Omega Therapeutics, Inc. (Nasdaq: OMGA) ("Omega"), a clinical-stage biotechnology company pioneering the first systematic approach to use mRNA therapeutics as a new class of programmable epigenetic medicines by leveraging its OMEGA Epigenomic Programming™ platform, today announced financial results for the second quarter ended June 30, 2022, and highlighted recent Company progress.
"This has been an exciting second quarter for Omega, in which we were thrilled to receive FDA clearance of our first IND application for OTX-2002, representing the first ever Omega Epigenomic ControllerTM, a new class of programmable mRNA therapeutics. This is a critical milestone for Omega as we enter our next phase of growth and reflects our pioneering work to realize the potential of epigenomic programming," said Mahesh Karande, President and Chief Executive Officer of Omega Therapeutics. "Additionally, we were also pleased to share exciting, new supportive preclinical data, both from our lead program OTX-2002 in hepatocellular carcinoma, as well as from another program in our pipeline focused on non-small cell lung cancer, a potential future indication. We look forward to continuing this momentum as we enter the clinic in the second half of this year and further exploring the broad ranging capabilities of our novel platform in additional therapeutic areas."
Recent Business Highlights
Development Pipeline and Platform
Corporate
Second Quarter 2022 Financial Results
As of June 30, 2022, the Company had cash, cash equivalents and marketable securities totaling $173.7 million.
Research and development (R&D) expenses for the second quarter of 2022 were $19.4 million, compared to $11.2 million for the second quarter of 2021. The $8.2 million increase in R&D expense was primarily driven by an increase in personnel-related expenses, external manufacturing costs, and study costs in support of the advancement of our programs
General and administrative (G&A) expenses for the second quarter of 2022 were $6.2 million, compared to $3.6 million for the second quarter of 2021. The $2.6 million increase in G&A expense was primarily driven by an increase in personnel-related expenses to support business growth.
Net loss for the second quarter of 2022 was $25.9 million, compared to $15.4 million for the second quarter of 2021, driven predominantly by increased R&D and G&A expenses to support the Company's growth and operations as a public company.
About Omega Therapeutics
Omega Therapeutics, founded by Flagship Pioneering, is a clinical-stage biotechnology company pioneering the first systematic approach to use mRNA therapeutics as a new class of programmable epigenetic medicines. The company's OMEGA Epigenomic Programming™ platform harnesses the power of epigenetics, the mechanism that controls gene expression and every aspect of an organism's life from cell genesis, growth, and differentiation to cell death. Using a suite of technologies, paired with Omega's process of systematic, rational, and integrative drug design, the OMEGA platform enables control of fundamental epigenetic processes to correct the root cause of disease by returning aberrant gene expression to a normal range without altering native nucleic acid sequences. Omega's modular and programmable mRNA medicines, Omega Epigenomic Controllers™, are designed to target specific epigenomic loci within insulated genomic domains, EpiZips, from amongst thousands of unique, mapped, and validated genome-wide DNA-sequences, with high specificity to durably tune single or multiple genes to treat and cure diseases through Precision Genomic Control™. Omega is currently advancing a broad pipeline of development candidates spanning a range of disease areas, including oncology, regenerative medicine, multigenic diseases including immunology, and select monogenic diseases, including alopecia.
For more information, visit omegatherapeutics.com, or follow us on Twitter and LinkedIn.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including without limitation statements regarding the timing and design of our Phase 1/2 MYCHELANGELOTM clinical trial; the potential of the OMEGA platform to engineer programmable epigenetic mRNA therapeutics that successfully regulate gene expression by targeting insulated genomic domains; expectations surrounding the potential of our product candidates, including our lead OEC candidate OTX-2002; and expectations regarding our pipeline, including trial design, initiation of preclinical studies and advancement of multiple preclinical development programs in oncology, immunology, regenerative medicine, and select monogenic diseases. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the novel technology on which our product candidates are based makes it difficult to predict the time and cost of preclinical and clinical development and subsequently obtaining regulatory approval, if at all; the substantial development and regulatory risks associated with epigenomic controller machines due to the novel and unprecedented nature of this new category of medicines; our limited operating history; the incurrence of significant losses and the fact that we expect to continue to incur significant additional losses for the foreseeable future; our need for substantial additional financing; our investments in research and development efforts that further enhance the OMEGA platform, and their impact on our results; uncertainty regarding preclinical development, especially for a new class of medicines such as epigenomic controllers; potential delays in and unforeseen costs arising from our clinical trials; the fact that our product candidates may be associated with serious adverse events, undesirable side effects or have other properties that could halt their regulatory development, prevent their regulatory approval, limit their commercial potential, or result in significant negative consequences; the impact of increased demand for the manufacture of mRNA and LNP based vaccines to treat COVID-19 on our development plans; difficulties manufacturing the novel technology on which our OEC candidates are based; our ability to adapt to rapid and significant technological change; our reliance on third parties for the manufacture of materials; our ability to successfully acquire and establish our own manufacturing facilities and infrastructure; our reliance on a limited number of suppliers for lipid excipients used in our product candidates; our ability to advance our product candidates to clinical development; and our ability to obtain, maintain, enforce and adequately protect our intellectual property rights. These and other important factors discussed under the caption "Risk Factors" in our Quarterly Report on Form 10-Q for the quarter ended June 30, 2022, and our other filings with the SEC could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, we disclaim any obligation to do so, even if subsequent events cause our views to change.
Investor contact:
Kevin Murphy
Argot Partners
212.600.1902
This email address is being protected from spambots. You need JavaScript enabled to view it.
Media contact:
Jason Braco, Ph.D.
LifeSci Communications
646.751.4361
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Omega Therapeutics, Inc. | |||||||||||||||
Condensed consolidated statements of operations and comprehensive loss | |||||||||||||||
(thousands, except share and per share amounts) | |||||||||||||||
Three Months Ended June 30, | Six Months Ended June 30, | ||||||||||||||
2022 | 2021 | 2022 | 2021 | ||||||||||||
Collaboration revenue from related party | $ | 476 | $ | — | $ | 743 | $ | — | |||||||
Operating expenses: | |||||||||||||||
Research and development | 19,387 | 11,184 | 33,659 | 20,933 | |||||||||||
General and administrative | 6,202 | 3,637 | 11,336 | 6,452 | |||||||||||
Related party expense, net | 741 | 384 | 1,562 | 763 | |||||||||||
Total operating expenses | 26,330 | 15,205 | 46,557 | 28,148 | |||||||||||
Loss from operations | (25,854) | (15,205) | (45,814) | (28,148) | |||||||||||
Other expense, net: | |||||||||||||||
Interest expense, net | (55) | (190) | (210) | (402) | |||||||||||
Change in fair value of warrant liability | — | (11) | — | (340) | |||||||||||
Other expense, net | (3) | (4) | (52) | (8) | |||||||||||
Total other expense, net | (58) | (205) | (262) | (750) | |||||||||||
Net loss | $ | (25,912) | $ | (15,410) | $ | (46,076) | $ | (28,898) | |||||||
Net loss per common stock attributable to common stockholders, basic and diluted | $ | (0.54) | $ | (3.36) | $ | (0.96) | $ | (6.36) | |||||||
Weighted-average common stock used in net loss per share attributable to common stockholders, basic and diluted | 47,849,639 | 4,588,500 | 47,828,594 | 4,542,832 | |||||||||||
Comprehensive loss: | |||||||||||||||
Net loss | $ | (25,912) | $ | (15,410) | $ | (46,076) | $ | (28,898) | |||||||
Other comprehensive loss: | |||||||||||||||
Unrealized loss on marketable securities | (147) | — | (944) | — | |||||||||||
Comprehensive loss | $ | (26,059) | $ | (15,410) | $ | (47,020) | $ | (28,898) |
Omega Therapeutics, Inc. | ||||||||
Condensed Consolidated Balance Sheets | ||||||||
(thousands) | ||||||||
June 30, | December 31, | |||||||
2022 | 2021 | |||||||
Assets | ||||||||
Cash and cash equivalents | $ | 90,857 | $ | 186,482 | ||||
Marketable securities | 82,808 | 38,845 | ||||||
Other assets | 19,381 | 8,006 | ||||||
Total assets | $ | 193,046 | $ | 233,333 | ||||
Liabilities and stockholders' equity | ||||||||
Liabilities | $ | 35,662 | $ | 32,705 | ||||
Stockholders' equity | 157,384 | 200,628 | ||||||
Total liabilities and stockholders' equity | $ | 193,046 | $ | 233,333 | ||||
Last Trade: | US$0.83 |
Daily Change: | 0.02 2.59 |
Daily Volume: | 137,001 |
Market Cap: | US$46.070M |
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