Scholar Rock Reports Full Year 2022 Financial Results and Highlights Business Progress
Scholar Rock (NASDAQ: SRRK) reported its financial results for 2022, noting a net loss of $134.5 million or $2.26 per share, compared to a loss of $131.8 million or $3.59 per share in 2021. Revenue increased to $33.2 million from $18.8 million, mainly from a now-ended collaboration with Gilead. The company is on track to complete the pivotal Phase 3 SAPPHIRE trial for apitegromab in 2023, with data readout expected in 2024. Cash reserves stand at approximately $315 million, projected to fund operations into 2025. New Chief Commercial Officer, Tracey M. Sacco, has been appointed to lead commercial strategy.
- Revenue increased to $33.2 million in 2022 from $18.8 million in 2021.
- Completion of the pivotal Phase 3 SAPPHIRE trial for apitegromab is on track for 2023.
- Cash reserves of approximately $315 million expected to fund operations into 2025.
- Appointment of Tracey M. Sacco as Chief Commercial Officer to enhance commercial strategy.
- Net loss widened to $134.5 million in 2022 from $131.8 million in 2021.
- Increased research and development expenses to $124.4 million in 2022 due to clinical trial costs.
- Enrollment of pivotal Phase 3 SAPPHIRE trial evaluating apitegromab on track for completion in 2023, and 36-month extension data from Phase 2 TOPAZ trial expected in mid-2023
- Phase 1 DRAGON trial of SRK-181 continues to advance with biomarker and clinical data updates planned in 2023
- Company expanded commercial experience with recent appointment of Chief Commercial Officer
- Ended 2022 with approximately
“2023 is off to a great start as we continue to build upon our momentum from last year. Importantly, we are on track to complete the enrollment of our pivotal SAPPHIRE trial of apitegromab and are looking forward to providing 36-month extension data from the Phase 2 TOPAZ trial of apitegromab in the coming months. Additionally, we look forward to sharing biomarker and clinical updates throughout the year from the SRK-181 Phase 1 DRAGON trial in patients with relapsed and/or refractory cancers resistant to checkpoint inhibitor therapy,” said
Company Highlights and Upcoming Milestones
Apitegromab is a selective inhibitor of latent myostatin activation being developed as the potential first muscle-targeted therapy for the treatment of spinal muscular atrophy (SMA).
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Continue to progress and complete enrollment of Phase 3 SAPPHIRE clinical trial. The last patient is expected to be enrolled in SAPPHIRE in 2023, with the top-line data readout expected in 2024. If successful, and if approved, the company expects to initiate a commercial product launch in 2025. SAPPHIRE is a randomized, double-blind, placebo-controlled Phase 3 clinical trial evaluating apitegromab in patients with nonambulatory Types 2 and 3 SMA on either nusinersen or risdiplam. The
U.S. Food and Drug Administration (FDA) has granted Fast Track, Orphan Drug, and Rare Pediatric Disease designations, and theEuropean Medicines Agency (EMA) has granted Priority Medicines (PRIME) and Orphan designations to apitegromab for the treatment of SMA. -
36-month extension data from Phase 2 TOPAZ trial to be presented in mid-2023. As of
December 31, 2022 , approximately 90 percent of patients who entered the trial’s long-term extension study (51/57) remained on study. At theCure SMA Research & Clinical Care Meeting inJune 2022 , the company presented 24-month extension data from the TOPAZ trial which demonstrated sustained gains in Hammersmith Functional Motor Scale Expanded (HFMSE), increased Revised Upper Limb Module (RULM) scores, and positive trends in quality-of-life data for nonambulatory patients with Types 2 and 3 SMA receiving an SMN therapy.
SRK-181 is an investigational selective inhibitor of latent TGFβ-1 activation and is being developed with the aim of overcoming resistance to checkpoint therapy in patients with advanced cancer.
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Continue to progress Phase 1 DRAGON trial. The company expects to provide biomarker and clinical updates from the DRAGON proof-of-concept trial throughout 2023. In
November 2022 ,Scholar Rock presented data from DRAGON at theSociety for Immunotherapy of Cancer’s (SITC) Annual Meeting that showed SRK-181 continued to be generally well tolerated with early indications of efficacy (as of the data cut-off date ofAugust 29, 2022 ). -
Encore data from DRAGON will be presented at the
European Society for Medical Oncology Targeted Anticancer Therapies (ESMO TAT)Congress inParis, France onMarch 7 at11:05-12:30 p.m. EST . The presentation is titled “Safety and efficacy results of SRK-181 (a latent TGFβ1 inhibitor) from a phase 1 trial (DRAGON trial).”
Corporate
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Appointed
Tracey M. Sacco as Chief Commercial Officer. InFebruary 2023 ,Ms. Sacco joinedScholar Rock to build and lead all commercial functions, including sales, marketing, market access, and commercial operations. She will help the company prepare for the potential commercial launch of apitegromab, if approved.Ms. Sacco brings extensive biopharmaceutical industry experience, including commercial strategy and global launch experience of rare disease products.
Full Year 2022 Financial Results
For the full year ended
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Revenue was
for the year ended$33.2 million December 31, 2022 , compared to for the year ended$18.8 million December 31, 2021 . Revenue recognized during both periods was associated with the Gilead collaboration which ended in 2022.
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Research and development expense was
for the year ended$124.4 million December 31, 2022 , compared to for the year ended$108.5 million December 31, 2021 . The increase was primarily attributable to costs associated with running the company’s Phase 3 SAPPHIRE pivotal trial for apitegromab in SMA, including clinical trials costs as well as costs associated with employee compensation and benefits.
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General and administrative expense was
for the year ended$43.1 million December 31, 2022 , compared to for the year ended$40.3 million December 31, 2021 . The increase was due to an increase in employee compensation and benefits, primarily associated with equity-based compensation and professional fees.
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As of
December 31, 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.$315 million
“As Scholar Rock works to develop transformative therapies for patients with our highly differentiated platform, we are entering 2023 with an experienced team, a strong balance sheet, and a clear line of sight to important anticipated milestones, all of which are expected to help advance the next phase of growth for the company,” said
About
Scholar Rock® is a registered trademark of
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, and are not predictive of, may be inconsistent with, or more favorable than, data generated from future clinical trials of the same product candidates, 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 Annual Report on Form 10-K for the year ended
Condensed Consolidated Statements of Operations | |||||||||
(unaudited) | |||||||||
(in thousands, except share and per share data) | |||||||||
Years Ended |
|||||||||
|
2022 |
|
|
2021 |
|
||||
Revenue | $ |
33,193 |
|
$ |
18,816 |
|
|||
Operating expenses | |||||||||
Research and development |
|
124,444 |
|
|
108,468 |
|
|||
General and administrative |
|
43,119 |
|
|
40,269 |
|
|||
Total operating expenses |
|
167,563 |
|
|
148,737 |
|
|||
Loss from operations |
|
(134,370 |
) |
|
(129,921 |
) |
|||
Other income (expense), net |
|
(132 |
) |
|
(1,878 |
) |
|||
Net loss | $ |
(134,502 |
) |
$ |
(131,799 |
) |
|||
Net loss per share, basic and diluted | $ |
(2.26 |
) |
$ |
(3.59 |
) |
|||
Weighted average common shares outstanding, basic and diluted |
|
59,611,656 |
|
|
36,711,833 |
|
Condensed Consolidated Balance Sheets | ||||||
(unaudited) | ||||||
(in thousands) | ||||||
Assets | ||||||
Cash, cash equivalents and marketable securities | $ |
315,361 |
$ |
252,994 |
||
Other current assets |
|
12,663 |
|
12,325 |
||
Total current assets |
|
328,024 |
|
265,319 |
||
Other assets |
|
30,144 |
|
39,126 |
||
Total assets | $ |
358,168 |
$ |
304,445 |
||
Liabilities and Stockholders' Equity | ||||||
Current liabilities | $ |
36,389 |
$ |
64,297 |
||
Long-term liabilities |
|
61,544 |
|
68,074 |
||
Total liabilities |
|
97,933 |
|
132,371 |
||
Total stockholders' equity |
|
260,235 |
|
172,074 |
||
Total liabilities and stockholders' equity | $ |
358,168 |
$ |
304,445 |
View source version on businesswire.com: https://www.businesswire.com/news/home/20230307005330/en/
Investors
Rushmie Nofsinger
rnofsinger@scholarrock.com
ir@scholarrock.com
857-259-5573
Media
ariane.lovell@finnpartners.com
media@scholarrock.com
917-565-2204
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