- TWYMEEG® sales continue to perform well in Japan with JPY
3.5 billion (EUR 22.4 million1) total sales over the first 3
quarters of 20232, up +170% vs. the corresponding period in 2022.
This growth trajectory is in line to meet or potentially surpass
Sumitomo Pharma’s FY 2023 forecast3
- The Company remains focused on securing additional financing
to execute its strategic plan in rare diseases:
- Exclusive advanced discussions with a leading investor to
monetize royalties from TWYMEEG® (Imeglimin) sales in
Japan
- Advanced discussions with several potential partners for its
three proprietary products: Imeglimin, PXL065 and PXL770
- Cost-saving plan completed end of 2023, with significant
reduction in headcount to adapt resources to the Company's current
needs
- Cash runway until March 2024, including tranches already
drawn on the equity-linked financing facility with IRIS
- As of December 31, 2023, cash and cash equivalents were EUR
2.3 million (USD 2.6 million); Poxel generated revenue of EUR 2.0
million for FY 2023
Regulatory News:
POXEL SA (Euronext: POXEL - FR0012432516), a clinical stage
biopharmaceutical company developing innovative treatments for
chronic serious diseases with metabolic pathophysiology, including
non-alcoholic steatohepatitis (NASH) and rare metabolic disorders,
today announced its cash position and revenue and provided a
corporate update for the twelve months ended December 31, 2023.
Thomas Kuhn, Chief Executive Officer of Poxel, stated:
“We remain focused and continue to concentrate all our efforts at
securing financing options, prioritizing non-dilutive solution, and
partnerships. In particular, our relentless work as well as
TWYMEEG®’s robust performance in Japan had led to the ongoing
exclusive advanced discussions with a leading investor for
monetizing royalties on TWYMEEG® sales in Japan. We’ve also
progressed our advanced discussions – in some cases on an exclusive
basis – with several potential partners for each of our three
proprietary products. Our goal is still to finalize one or more of
these financing options and/or partnerships by the end of the first
quarter of 2024 to start as soon as possible the next chapter of
Poxel in rare metabolic diseases.”
Commercial Update
TWYMEEG® (Imeglimin)
- For the quarter ended December 2023, TWYMEEG® sales in Japan
were of JPY 851 million (EUR 5.5 million)1 as reported by Sumitomo
Pharma.
- For its FY 2023, Sumitomo Pharma announced a forecast for
TWYMEEG® of JPY 4.2 billion3 (EUR 26.9 million)1, which would
represent a 90% increase over FY 2022 TWYMEEG® gross sales. Based
on this conservative assumption, Poxel expects to receive 8%
royalties on TWYMEEG® net sales. As part of the Merck Serono
licensing agreement, Poxel will pay Merck Serono a fixed 8% royalty
based on the net sales of TWYMEEG®, independent of the level of
sales.
- During Sumitomo Pharma’s FY 2024 (ending March 31, 2025), Poxel
expects TWYMEEG® net sales in Japan to reach JPY 5 billion (EUR
35.6 million)1 entitling Poxel to receive 10% royalties on all
TWYMEEG® net sales and a sales-based payment of JPY 500 million
(EUR 3.6 million)1. Beyond Sumitomo Pharma’s FY 2024, Poxel expects
to receive escalating double-digit royalties as well as additional
sales-based payments upon achievement of contractually based sales
thresholds.
- For territories not covered by its agreement with Sumitomo
Pharma, Poxel is still in advanced ongoing discussions with various
potential partners for Imeglimin.
Clinical, Manufacturing and Patent Update
TWYMEEG® (Imeglimin)
- Following the much higher increase in demand for TWYMEEG® than
expected, and temporarily tight inventories, Sumitomo Pharma
continues to work diligently to increase production to ensure
sustained inventory capacity.
- The Long-Term, 52-week, Open-label, Phase 4 Study conducted by
Sumitomo Pharma of Imeglimin in Japanese Type 2 Diabetic Patients
with Renal Impairment is currently ongoing in Japan to strengthen
TWYMEEG® profile in this key subpopulation. Top line results are
expected in 2024.
Rare metabolic diseases
- In February 2024, the European Patent Office (EPO) granted
Poxel a new patent for PXL770, a novel, proprietary direct
adenosine monophosphate kinase activator, which describes the use
of PXL770 in the treatment of Autosomal-dominant polycystic kidney
disease (ADPKD). This issued patent provides additional protection
for PXL770 through 2041, with the potential for an additional 5
years through patent term extension. End of 2023, Poxel had been
granted the same patent for PXL770 from the Japan Patent Office and
the obtention is currently under review in other territories,
including in the US.
- In adrenoleukodystrophy (ALD), PXL770 and PXL065 are prepared
to advance, subject to additional financing, into two Phase 2a
biomarker proof-of-concept (POC) clinical trials in male patients
with adrenomyeloneuropathy (AMN), the most common ALD subtype. The
studies will evaluate pharmacokinetics, safety and potential for
efficacy, following 12-week treatment, based on relevant disease
biomarkers, such as the effect on very long chain fatty acids
(VLCFA), the characteristic plasma marker of the disease.
Full-Year Cash and Revenue, ended December 31, 2023
Cash
As of December 31, 2023, total cash and cash equivalents were
EUR 2.3 million (USD 2.6 million)1, as compared to EUR 13.1 million
(USD 14.0 million) as of December 31, 2022.
EUR (in thousands)
Q4 2023
Q4 2022
Cash
2,341
13,058
Cash equivalents
-
-
Total cash and cash
equivalents*
2,341
13,058
Unaudited data.
*Net financial debt (excluding IFRS 16 impacts and derivative
debts) was 45.1 million euros at the end of Q4 2023 as compared to
EUR 29.5 million at the end of Q4 2022.
With the priority objective of relaunching its R&D
activities and executing its strategic plan in rare diseases, the
Company has focused in recent months on securing additional
financing, in particular non-dilutive solutions. In this context,
the Company entered into exclusive negotiations with a leading
investor to monetize royalties from TWYMEEG® (Imeglimin) sales in
Japan. In addition, the Company is in advanced discussions – in
some cases on an exclusive basis – with several potential partners
for each of its three products: Imeglimin, for several countries
not covered by its agreement with Sumitomo Pharma, PXL065 and
PXL770.
Poxel’s goal is to finalize one or more of these financing
options and/or partnerships by the end of the first quarter of
2024.
Pending finalization of one or more of these agreements, and in
a cautious approach given its limited financial visibility, the
Company has completed a cost-saving plan in December, which
includes a significant reduction in headcount, in order to adapt
the Company's cost structure to its current operating needs. Key
functions that enable the Company to finalize current transaction
opportunities and continue its day-to-day operations have been
retained, managing clinical, financial and business development
activities.
Based on:
- its cash position on December 31, 2023,
- the tranches already drawn4 as of the date of this press
release under the equity-linked financing facility with IRIS,
- no research and development expenses, and
- a strict control of operating expenses,
Poxel expects that its resources, including funds available to
it, will be sufficient to finance its operations and capital
expenditure requirements until March 2024, by which time the
Company expects to have completed one or more of its ongoing
operations.
Full-Year 2023 Revenue
Poxel reported revenues of EUR 2.0 million for the year ended
December 31, 2023, as compared to EUR 0.674 thousand during the
corresponding period in 2022.
Revenues for 2023 mostly reflects the JPY 313 million (EUR 2.0
million) of royalty revenue from Sumitomo Pharma, which represents
8% of TWYMEEG® net sales in Japan. Based on its current forecast,
Poxel expects to receive 8% royalties on TWYMEEG® net sales in
Japan through the Sumitomo Pharma fiscal year 2023 (April 2023 to
March 2024). As part of the Merck Serono licensing agreement, Poxel
will pay Merck Serono a fixed 8% royalty based on the net sales of
Imeglimin, independent of the level of sales.
EUR
(in thousands)
2023
Q1
3 months
2023
Q2
3 months
2023
Q3
3 months
2023
Q4
3 months
FY 2023
12 months
FY 2022
12 months
Sumitomo Pharma Agreement
449
506
664
362
1,981
673
Other
-
-
-
-
-
1
Total revenues
449
506
664
362
1,981
674
Unaudited data
Next Financial Press Release: 2023 Annual Results, on
April 09, 2024
About Poxel SA
Poxel is a clinical stage biopharmaceutical company
developing innovative treatments for chronic serious diseases
with metabolic pathophysiology, including non-alcoholic
steatohepatitis (NASH) and rare disorders. For the treatment of
NASH, PXL065 (deuterium-stabilized R-pioglitazone) met its
primary endpoint in a streamlined Phase 2 trial (DESTINY-1). In
rare diseases, development of PXL770, a first-in-class
direct adenosine monophosphate-activated protein kinase (AMPK)
activator, is focused on the treatment of adrenoleukodystrophy
(ALD) and autosomal dominant polycystic kidney disease (ADPKD).
TWYMEEG® (Imeglimin), Poxel’s first-in-class product that
targets mitochondrial dysfunction, is marketed for the treatment of
type 2 diabetes in Japan by Sumitomo Pharma and Poxel expects to
receive royalties and sales-based payments. Poxel has a strategic
partnership with Sumitomo Pharma for Imeglimin in Japan, China, and
eleven other Asian countries. Listed on Euronext Paris, Poxel is
headquartered in Lyon, France, and has subsidiaries in Boston, MA,
and Tokyo, Japan.
For more information, please visit: www.poxelpharma.com
All statements other than statements of historical fact included
in this press release about future events are subject to (i) change
without notice and (ii) factors beyond the Company’s control. These
statements may include, without limitation, any statements preceded
by, followed by or including words such as “target,” “believe,”
“expect,” “aim,” “intend,” “may,” “anticipate,” “estimate,” “plan,”
“project,” “will,” “can have,” “likely,” “should,” “would,” “could”
and other words and terms of similar meaning or the negative
thereof. Forward-looking statements are subject to inherent risks
and uncertainties beyond the Company’s control that could cause the
Company’s actual results or performance to be materially different
from the expected results or performance expressed or implied by
such forward-looking statements. The Company does not endorse or is
not otherwise responsible for the content of external hyperlinks
referred to in this press release.
Glossary
You will find below a list of words and/or expressions that are
used in this press release or in Poxel’s communication, with the
aim to bring clarification and transparency:
- Sumitomo Pharma fiscal year runs April to March. As an
example, Fiscal Year 2023 is April 1, 2023, through March 31,
2024.
- TWYMEEG® royalties: As per the Sumitomo Pharma’s
agreement, Poxel is entitled to receive royalties from the sales of
TWYMEEG® (Imeglimin) in Japan
- Sumitomo Pharma communicates gross
sales of TWYMEEG®, while TWYMEEG® royalties are calculated on
net sales.
- Net sales represent the amount of gross sales to which are
deducted potential rebates, allowances, and costs such as prepaid
freight, postage, shipping, customs duties and insurance
charges.
- Poxel is entitled to receive escalating royalties of 8-18% on
TWYMEEG® net sales from Sumitomo
Pharma.
Positive net royalties: as part of the Merck Serono
licensing agreement, Poxel will pay Merck Serono a fixed 8% royalty
based on the net sales of TWYMEEG®, independent of the level of
sales. All royalties that Poxel receives from TWYMEEG® net sales
above that 8% level are considered as positive net royalties. Net
royalties will therefore be positive for Poxel when TWYMEEG® net
sales exceed JPY 5 billion in a fiscal year and royalties reach 10%
and above.
1 Converted at the exchange rate as of December 31, 2023. 2
Sumitomo Pharma fiscal year 2023 ends March 31, 2024. 3 As per
Sumitomo Pharma FY2023 forecast of JPY 4.2 billion published on May
15, 2023. 4 Since March 31, 2023, 6 additional tranches have been
drawn for a total amount of EUR 3.3 million.
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version on businesswire.com: https://www.businesswire.com/news/home/20240215636442/en/
Contacts - Investor relations / Media
NewCap Nicolas Fossiez, Aurélie Manavarere / Arthur Rouillé
investor@poxelpharma.com +33 1 44 71 94 94
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