information, future events
or otherwise.
CONTACT
GENFIT
| Investors
Tel
: + 33 3 20 16 40 00 | investors@genfit.com
GENFIT
| Press relations
Stephanie
BOYER | Tel : + 33 3 20 16 40 00 | stephanie.boyer@genfit.com
18
Genfit (PK) (USOTC:GNFTF)
Gráfica de Acción Histórica
De Nov 2024 a Dic 2024
Genfit (PK) (USOTC:GNFTF)
Gráfica de Acción Histórica
De Dic 2023 a Dic 2024
