Scholar Rock Reports Full Year 2021 Financial Results and Highlights Business Progress
Scholar Rock (SRRK) reported its financial results for 2021, highlighting a net loss of $131.8 million, or $3.59 per share, compared to a loss of $86.5 million the previous year. Revenue increased to $18.8 million, driven by a collaboration with Gilead. The company is focused on advancing its Phase 3 SAPPHIRE trial for apitegromab in spinal muscular atrophy, with results expected from the TOPAZ trial by mid-2022. Cash reserves stand at approximately $253 million, projected to sustain operations through mid-2023. Upcoming data from the DRAGON trial evaluating SRK-181 is also anticipated in 2022.
- Revenue increased to $18.8 million in 2021 from $15.4 million in 2020.
- Cash reserves of approximately $253 million expected to fund operations into mid-2023.
- Ongoing Phase 3 SAPPHIRE clinical trial for apitegromab shows strong patient retention.
- Expected data from the DRAGON trial may provide insights into oncological therapies.
- Net loss increased to $131.8 million in 2021 from $86.5 million in 2020.
- Research and development expenses rose to $108.5 million, impacting overall financial performance.
- Progressing Phase 3 SAPPHIRE clinical trial evaluating apitegromab in patients with non-ambulatory Type 2 and 3 Spinal Muscular Atrophy (SMA)
- Two-year data from open label extension of TOPAZ Phase 2 trial in SMA expected by mid-2022
- Data from DRAGON Part B proof-of-concept trial evaluating SRK-181 to overcome checkpoint inhibitor resistance in cancer patients anticipated in 2022
- Ended 2021 with approximately
“We are excited by the momentum and engagement around our ongoing Phase 3 SAPPHIRE trial of apitegromab in spinal muscular atrophy, as well as our DRAGON Phase 1 trial of SRK-181 in solid tumors. These programs have significant potential to address unmet patient need in a differentiated way, as well as demonstrate the tremendous potential of Scholar Rock’s platform, which focuses on inhibiting the activation of latent growth factors,” said
Company Updates and Upcoming Milestones
Apitegromab is a selective inhibitor of myostatin activation being developed as the potential first muscle-directed therapy for the treatment of spinal muscular atrophy (SMA).
- Conducting SAPPHIRE Phase 3 Clinical Trial Evaluating Apitegromab in Patients with Non-Ambulatory Type 2 and 3 SMA. The randomized, double-blind, placebo-controlled Phase 3 clinical trial is evaluating apitegromab as add-on therapy for patients on either nusinersen or risdiplam. The study design plans for approximately 156 patients aged 2-12 years old with non-ambulatory Type 2 and 3 SMA to be enrolled in the main efficacy population. Patients will be randomized 1:1:1 to receive for 12 months either apitegromab 20 mg/kg, apitegromab 10 mg/kg, or placebo by intravenous (IV) infusion every 4 weeks in addition to background SMN treatment.
-
Data from TOPAZ Phase 2 Open Label Extension Trial Expected to be Presented by mid-2022. As of
February 28, 2022 , 55 of 57 patients remain enrolled in the long-term extension trial of apitegromab in Type 2 and Type 3 SMA.
SRK-181 is a selective inhibitor of latent TGFβ1 activation being developed with the aim of overcoming primary resistance to and increasing the number of patients who may benefit from checkpoint inhibitor therapy.
-
Advancing Part B of the DRAGON Phase 1 POC Trial for SRK-181. Based on the safety and pharmacokinetic data from Part A of the DRAGON Phase 1 trial,
Scholar Rock is conducting the Part B dose expansion portion of the trial, in which SRK-181 is dosed at 1500 mg every three weeks (Q3W) in patients receiving an approved anti-PD-(L)1 therapy dosed Q3W, or 1000 mg every two weeks (Q2W) in patients receiving an approved anti-PD-(L)1 therapy dosed Q2W. Part B consists of multiple proof-of-concept cohorts focused upon evaluating the ability of SRK-181 to overcome primary resistance to anti-PD-(L)1 therapy. Each cohort will enroll up to 40 patients with various solid tumors, including urothelial carcinoma (UC), cutaneous melanoma (MEL), non-small cell lung cancer (NSCLC), clear cell renal cell carcinoma (ccRCC), and other solid tumors. The biomarker strategy in part B of DRAGON will explore early signs of SRK-181 activity, including target engagement and pathway modulation. This will include measuring effects on both circulating and tumor immune contexture, such as CD8+ T cell infiltration and reductions in myeloid-derived suppressor cell (MDSC) populations as well as analysis of TGFβ-related pathway signaling. Early efficacy and safety data are anticipated in 2022.
Full Year 2021 Financial Results
For the full year ended
-
Revenue was
for the year ended$18.8 million December 31, 2021 compared to for the year ended$15.4 million December 31, 2020 . Revenue was related to the Gilead fibrosis-focused research collaboration, which concluded inDecember 2021 . -
Research and development expense was
for the year ended$108.5 million December 31, 2021 compared to for the year ended$74.1 million December 31, 2020 . The increase year-over-year was primarily attributable to planned spend associated with apitegromab development, including costs associated with clinical drug supply manufacturing and costs associated with our SAPPHIRE trial, as well as higher personnel-related costs. -
General and administrative expense was
for the year ended$40.3 million December 31, 2021 compared to for the year ended$28.2 million December 31, 2020 . The increase year-over-year was primarily attributable to professional services and higher personnel-related costs, including filling key positions essential to progressing research, development and pre-commercial activities.
As of
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, 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 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 |
|
||||||
|
|
|
|
2021 |
|
|
|
2020 |
|
|
|
|
|
|
|
|
|
||||
|
Revenue |
$ |
18,816 |
|
|
$ |
15,403 |
|
|
|
|
|
|
|
|
|
|
||||
|
Operating expenses |
|
|
|
|
|||||
|
|
Research and development |
|
108,468 |
|
|
|
74,062 |
|
|
|
|
General and administrative |
|
40,269 |
|
|
|
28,219 |
|
|
|
Total operating expenses |
|
148,737 |
|
|
|
102,281 |
|
|
|
|
Loss from operations |
|
(129,921 |
) |
|
|
(86,878 |
) |
|
|
|
Other income (expense), net |
|
(1,878 |
) |
|
|
395 |
|
|
|
|
Net loss |
$ |
(131,799 |
) |
|
$ |
(86,483 |
) |
|
|
|
|
|
|
|
|
|
||||
|
Net loss per share, basic and diluted |
$ |
(3.59 |
) |
|
$ |
(2.81 |
) |
|
|
|
|
|
|
|
|
|
||||
|
Weighted average common shares outstanding, basic and diluted |
|
36,711,833 |
|
|
|
30,734,109 |
|
|
|
|
|
|
|
|
|
|
|
|
|||||
|
|
Condensed Consolidated Balance Sheets |
|||||
|
|
(unaudited) |
|||||
|
|
(in thousands) |
|||||
|
|
|
|
|
|
||
|
|
|
|
|
|
||
|
Assets |
|
|
|
|||
|
|
Cash, cash equivalents and marketable securities |
$ |
252,994 |
|
$ |
341,031 |
|
|
Other current assets |
|
12,325 |
|
|
3,373 |
|
|
Total current assets |
|
265,319 |
|
|
344,404 |
|
|
Other assets |
|
39,126 |
|
|
43,901 |
|
Total assets |
$ |
304,445 |
|
$ |
388,305 |
|
|
|
|
|
|
|
||
|
Liabilities and Stockholders' Equity |
|
|
|
|||
|
|
Current liabilities |
$ |
64,297 |
|
$ |
42,564 |
|
|
Long-term liabilities |
|
68,074 |
|
|
84,971 |
|
|
Total liabilities |
|
132,371 |
|
|
127,535 |
|
|
Total stockholders' equity |
|
172,074 |
|
|
260,770 |
|
Total liabilities and stockholders' equity |
$ |
304,445 |
|
$ |
388,305 |
View source version on businesswire.com: https://www.businesswire.com/news/home/20220307005079/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 is Scholar Rock's stock symbol?
What were Scholar Rock's financial results for 2021?
What are the upcoming milestones for Scholar Rock in 2022?
How much cash does Scholar Rock have as of December 31, 2021?