Welcome to our dedicated page for Erasca news (Ticker: ERAS), a resource for investors and traders seeking the latest updates and insights on Erasca stock.
Erasca Inc (NASDAQ: ERAS) operates in the clinical-stage biotechnology sector, where news flow is driven primarily by scientific and regulatory developments. This news page tracks announcements related to the company's RAS-targeting oncology programs, including clinical trial updates, regulatory filings, and corporate developments.
For a clinical-stage biotech focused on cancer drug development, material news typically includes data readouts from ongoing studies, regulatory interactions with the FDA, and updates on the advancement of drug candidates through clinical development phases. Erasca's focus on RAS-targeted therapies places it within a competitive area of oncology research, making pipeline progress announcements particularly significant.
The company regularly presents at oncology conferences such as the American Association for Cancer Research (AACR) Annual Meeting, where preclinical and clinical data are shared with the scientific community. These presentations often precede or accompany press releases detailing study results. Additionally, patent announcements provide insight into the company's intellectual property position and protection of its drug development programs.
Quarterly financial results provide visibility into Erasca's cash position and operational runway, critical metrics for evaluating clinical-stage biotechnology companies that do not yet generate product revenue. These reports detail research spending, progress toward clinical milestones, and management commentary on program prioritization.
Bookmark this page to follow Erasca's progress as it advances its oncology drug candidates through development.
Erasca, Inc. (Nasdaq: ERAS) announces key leadership changes with Lisa Tesvich-Bonora appointed as Chief People Officer and Robert Shoemaker promoted to Senior Vice President of Research. Tesvich-Bonora, with over 20 years of experience in organizational development, will lead initiatives in recruitment and professional development. Shoemaker, one of the company’s founding members, will integrate Discovery Research activities to enhance the development of Erasca’s oncology pipeline. These appointments aim to strengthen Erasca's culture and research capabilities.
Erasca, Inc. (Nasdaq: ERAS), a clinical-stage precision oncology company, will participate in the 40th annual J.P. Morgan Healthcare Conference on January 10, 2022, at 3:45 PM ET. During the event, CEO Jonathan E. Lim will present an overview of the company and its pipeline. Additionally, Dr. Lim and CFO David M. Chacko will engage in one-on-one investor meetings. A live audio webcast of the presentation will be accessible online, with an archived replay available for 30 days afterward.
Erasca has achieved FDA clearance for its investigational new drug (IND) application for ERAS-801, an EGFR inhibitor, ahead of schedule. This drug is designed for high CNS penetration to treat recurrent glioblastoma multiforme (rGBM) and will enter the THUNDERBBOLT-1 Phase 1 clinical trial in Q1 2022. The collaboration with the Global Coalition for Adaptive Research (GCAR) aims to explore a path for ERAS-801 within the GBM AGILE trial, enhancing the potential for expedited therapy development. With about 125,000 annual rGBM cases worldwide, this advancement addresses a significant unmet need.
Erasca, Inc. (Nasdaq: ERAS) has been added to the NASDAQ Biotech Index, effective December 20, 2021. This index tracks biotech and pharmaceutical companies listed on the Nasdaq, and membership requires meeting specific criteria, including market capitalization and trading volume. Erasca focuses on developing therapies for RAS/MAPK pathway-driven cancers and is backed by experts in precision oncology. This inclusion indicates recognition of the company's growth and stability in the biotechnology sector.
Erasca, Inc. (Nasdaq: ERAS), a precision oncology company focused on RAS/MAPK pathway-driven cancers, will participate in the Evercore ISI 4th Annual HealthCONx Conference on December 2, 2021. Jonathan E. Lim, M.D., CEO, and David M. Chacko, M.D., CFO, will engage in a "Fireside Chat" at 3:05 PM ET. Investors can register for the live webcast at Evercore.webcasts, with an archived replay available for 30 days on Erasca.com/events.
Erasca aims to develop innovative therapies targeting cancer pathways, leveraging expertise from top pioneers in the field.
Erasca, Inc. (Nasdaq: ERAS) reported strong execution in its recent financial results for Q3 2021, highlighting the initiation of two clinical trials for ERAS-007 in lung and gastrointestinal cancers. The company maintained a robust cash position of $487 million, bolstered by a $345 million IPO. Notably, it was named one of Fierce Biotech's "Fierce 15" innovative companies. However, the firm reported a net loss of $46.1 million for the quarter, influenced by significant R&D and G&A expenses, including a $17.5 million donation to the Erasca Foundation.
Erasca, Inc. (Nasdaq: ERAS) presented promising preclinical data for ERAS-801, a new EGFR inhibitor with significantly enhanced CNS penetration, at the AACR Conference. ERAS-801 shows a CNS penetration rate four times higher than existing EGFR inhibitors, demonstrating potent efficacy in over 90% of tested EGFR-mutant glioblastoma models. The company plans to submit an IND for refractory glioblastoma in Q1 2022. These advancements highlight ERAS-801's potential to improve outcomes for patients suffering from this aggressive cancer type.
Erasca, Inc. (Nasdaq: ERAS) announced the dosing of the first patient in the HERKULES-3 trial, a Phase 1b/2 clinical study evaluating ERAS-007, an ERK1/2 inhibitor, in combination with various agents for treating colorectal cancer (CRC). The trial aims to address mutations in BRAF, KRAS, and NRAS, impacting over half of CRC patients. Current therapies show limited effectiveness, with many patients experiencing rapid disease progression. HERKULES-3 will explore the safety and effectiveness of these combinations, potentially leading to significant advancements in CRC treatment.
ERAS-007, a leading ERK1/2 inhibitor, has entered Phase 1b/2 HERKULES-2 trial, focusing on advanced non-small cell lung cancer (NSCLC). Erasca, Inc. has initiated patient dosing to evaluate ERAS-007's effectiveness in combination with osimertinib. This trial aims to address unmet needs, especially for patients resistant to current therapies. The broad applicability of ERAS-007 was reinforced by recent preclinical findings showing strong anti-tumor activity, particularly in tumors with specific mutations. Future expansions will explore additional combinations across various cancer types.
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