Omega Therapeutics reported a net loss of $25.8 million for the third quarter of 2022, driven by increased R&D and G&A expenses. The company's cash, cash equivalents, and marketable securities totaled $148.3 million as of September 30, 2022. Key highlights included the first patient dosed in the Phase 1/2 MYCHELANGELO I trial of OTX-2002 and the selection of OTX-2101 for MYC-Driven Non-Small Cell Lung Cancer as a second development candidate.
First patient dosed in Phase 1/2 MYCHELANGELO I Trial of OTX-2002.
OTX-2002 granted Orphan Drug Designation by U.S. FDA for the treatment of Hepatocellular Carcinoma.
OTX-2101 for MYC-Driven Non-Small Cell Lung Cancer selected as second Omega Epigenomic Controller™ Development Candidate.
Company had $148.3 million in cash, cash equivalents and marketable securities as of September 30, 2022.
This press release contains forward-looking statements regarding the timing and design of clinical trials, the potential of the OMEGA platform, expectations surrounding product candidates, and expectations regarding the pipeline.
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