Scholar Rock Reports Third Quarter 2022 Financial Results and Highlights Business Progress
Scholar Rock (SRRK) reported its Q3 2022 financial results, revealing a net loss of $43.3 million or $0.55 per share, compared to a net loss of $37.5 million or $1.02 per share in Q3 2021. Revenue fell to $0 from $5.5 million in the previous year. Notable updates include positive 24-month TOPAZ trial data for apitegromab in spinal muscular atrophy and ongoing enrollment for the Phase 3 SAPPHIRE trial. The company amended its debt facility, adding $25 million in capacity and extending loan terms. Cash reserves stand at $343.7 million, expected to fund operations into 2025.
- Presented positive 24-month quality-of-life data from TOPAZ trial for apitegromab.
- Ongoing enrollment in the SAPPHIRE trial shows strong clinical momentum.
- Cash reserves of $343.7 million will fund operations through 2025.
- Net loss increased to $43.3 million in Q3 2022, up from $37.5 million in Q3 2021.
- Revenue dropped to $0 from $5.5 million year-over-year.
- Presented 24-month apitegromab data on quality-of life-measures from the TOPAZ trial and SRK-181 data from DRAGON trial at major medical/scientific congresses
- Announced key leadership appointments
- Amended existing debt facility with Oxford finance and
"We continue to build conviction in our clinical programs with recent TOPAZ data indicating apitegromab’s potential for sustained improvements of quality-of-life measures over 24 months, and with the most recently available SRK-181 data from DRAGON that we presented at SITC,” said
Company Highlights and Upcoming Milestones
Pipeline Updates
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Apitegromab is a selective inhibitor of myostatin activation being developed as the potential first muscle-targeted therapy for the treatment of spinal muscular atrophy (SMA).
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Presented new Phase 2 TOPAZ trial data indicating positive trends in quality-of-life measures over 24 months with apitegromab for nonambulatory patients with Types 2 and 3 SMA.
Scholar Rock presented these data, which indicate the potential for sustained improvement in quality-of-life measures for patients with symptomatic SMA and offer further signs of possible durable effects of apitegromab, at theWorld Muscle Society (WMS) Hybrid Congress and theInternational Scientific Congress on Spinal Muscular Atrophy in October.
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Continued enrollment of the Phase 3 SAPPHIRE clinical trial. SAPPHIRE, a randomized, double-blind, placebo-controlled clinical trial evaluating apitegromab for patients with non-ambulatory Types 2 and 3 SMA on either nusinersen or risdiplam, is actively enrolling SMA patients across 55 sites in the
U.S. andEurope . The anticipated enrollment is approximately 156 patients aged 2-12 in the main efficacy population.
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Presented new Phase 2 TOPAZ trial data indicating positive trends in quality-of-life measures over 24 months with apitegromab for nonambulatory patients with Types 2 and 3 SMA.
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SRK-181 is an investigational selective inhibitor of latent TGFβ1 activation and is being developed with the aim of overcoming resistance in patients with advanced cancer.
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Data from the Phase 1 DRAGON trial presented at the
Society for Immunotherapy of Cancer's Annual Meeting show that SRK-181 continues to be generally well tolerated with early indications of efficacy (as of the data cut-off date ofAugust 29 , 2022).- No dose-limiting toxicities were observed in patients participating in Part A, and all dose levels were generally well tolerated, including the recommended SRK-181 dose of 1500 mg q3w or 1000 mg q2w in combination with anti‑PD-(L)1 for Part B.
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In Part A2 of the trial (n=15), there was one confirmed partial response (“PR”) in a patient with anti-PD-1 resistant clear cell renal cell carcinoma at 800mg who remained in the study for 30 weeks. Response was assessed based on RECIST 1.1 by principal investigators. One ongoing patient in the 2400 mg dose group of Part A2 with head and neck cancer experienced a
29.4% tumor reduction. -
Enrollment in DRAGON Part B is ongoing. Across the cohorts, 14 patients have been dosed as of the data cut-off date. The recommended dose of 1500mg q3w or 1000mg q2w SRK-181 in combination with anti-PD-(L)1 was generally well tolerated. There was a confirmed PR in one ongoing patient with anti-PD-1 resistant clear cell renal cell carcinoma.
Scholar Rock will continue to provide updates at future scientific meetings.
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Data from the Phase 1 DRAGON trial presented at the
Corporate Updates
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Announced key leadership appointments:
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Jay Backstrom , M.D., M.P.H. was appointed President & CEO in October, bringing an exceptional range of research and development, regulatory, and leadership experience spanning several decades in the biopharmaceutical industry. He has been instrumental in organizing and executing development strategies and has led programs in a broad range of therapeutic areas through regulatory approvals.Dr. Backstrom most recently served as Executive Vice President, Research and Development at Acceleron Pharma, which was acquired by Merck in 2021. -
Jing L. Marantz , M.D., Ph.D., M.B.A., was appointed Chief Medical Officer in November.Dr. Marantz is an accomplished biopharmaceutical executive with over 20 years of industry experience spanning multiple specialties, including neurology, hematology/oncology, and rare diseases. Most recently, she served as the Executive Vice President and Chief Business Officer at Krystal Biotech. Previously, she was Senior Vice President and Head of Medical Affairs at Acceleron Pharma, where she also was a member of the R&D leadership team.
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Amended debt facility with
Oxford Finance andSilicon Valley Bank .Scholar Rock amended the existing debt facility withOxford Finance andSilicon Valley Bank . Under the agreement, an additional tranche is available at the company’s discretion and subject to meeting certain criteria. The amendment also extends both the interest-only period for an additional 24 months to$25 million November 2024 , and the loan maturity date toNovember 2027 .
Third Quarter 2022 Financial Results
For the quarter ended
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Revenue was
for the quarter ended$0 September 30, 2022 , compared to for the quarter ended$5.5 million September 30, 2021 .
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Research and development expense was
for the quarter ended$33.4 million September 30, 2022 , compared to for the quarter ended$31.3 million September 30, 2021 . The increase was primarily attributable to expenses related to non-cash equity-based compensation expense, a component of employee compensation and benefits costs.
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General and administrative expense was
for the quarter ended$10.5 million September 30, 2022 , compared to for the quarter ended$11.3 million September 30, 2021 . The decrease was attributable to the reduction of employee severance and benefits expenses that were recognized during the same period in the prior year.
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As of
September 30, 2022 ,Scholar Rock had cash, cash equivalents, and marketable securities of approximately , which is expected to fund the Company’s anticipated operating and capital expenditure requirements into 2025.$343.7 million
“With the successful equity financing that we completed in the second quarter and the added flexibility provided by the amendment of our debt facility, we are well funded to advance our pipeline through key milestones,” said
About
Availability of Other Information About Scholar Rock
Investors and others should note that we communicate with our investors and the public using our company website www.scholarrock.com, including, but not limited to, company disclosures, investor presentations and FAQs,
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Forward-Looking Statements
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding Scholar Rock’s future expectations, plans and prospects, including without limitation, Scholar Rock’s expectations regarding its growth, strategy, progress and timing of its clinical trials for apitegromab, SRK-181, and other product candidates and indication selection and development timing, its cash runway, the ability of any product candidate to perform in humans in a manner consistent with earlier nonclinical, preclinical or clinical trial data, and the potential of its product candidates and proprietary platform. The use of words such as “may,” “might,” “could,” “will,” “should,” “expect,” “plan,” “anticipate,” “believe,” “estimate,” “project,” “intend,” “future,” “potential,” or “continue,” and other similar expressions are intended to identify such forward-looking statements. All such forward-looking statements are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, without limitation, that preclinical and clinical data, including the results from the Phase 2 clinical trial of apitegromab, or Part A of the Phase 1 clinical trial of SRK-181, are not predictive of, may be inconsistent with, or more favorable than, data generated from future clinical trials of the same product candidate, including, without limitation, the Phase 3 clinical trial of apitegromab in SMA or Part B of the Phase 1 clinical trial of SRK-181, Scholar Rock’s ability to provide the financial support, resources and expertise necessary to identify and develop product candidates on the expected timeline, the data generated from Scholar Rock’s nonclinical and preclinical studies and clinical trials, information provided or decisions made by regulatory authorities, competition from third parties that are developing products for similar uses, Scholar Rock’s ability to obtain, maintain and protect its intellectual property, Scholar Rock’s dependence on third parties for development and manufacture of product candidates including, without limitation, to supply any clinical trials, Scholar Rock’s ability to manage expenses and to obtain additional funding when needed to support its business activities and establish and maintain strategic business alliances and new business initiatives, and the impacts of public health pandemics such as COVID-19 on business operations and expectations, as well as those risks more fully discussed in the section entitled "Risk Factors" in Scholar Rock’s Quarterly Report on Form 10-Q for the quarter ended
Condensed Consolidated Statements of Operations | ||||||||||||||||
(unaudited) | ||||||||||||||||
(in thousands, except share and per share data) | ||||||||||||||||
Three Months Ended |
Nine Months Ended |
|||||||||||||||
|
2022 |
|
|
2021 |
|
|
2022 |
|
|
2021 |
|
|||||
Revenue | $ |
— |
|
$ |
5,464 |
|
$ |
33,193 |
|
$ |
14,767 |
|
||||
Operating expenses | ||||||||||||||||
Research and development |
|
33,392 |
|
|
31,265 |
|
|
94,831 |
|
|
79,417 |
|
||||
General and administrative |
|
10,470 |
|
|
11,276 |
|
|
32,304 |
|
|
29,907 |
|
||||
Total operating expenses |
|
43,862 |
|
|
42,541 |
|
|
127,135 |
|
|
109,324 |
|
||||
Loss from operations |
|
(43,862 |
) |
|
(37,077 |
) |
|
(93,942 |
) |
|
(94,557 |
) |
||||
Other income (expense), net |
|
565 |
|
|
(430 |
) |
|
(1,305 |
) |
|
(1,328 |
) |
||||
Net loss | $ |
(43,297 |
) |
$ |
(37,507 |
) |
$ |
(95,247 |
) |
$ |
(95,885 |
) |
||||
Net loss per share, basic and diluted | $ |
(0.55 |
) |
$ |
(1.02 |
) |
$ |
(1.80 |
) |
$ |
(2.62 |
) |
||||
Weighted average common shares outstanding, basic and diluted |
|
79,336,161 |
|
|
36,683,026 |
|
|
52,958,447 |
|
|
36,549,833 |
|
Condensed Consolidated Balance Sheets | |||||||
(unaudited) | |||||||
(in thousands) | |||||||
Assets | |||||||
Cash, cash equivalents and marketable securities | $ |
343,655 |
$ |
252,994 |
|||
Other current assets |
|
13,957 |
|
12,325 |
|||
Total current assets |
|
357,612 |
|
265,319 |
|||
Other assets |
|
32,691 |
|
39,126 |
|||
Total assets | $ |
390,303 |
$ |
304,445 |
|||
Liabilities and Stockholders' Equity | |||||||
Current liabilities | $ |
33,736 |
$ |
64,297 |
|||
Long-term liabilities |
|
63,302 |
|
68,074 |
|||
Total liabilities |
|
97,038 |
|
132,371 |
|||
Total stockholders' equity |
|
293,265 |
|
172,074 |
|||
Total liabilities and stockholders' equity | $ |
390,303 |
$ |
304,445 |
|||
View source version on businesswire.com: https://www.businesswire.com/news/home/20221114005195/en/
Investors
Rushmie Nofsinger
rnofsinger@scholarrock.com
ir@scholarrock.com
857-259-5573
Media
ariane.lovell@finnpartners.com
media@scholarrock.com
917-565-2204
Source:
FAQ
What were Scholar Rock's financial results for Q3 2022?
What is the latest update on Scholar Rock's SAPPHIRE trial?
What is the significance of the TOPAZ trial data presented by Scholar Rock?
How has Scholar Rock's financial position changed?