Zymeworks Inc. (Nasdaq: ZYME), a clinical-stage biotechnology
company developing a diverse pipeline of novel, multifunctional
biotherapeutics to improve the standard of care for
difficult-to-treat diseases, today reported financial results for
the three months ended March 31, 2024 and provided a summary
of recent business highlights.
“We are very pleased to have presented five poster
presentations at AACR, which showcase Zymeworks’ ability to apply
key insights from our proprietary technology and in-house expertise
to optimize our product development candidates for targets of
significant interest,” said Kenneth Galbraith, Chair and Chief
Executive Officer of Zymeworks. “As we prepare to enter multiple
Phase 1 trials in the coming 24 months, our commitment to advancing
innovative solutions remains evident, with more preclinical data
for our early-stage pipeline to be presented throughout 2024.”
Mr. Galbraith continued, “Consistent with our
previous disclosures, our anticipated cash runway remains on track
to support the development of our 5 by 5 product pipeline into the
second half of 2027. While we approach milestones that may result
in further extension of this runway, we remain diligent in
efficiently managing our operating expenses as we continue to
execute on the strategic clinical development plans for our
assets.”
Recent Highlights and Current
Developments
Zanidatamab Continues to Progress with Promising
Developments
- In March 2024, our partner Jazz
announced their intention to initiate a Phase 3 clinical trial,
EMPOWHER, in the second half of 2024 to evaluate zanidatamab plus
chemotherapy or trastuzumab plus chemotherapy in patients with
HER2-positive breast cancer whose disease has progressed on
previous T-DXd treatment.
- In April 2024, our
partner Jazz announced the completion of the rolling BLA submission
to the FDA seeking accelerated approval for zanidatamab as a
treatment for previously-treated, unresectable locally advanced, or
metastatic HER2-positive BTC.
- In April 2024, our partner Jazz
announced their participation at the 2024 ASCO annual meeting with
an abstract for zanidatamab in BTC to be included in a poster
session, titled “Zanidatamab in previously-treated HER2+ BTC: OS
and longer follow-up from the phase 2b HERIZON-BTC-01 study”.
- In May 2024, our partner Jazz guided
that their plans to submit a marketing authorization application
(MAA) to the European Medicines Agency (EMA) for zanidatamab in BTC
are proceeding.
Progression of Research & Development
Programs
-
Presentation of five posters at the AACR Annual Meeting in April.
Posters included two presentations from our multispecific antibody
therapeutics (MSAT) program:
-
DLL3 TriTCE Co-Stim: A next generation trispecific T cell engager
with integrated CD28 costimulation for the treatment of
DLL3-expressing cancers (Abstract #6716)
-
TriTCE Co-Stim: A next generation trispecific T cell engager
platform with integrated CD28 costimulation, engineered to improve
responses in the treatment of solid tumors (Abstract #6719)
and three posters from our
antibody-drug conjugate (ADC) program:
-
-
ZW191 - a FRα-targeting antibody-drug conjugate with strong
preclinical activity across multiple FRα-expressing indications
(Abstract #1862)
-
Screening novel format antibodies to design bispecific ADCs that
address target heterogeneity (Abstract #2052)
-
Development of three-dimensional cancer cell line spheroid models
for the in vitro functional characterization of cytotoxic
antibody-drug conjugates (Abstract #3127)
- On
track to submit two IND and foreign equivalent submissions for
ZW191 and ZW171 in 2024 to commence recruitment in Phase 1 clinical
studies.
“We’re pleased to have multiple opportunities in
2024 to present our unique development approach, which we believe
places Zymeworks as a thought leader in the antibody-drug conjugate
and multispecific antibody space. Our R&D efforts are focused
on attractive targets, with the ability to use our proprietary
technology to develop next generation candidates with the potential
to advance new modalities that we have not previously seen in
oncology, and beyond,” stated Paul Moore, Ph.D., Chief Scientific
Officer at Zymeworks. “We look forward to showcasing how this
technology and in-house expertise could be used to develop
candidates in other therapeutic areas such as blood cancers and
autoimmune and inflammatory diseases.”
Board of Directors Addition
- On March 28, 2024,
Zymeworks announced the appointment of Dr. Neil Gallagher to its
board of directors, effective April 2, 2024. Dr. Gallagher was also
appointed to serve as a member of the research and development
committee of the board of directors. Dr. Gallagher is the sixth new
director elected or appointed to the Board in the past 12
months.
Financial Results for the
Three Months Ended March 31,
2024
Revenue was $10.0 million for the three months
ended March 31, 2024 compared to $35.6 million for the same
period in 2023. Revenue for the three months ended March 31,
2024 included $9.9 million for development support and drug supply
revenue from Jazz and $0.2 million from our partners for research
support and other payments. Revenue for the same period in 2023
included $34.4 million revenue for development support and drug
supply payments from Jazz and $1.2 million from our partners for
research support and other payments. The decrease in revenue from
Jazz reflects the transfer of responsibility for certain clinical
trials regarding zanidatamab to Jazz pursuant to a stock and asset
purchase agreement with Jazz (as amended, the Transfer Agreement)
and a collaboration agreement with Jazz (as amended, the Amended
Collaboration Agreement), with such future costs to be borne by
Jazz instead of being incurred by us and reimbursed by Jazz.
Research and development expense was $32.0 million
for the three months ended March 31, 2024 compared to $45.9
million for the same period in 2023. The decrease in research and
development expense was primarily due to a decrease in expenses for
zanidatamab as a result of transfer of responsibility for this
program to Jazz per our Transfer Agreement and the Amended Jazz
Collaboration Agreement. This decrease, compared to the same period
in 2023, was partially offset by an increase in preclinical
expenses, primarily with respect to preclinical product candidates
ZW171, ZW191 and ZW220. Salaries and benefits expenses decreased
compared to the same period in 2023, due to lower headcount in
2024, which was partially offset by an increase in stock-based
compensation expense in 2024.
General and administrative expense was $15.8
million for the three months ended March 31, 2024 compared to
$16.9 million for the same period in 2023. The decrease in general
and administrative expense was primarily due to a decrease in
expenses related to external legal spend and insurance expenses
compared to the same period in 2023.
Other income, net increased by $1.9 million
for the three months ended March 31, 2024 compared to the same
period in 2023. Other income, net for 2024 included $5.9 million in
interest income and $0.3 million in net foreign exchange gain and
other miscellaneous income. Other income, net for the three months
ended March 31, 2023 included $4.8 million in interest income
and a $0.5 million net foreign exchange loss and other
miscellaneous amounts. The increase in interest income was driven
by higher rates of return on our cash, cash equivalents and
marketable securities.
Income tax expense decreased by $1.3 million for
the three months ended March 31, 2024 compared to the same
period in 2023, primarily due to a reduction in U.S. taxes under
the global intangible low-taxed income rules for the three months
ended March 31, 2024.
Net loss for the three months ended March 31,
2024 was $31.7 million compared to $24.4 million loss for the same
period in 2023. The increase in net loss was due to decrease in
revenue, which was partially offset by a decrease in operating
expenses and an increase in interest income. As of March 31,
2024, we had $420.5 million of cash resources consisting of cash,
cash equivalents and marketable securities, comprised of $114.8
million in cash and cash equivalents and $305.7 million in
marketable securities. Based on current operating plans and receipt
of certain anticipated regulatory milestones, we expect our
existing cash resources as of March 31, 2024, when combined
with certain anticipated regulatory milestone payments, will enable
us to fund planned operations into the second half of
2027.
About Zymeworks Inc.
Zymeworks is a global biotechnology company
committed to the discovery, development, and commercialization of
novel, multifunctional biotherapeutics. Zymeworks’ mission is to
make a meaningful difference in the lives of people impacted by
difficult-to-treat cancers and other diseases. The Company’s
complementary therapeutic platforms and fully integrated drug
development engine provide the flexibility and compatibility to
precisely engineer and develop highly differentiated antibody-based
therapeutic candidates. Zymeworks engineered and developed
zanidatamab, a HER2-targeted bispecific antibody using the
Company’s proprietary Azymetric™ technology. Zymeworks has entered
into separate agreements with BeiGene, Ltd. (BeiGene) and Jazz
Pharmaceuticals Ireland Limited (Jazz), granting each exclusive
rights to develop and commercialize zanidatamab in different
territories. Zanidatamab is currently being evaluated in multiple
global clinical trials as a potential best-in-class treatment for
patients with HER2-expressing cancers. A Biologics License
Application (BLA) to the U.S. Food and Drug Administration (FDA)
seeking accelerated approval for the HER2-targeted bispecific
antibody zanidatamab as a treatment for previously treated,
unresectable, locally advanced, or metastatic HER2-positive biliary
tract cancer (BTC) has been submitted by Zymeworks’ partner, Jazz.
If approved, zanidatamab would be the first HER2-targeted treatment
specifically approved for BTC in the United States. Zymeworks is
rapidly advancing a deep pipeline of product candidates based on
its experience and capabilities in both antibody drug conjugates
and multispecific antibody therapeutics across multiple novel
targets in indications that represent areas of significant unmet
medical need. In addition to Zymeworks’ wholly owned pipeline, its
therapeutic platforms have been further leveraged through strategic
partnerships with global biopharmaceutical companies. For
information about Zymeworks, visit www.zymeworks.com and follow
@ZymeworksInc on X.
Cautionary Note Regarding Forward-Looking
Statements
This press release includes “forward-looking
statements” or information within the meaning of the applicable
securities legislation, including Section 27A of the Securities Act
of 1933, as amended, and Section 21E of the Securities Exchange Act
of 1934, as amended. Forward-looking statements in this press
release include, but are not limited to, statements that relate to
Zymeworks’ expectations regarding implementation of its strategic
priorities; the anticipated benefits of the collaboration agreement
with Jazz, including Zymeworks’ ability to receive any future
milestone payments and royalties thereunder; the potential
addressable market of zanidatamab; the timing of and results of
interactions with regulators; Zymeworks’ clinical development of
its product candidates and enrollment in its clinical trials; the
timing and status of ongoing and future studies and the related
data; anticipated preclinical and clinical data presentations;
expectations regarding future regulatory filings and approvals and
the timing thereof; the timing of and results of interactions with
regulators; potential safety profile and therapeutic effects of
zanidatamab and Zymeworks’ other product candidates; expected
financial performance and future financial position; the commercial
potential of technology platforms and product candidates; our
ability to satisfy potential regulatory and commercial milestones
with existing and future partners; the timing and status of ongoing
and future studies and the release of data; anticipated continued
receipt of revenue from existing and future partners; Zymeworks’
preclinical pipeline; anticipated sufficiency of existing cash
resources and certain anticipated regulatory milestone payments to
fund Zymeworks’ planned operations into the second half of 2027;
Zymeworks’ ability to execute new collaborations and partnerships
and other information that is not historical information. When used
herein, words such as “plan”, “believe”, “expect”, “may”,
“continue”, “anticipate”, “potential”, “will”, “progress”, and
similar expressions are intended to identify forward-looking
statements. In addition, any statements or information that refer
to expectations, beliefs, plans, projections, objectives,
performance or other characterizations of future events or
circumstances, including any underlying assumptions, are
forward-looking. All forward-looking statements are based upon
Zymeworks’ current expectations and various assumptions. Zymeworks
believes there is a reasonable basis for its expectations and
beliefs, but they are inherently uncertain. Zymeworks may not
realize its expectations, and its beliefs may not prove correct.
Actual results could differ materially from those described or
implied by such forward-looking statements as a result of various
factors, including, without limitation: any of Zymeworks’ or its
partners’ product candidates may fail in development, may not
receive required regulatory approvals, or may be delayed to a point
where they are not commercially viable; Zymeworks may not achieve
milestones or receive additional payments under its collaborations;
regulatory agencies may impose additional requirements or delay the
initiation of clinical trials; the impact of new or changing laws
and regulations; market conditions; the impact of pandemics and
other health crises on Zymeworks’ business, research and clinical
development plans and timelines and results of operations,
including impact on its clinical trial sites, collaborators, and
contractors who act for or on Zymeworks’ behalf; clinical trials
may not demonstrate safety and efficacy of any of Zymeworks’ or its
collaborators’ product candidates; Zymeworks’ assumptions and
estimates regarding its financial condition, future financial
performance and estimated cash runway may be incorrect; inability
to maintain or enter into new partnerships or strategic
collaborations; and the factors described under “Risk Factors” in
Zymeworks’ quarterly and annual reports filed with the Securities
and Exchange Commission (copies of which may be obtained at
www.sec.gov and www.sedar.com).
Although Zymeworks believes that such
forward-looking statements are reasonable, there can be no
assurance they will prove to be correct. Investors should not place
undue reliance on forward-looking statements. The above
assumptions, risks and uncertainties are not exhaustive.
Forward-looking statements are made as of the date hereof and,
except as may be required by law, Zymeworks undertakes no
obligation to update, republish, or revise any forward-looking
statements to reflect new information, future events or
circumstances, or to reflect the occurrences of unanticipated
events.
ZYMEWORKS INC. Condensed
Interim Consolidated Statements of Loss and Comprehensive
Loss (Expressed in thousands of U.S. dollars
except share and per share data) (unaudited)
|
Three Months Ended March 31, |
|
|
2024 |
|
|
|
2023 |
|
Revenue |
|
|
|
Research and development collaborations |
$ |
10,030 |
|
|
$ |
35,578 |
|
Operating expenses: |
|
|
|
Research and development |
|
32,042 |
|
|
|
45,912 |
|
General and administrative |
|
15,790 |
|
|
|
16,947 |
|
Total operating expenses |
|
47,832 |
|
|
|
62,859 |
|
Loss from operations |
|
(37,802 |
) |
|
|
(27,281 |
) |
Other income, net |
|
6,224 |
|
|
|
4,318 |
|
Loss before income taxes |
|
(31,578 |
) |
|
|
(22,963 |
) |
Income tax expense |
|
(75 |
) |
|
|
(1,390 |
) |
Net loss |
$ |
(31,653 |
) |
|
$ |
(24,353 |
) |
Other comprehensive (loss) income: |
|
|
|
Unrealized (loss) income on available for sale securities, net of
tax of nil |
|
(1,121 |
) |
|
|
720 |
|
Total other comprehensive (loss) income |
|
(1,121 |
) |
|
|
720 |
|
Comprehensive loss |
$ |
(32,774 |
) |
|
$ |
(23,633 |
) |
|
|
|
|
Net loss per common share: |
|
|
|
Basic |
$ |
(0.42 |
) |
|
$ |
(0.36 |
) |
Diluted |
$ |
(0.42 |
) |
|
$ |
(0.37 |
) |
Weighted-average common stock outstanding: |
|
|
|
Basic |
|
76,214,833 |
|
|
|
66,739,308 |
|
Diluted |
|
76,248,158 |
|
|
|
66,742,030 |
|
|
|
|
|
|
|
|
|
ZYMEWORKS INC.Condensed
Consolidated Balance Sheet(Expressed in thousands
of U.S. dollars) (unaudited)
|
|
|
|
|
March 31,2024 |
|
December 31,2023 |
|
|
|
|
Assets |
|
|
|
Current assets: |
|
|
|
Cash, cash equivalents and short-term marketable securities |
$ |
345,047 |
|
$ |
374,327 |
Accounts receivable |
|
30,949 |
|
|
19,477 |
Other current assets |
|
17,824 |
|
|
19,122 |
Long-term marketable securities |
|
75,446 |
|
|
81,930 |
Other long-term assets |
|
84,486 |
|
|
86,024 |
Total assets |
$ |
553,752 |
|
$ |
580,880 |
|
|
|
|
Liabilities |
|
|
|
Current liabilities: |
|
|
|
Accounts payable and accrued expenses |
$ |
47,434 |
|
$ |
45,992 |
Other current liabilities |
|
9,456 |
|
|
9,771 |
Long-term liabilities |
|
58,863 |
|
|
60,311 |
Total liabilities |
|
115,753 |
|
|
116,074 |
Stockholders’ equity |
|
437,999 |
|
|
464,806 |
Total liabilities and stockholders’ equity |
$ |
553,752 |
|
$ |
580,880 |
Contacts:
Investor Inquiries:Shrinal InamdarDirector,
Investor Relations(604) 678-1388 ir@zymeworks.com
Media Inquiries: Diana PapoveSenior Director,
Corporate Communications(604) 678-1388 media@zymeworks.com
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