-- Pivotal Complete Response (CR) Data from
SELECT-MDS-1 Phase 3 Trial Expected by Mid-4Q24 --
-- Additional Data from SELECT-AML-1 Phase 2
Trial Expected in September 2024--
-- Management to Host Conference Call at 8:30
AM ET Today --
Syros Pharmaceuticals (NASDAQ: SYRS), a biopharmaceutical
company committed to advancing new standards of care for the
frontline treatment of hematologic malignancies, today reported
financial results for the quarter ended June 30, 2024 and provided
a corporate update.
“Syros is well-positioned heading into key clinical data
readouts expected in the second half of 2024, including pivotal
complete response (CR) data from the Phase 3 SELECT-MDS-1 trial by
mid-fourth quarter. In addition, we will present clinical activity
and tolerability data from over 40 patients from the SELECT-AML-1
Phase 2 trial at the SOHO 2024 annual meeting in September,” said
Conley Chee, Chief Executive Officer of Syros. “We are keenly
focused on execution across our late-stage clinical development
programs and pre-commercial activities in support of our mission to
provide tamibarotene as a new frontline standard-of-care for
patients with RARA overexpression.
“Supported by compelling, consistent clinical data generated
to-date across multiple trials, we believe our differentiated and
biologically-targeted approach with tamibarotene provides a
meaningful opportunity to address the approximately 50% of
higher-risk MDS and 30% of AML patients with RARA overexpression.
There is a significant unmet need in these two closely related
diseases, with patients and physicians looking for new, convenient,
and well-tolerated options that enhance clinical outcomes while
maintaining quality of life. As we approach two critical data
readouts, we are working diligently to prepare for our first New
Drug Application (NDA) filing and launch, so that we can
effectively deliver tamibarotene to the thousands of HR-MDS
patients in need of new treatment options. We look forward to an
exciting second half of the year and remain committed in our
pursuit to provide profound benefit to patients in need,” Mr. Chee
continued.
UPCOMING MILESTONES
- Report pivotal CR data from the SELECT-MDS-1 Phase 3 trial in
newly diagnosed HR-MDS patients with RARA gene overexpression by
the middle of the fourth quarter of 2024.
- Report clinical activity and tolerability data from a
prespecified analysis of more than 40 patients from the
SELECT-AML-1 Phase 2 trial in unfit AML patients with RARA
overexpression at the 12th Annual Meeting of the Society of
Hematologic Oncology (SOHO) meeting in September 2024.
RECENT HIGHLIGHTS
- In June, Syros hosted a webinar event to discuss disease
biology and the current treatment landscape in HR-MDS, as well as
to highlight the design of the ongoing pivotal Phase 3 SELECT-MDS-1
trial and the opportunity for tamibarotene. In addition to Syros
management, the event featured presentations from medical experts
in MDS. An archived replay of the event is available on the
Investors & Media section of Syros’ website,
www.syros.com.
Second Quarter 2024 Financial Results
- Syros did not recognize revenue in the second quarter of 2024,
as compared to $2.8 million for the second quarter of 2023. The
decrease reflects last year’s termination of Syros’ collaboration
agreement with Pfizer.
- Research and development (R&D) expenses were $22.0 million
for the second quarter of 2024, as compared to $29.6 million for
the second quarter of 2023. The decrease was primarily due to the
reduction in external R&D consulting, contract manufacturing,
and a reduction in headcount and related expenses.
- General and administrative (G&A) expenses were $5.5 million
for the second quarter of 2024, as compared to $7.2 million for the
second quarter of 2023. The decrease was primarily due to a
reduction of headcount and related expenses, consulting fees, and
facilities expenses.
- For the second quarter of 2024, Syros reported a net loss of
$23.3 million, or $0.59 per share, compared to a net loss of $36.3
million, or $1.30 per share, for the same period in 2023.
Cash and Financial Guidance
Cash, cash equivalents and marketable securities as of June 30,
2024, were $79.0 million, as compared with $108.3 million as of
March 31, 2024.
Based on its current plans, Syros believes that its existing
cash, cash equivalents and marketable securities will be sufficient
to fund its anticipated operating expenses and capital expenditure
requirements into the third quarter of 2025, beyond pivotal Phase 3
data from the SELECT-MDS-1 trial and additional data from the
randomized portion of the SELECT-AML-1 trial.
Conference Call and Webcast
Syros will host a conference call today at 8:30 a.m. ET to
discuss the second quarter 2024 financial results and provide a
corporate update.
To access the live conference call, please dial (800) 549-8228
(domestic) or (289) 819-1520 (international) and refer to
conference ID 64947. A webcast of the call will also be available
on the Investors & Media section of the Syros website at
www.syros.com. An archived replay of the webcast will be available
for approximately 30 days following the presentation.
About Syros Pharmaceuticals
Syros is committed to developing new standards of care for the
frontline treatment of patients with hematologic malignancies.
Driven by the motivation to help patients with blood disorders that
have largely eluded other targeted approaches, Syros is developing
tamibarotene, an oral selective RARα agonist in frontline patients
with higher-risk myelodysplastic syndrome and acute myeloid
leukemia with RARA gene overexpression. For more information, visit
www.syros.com and follow us on X (@SyrosPharma) and LinkedIn.
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within
the meaning of The Private Securities Litigation Reform Act of
1995, including without limitation statements regarding Syros’
clinical development plans, the progression of its clinical trials,
the timing to report clinical data, the ability to commercialize
tamibarotene and deliver benefit to patients, and the sufficiency
of Syros’ capital resources to fund its operating expenses and
capital expenditure requirements into the third quarter of 2025.
The words “anticipate,” “believe,” “continue,” “could,” “estimate,”
“expect,” “hope,” “intend,” “may,” “plan,” “potential,” “predict,”
“project,” “target,” “should,” “would,” and similar expressions are
intended to identify forward-looking statements, although not all
forward-looking statements contain these identifying words. Actual
results or events could differ materially from the plans,
intentions and expectations disclosed in these forward-looking
statements as a result of various important factors, including
Syros’ ability to: advance the development of its programs under
the timelines it projects in current and future clinical trials;
demonstrate in any current and future clinical trials the requisite
safety, efficacy and combinability of its drug candidates; sustain
the response rates and durability of response seen to date with its
drug candidates; successfully develop a diagnostic test to identify
patients with the RARA biomarker; obtain and maintain patent
protection for its drug candidates and the freedom to operate under
third party intellectual property; obtain and maintain necessary
regulatory approvals; identify, enter into and maintain
collaboration agreements with third parties; manage competition;
manage expenses; raise the substantial additional capital needed to
achieve its business objectives; attract and retain qualified
personnel; and successfully execute on its business strategies;
risks described under the caption “Risk Factors” in Syros’ Annual
Report on Form 10-K for the year ended December 31, 2023 and
Quarterly Report on Form 10-Q for the quarter ended June 30, 2024,
each of which is on file with the Securities and Exchange
Commission; and risks described in other filings that Syros makes
with the Securities and Exchange Commission in the future.
Financial Tables
Syros Pharmaceuticals,
Inc.
Selected Condensed
Consolidated Balance Sheet Data
(in thousands)
(unaudited)
June 30, 2024
December 31, 2023
Cash, cash equivalents and marketable
securities (current and noncurrent)
$
78,964
$
139,526
Working capital1
60,400
108,299
Total assets
106,722
168,174
Total stockholders’ (deficit) equity
(6,352)
16,662
(1)
The Company defines working capital as
current assets less current liabilities. See the Company’s
condensed consolidated financial statements for further details
regarding its current assets and current liabilities.
Syros Pharmaceuticals,
Inc.
Condensed Consolidated
Statement of Operations
(in thousands, except share
and per share data)
(unaudited)
Three Months Ended
Six Months Ended
June 30,
June 30,
2024
2023
2024
2023
Revenue
$
—
$
2,833
$
—
$
5,787
Operating expenses:
Research and development
21,953
29,608
46,608
58,369
General and administrative
5,463
7,225
11,729
14,630
Total operating expenses
27,416
36,833
58,337
72,999
Loss from operations
(27,416
)
(34,000
)
(58,337
)
(67,212
)
Interest income
1,085
2,125
2,631
3,900
Interest expense
(1,382
)
(1,278
)
(2,689
)
(2,495
)
Change in fair value of warrant
liabilities
4,386
(3,105
)
31,360
5,760
Net loss applicable to common
stockholders
$
(23,327
)
$
(36,258
)
$
(27,035
)
$
(60,047
)
Net loss per share applicable to common
stockholders - basic and diluted
$
(0.59
)
$
(1.30
)
$
(0.69
)
$
(2.15
)
Weighted-average number of common shares
used in net loss per share applicable to common stockholders -
basic and diluted
39,269,434
27,913,448
39,123,740
27,878,030
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240731944527/en/
Syros Contact Karen Hunady Director of Corporate
Communications & Investor Relations 1-857-327-7321
khunady@syros.com
Investor Relations Amanda Isacoff Precision AQ
1-212-362-1200 amanda.isacoff@precisionaq.com
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