Structure Therapeutics Inc. (NASDAQ: GPCR), a clinical-stage global
biopharmaceutical company developing novel oral small molecule
therapeutics for metabolic diseases, today reported financial
results for the fourth quarter and full year ended December 31,
2024, and provided a business update.
“In 2024, we made significant advancements in our oral small
molecule obesity portfolio delivering positive data for
aleniglipron and selecting our first-in-class oral small molecule
amylin receptor agonist. We completed a $547 million financing
putting us in a strong financial position,” said Raymond Stevens,
Ph.D., Founder and CEO of Structure Therapeutics. “We believe 2025
will be a transformative year for all oral selective GLP-1 small
molecules in obesity and related diseases to address making these
medicines more accessible to all. Structure Therapeutics is
well-positioned as a leader with aleniglipron as the second most
advanced oral GLP-1 small molecule with 36-week data by year-end
and a potential best-in-class profile that is combinable with other
medicines.”
“Our top priority is execution of ACCESS and ACCESS II clinical
studies, and we’re excited to announce the completion of enrollment
in both studies, which speaks to investigator and patient
enthusiasm for aleniglipron. In addition, our oral amylin receptor
agonist candidate, ACCG-2671, is expected to begin Phase 1
development by year-end, giving us two oral small molecule backbone
therapies for obesity with a robust pipeline of potential
combination therapies currently being investigated,” said Blai
Coll, M.D., Ph.D., Chief Medical Officer of Structure
Therapeutics.
Recent and Upcoming
MilestonesAleniglipron (GSBR-1290) – Oral Small
Molecule Selective GLP-1R Agonist for Obesity
- Enrollment in both the ACCESS and ACCESS II studies, totaling
over 300 patients, has been completed on schedule and topline
36-week data from both studies are expected by year-end 2025.
- ACCESS enrolled approximately 220 adults living with obesity,
or overweight with a weight-related comorbidity, and is designed to
evaluate doses up to 120 mg of aleniglipron with an optimized
4-week titration regiment.
- ACCESS II enrolled approximately 80 adults living with obesity,
or overweight with a weight-related comorbidity, and is designed to
evaluate higher doses of aleniglipron (180 mg and 240 mg) with
optimized 4-week titration increments.
ACCG-2671 – Oral Small Molecule Amylin Receptor Agonist
for Obesity
- In December 2024, Structure Therapeutics announced the
selection of ACCG-2671 as its first development candidate and has
commenced IND-enabling activities.
- ACCG-2671’s preclinical profile exhibited robust in vivo
efficacy and a pharmacokinetic and safety profile supporting
once-daily oral dosing in humans.
- Structure Therapeutics plans to initiate Phase 1 clinical study
by year-end 2025.
Oral Small Molecule Obesity Pipeline:
- Oral Small Molecule GIPR Program: Structure Therapeutics is
developing a GIPR selective agonist and antagonist and GLP-1R/GIPR
combinations to treat obesity and associated diseases.
- Oral Small Molecule GCGR Program: Structure Therapeutics is
developing a GCGR selective agonist and GLP-1R/GCGR combinations
for the treatment of obesity and related diseases.
- Oral Small Molecule APJR Program: Structure Therapeutics is
evaluating ANPA-0073, a Phase 2 ready biased APJR agonist for
potential selective or muscle-sparing weight loss. The Company has
completed a Phase 1 single-ascending and multiple-ascending dose
study, in which ANPA-0073 was generally well-tolerated with no
serious adverse events reported. Long term chronic GLP-toxicology
studies are currently underway and expected to be completed in
2025.
Fourth Quarter and Full Year 2024 Financial
Highlights
Cash Position: Cash, cash equivalents and short-term
investments totaled $883.5 million on December 31, 2024. The
Company expects its current cash, cash equivalents and short-term
investments to fund projected operations and key clinical
milestones through at least 2027, including aleniglipron studies
for Phase 3 readiness but excluding Phase 3 registrational
studies.
Research and Development (R&D) Expenses: R&D
expenses for the fourth quarter of 2024 were $33.5 million, as
compared to $20.0 million for the same period in 2023. For the year
ended December 31, 2024, R&D expenses were $108.8 million, as
compared to $70.1 million for the full year 2023. The increase was
primarily due to increases in personnel-related expenses due to an
increase in headcount, an increase in research and development
expenses and consulting services to support the advancement of our
GLP-1R franchise including aleniglipron and an increase in the
allocation of facilities costs.
General and Administrative (G&A) Expenses: G&A
expenses for the fourth quarter of 2024 were $13.6 million, as
compared to $11.0 million for the same period in 2023. For the year
ended December 31, 2024, G&A expenses were $49.4 million, as
compared to $32.7 million for the full year 2023. The increase was
primarily due to increases in personnel-related expenses and
professional services as we expanded our infrastructure to drive
and support the growth in our operations as a publicly-traded
company.
Net Loss: Net loss for the fourth quarter of 2024 totaled
$36.5 million, with non-cash share-based compensation expense of
$5.8 million, compared to $24.5 million for the fourth quarter of
2023 with non-cash share-based compensation expense of $1.9
million. For the year ended December 31, 2024, net loss totaled
$122.5 million, with non-cash share-based compensation expense of
$18.8 million, compared to $89.6 million for the full year 2023
with non-cash share-based compensation expense of $8.2 million.
About Structure TherapeuticsStructure
Therapeutics is a science-driven clinical-stage biopharmaceutical
company focused on discovering and developing innovative oral small
molecule treatments for chronic metabolic and cardiopulmonary
conditions with significant unmet medical needs. Utilizing its next
generation structure-based drug discovery platform, the Company has
established a robust GPCR-targeted pipeline, featuring multiple
wholly-owned proprietary clinical-stage oral small molecule
compounds designed to surpass the manufacturing scalability
limitations of traditional biologic and peptide therapies and be
accessible to more patients around the world. For additional
information, please visit www.structuretx.com.
Forward Looking Statements This press release
contains “forward-looking statements” within the meaning of the
“safe harbor” provisions of the Private Securities Litigation
Reform Act of 1995. All statements other than statements of
historical fact are statements that could be deemed forward-looking
statements, including, without limitation, statements concerning:
the Company’s future plans and prospects; the Company’s anticipated
cash runway and uses of cash; the belief that 2025 will be a
transformative year for all oral selective GLP-1 small molecules in
obesity; the expectation that aleniglipron has a potential
best-in-class profile that is combinable with other medicines; any
expectations regarding the safety, efficacy or tolerability of
aleniglipron, ACCG-2671, ANPA-0073 and other candidates under
development; the ability of aleniglipron, ACCG-2671, ANPA-0073 to
treat obesity, weight loss, Type 2 diabetes or related indications,
as applicable; the planned initiation of the Phase 1 clinical study
of ACCG-2671 and the timing thereof; the selection of a development
candidate for the Company’s GIPR and GLP-1R/GIPR programs; the
potential for ACCG-2761 to be a first-in-class oral small molecule
amylin agonist; the potential applications of ANPA-0073; and the
planned timing of the Company’s data results. In addition, when or
if used in this press release, the words and phrases “expect,” “on
track,” “plan,” “potential,” “promising,” “to be,” and similar
expressions and their variants, as they relate to the Company may
identify forward-looking statements. Forward-looking statements are
neither historical facts nor assurances of future performance.
Although the Company believes the expectations reflected in such
forward-looking statements are reasonable, the Company can give no
assurance that such expectations will prove to be correct. Readers
are cautioned that actual results, levels of activity, safety,
performance or events and circumstances could differ materially
from those expressed or implied in the Company’s forward-looking
statements due to a variety of risks and uncertainties, which
include, without limitation, risks and uncertainties related to the
results from earlier clinical studies not necessarily being
predictive of future results, potential delays in the commencement,
enrollment and completion of the Company’s planned clinical
studies, the Company’s ability to advance aleniglipron, ACCG-2671,
ANPA-0073, LTSE-2578, and its other therapeutic candidates, obtain
regulatory approval of and ultimately commercialize the Company’s
therapeutic candidates, competitive products or approaches limiting
the commercial value of the Company’s product candidates, the
timing and results of preclinical and clinical studies, the
Company’s ability to fund development activities and achieve
development goals, the Company's reliance on third parties,
including clinical research organizations, manufacturers, suppliers
and collaborators, over which it may not always have full control,
the impact of any global pandemics, inflation, tariffs, supply
chain issues, rising interest rates, future bank failures and other
macroeconomic factors on the Company’s business, its ability to
protect its intellectual property and other risks and
uncertainties described in the Company’s filings with the
Securities and Exchange Commission (SEC), including the Company’s
latest Annual Report on Form 10-K and future reports the Company
may file with the SEC from time to time. All forward-looking
statements contained in this press release speak only as of the
date on which they were made and are based on management’s
assumptions and estimates as of such date. The Company undertakes
no obligation to update such statements to reflect events that
occur or circumstances that exist after the date on which they were
made, except as required by law.
STRUCTURE
THERAPEUTICS INC. |
Condensed
Consolidated Statements of Operations |
(unaudited) |
(In thousands) |
|
|
THREE MONTHS
ENDED |
|
YEAR
ENDED |
|
DECEMBER 31, |
|
DECEMBER 31, |
|
2024 |
|
2023 |
|
2024 |
|
2023 |
Operating
expenses: |
|
|
|
|
|
|
|
|
|
|
|
Research and development |
$ |
33,487 |
|
|
$ |
20,042 |
|
|
$ |
108,814 |
|
|
$ |
70,103 |
|
General and administrative |
|
13,574 |
|
|
|
10,952 |
|
|
|
49,414 |
|
|
|
32,672 |
|
Total
operating expenses |
|
47,061 |
|
|
|
30,994 |
|
|
|
158,228 |
|
|
|
102,775 |
|
Loss from
operations |
|
(47,061 |
) |
|
|
(30,994 |
) |
|
|
(158,228 |
) |
|
|
(102,775 |
) |
Interest and
other income, net |
|
10,718 |
|
|
|
6,179 |
|
|
|
36,012 |
|
|
|
13,391 |
|
Loss before
provision for income taxes |
|
(36,343 |
) |
|
|
(24,815 |
) |
|
|
(122,216 |
) |
|
|
(89,384 |
) |
Provision
for (benefit from) income taxes |
|
136 |
|
|
|
(312 |
) |
|
|
310 |
|
|
|
236 |
|
Net
loss |
$ |
(36,479 |
) |
|
$ |
(24,503 |
) |
|
$ |
(122,526 |
) |
|
$ |
(89,620 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
STRUCTURE
THERAPEUTICS INC. |
Condensed
Consolidated Balance Sheet Data |
(unaudited) |
(In thousands) |
|
|
|
|
|
|
|
DECEMBER 31, |
|
2024 |
|
2023 |
Assets |
|
|
|
|
|
Current
assets: |
|
|
|
|
|
Cash, cash equivalents and short-term investments |
$ |
883,518 |
|
$ |
467,323 |
Prepaid expenses and other current assets |
|
7,693 |
|
|
6,285 |
Total current assets |
|
891,211 |
|
|
473,608 |
Property and equipment, net |
|
3,478 |
|
|
3,228 |
Operating right-of-use assets |
|
3,535 |
|
|
5,136 |
Other non-current assets |
|
5,106 |
|
|
45 |
Total assets |
$ |
903,330 |
|
$ |
482,017 |
Liabilities and shareholders’ equity |
|
|
|
|
|
Current
liabilities: |
|
|
|
|
|
Accounts payable |
$ |
8,024 |
|
$ |
4,742 |
Accrued expenses and other current liabilities |
|
26,299 |
|
|
18,558 |
Operating lease liabilities, current portion |
|
1,698 |
|
|
1,440 |
Total current liabilities |
|
36,021 |
|
|
24,740 |
Operating lease liabilities, net of current portion |
|
2,164 |
|
|
4,013 |
Other non-current liabilities |
|
302 |
|
|
298 |
Total liabilities |
|
38,487 |
|
|
29,051 |
Total shareholders’ equity |
|
864,843 |
|
|
452,966 |
Total liabilities and shareholders’ equity |
$ |
903,330 |
|
$ |
482,017 |
|
|
|
|
|
|
Investors:Danielle KeatleyStructure
Therapeutics Inc.ir@structuretx.com
Media:Dan Budwick1ABDan@1abmedia.com
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