Press release

Geron to Announce Fourth Quarter and Full-Year 2023 Financial Results on February 28, 2024

FOSTER CITY, Calif.--(BUSINESS WIRE)-- Geron Corporation (Nasdaq: GERN), a late-stage clinical biopharmaceutical company, today announced that it will

articleGeron CorporationFebruary 14, 20243/company/geron-corporation/news/geron-to-announce-fourth-quarter-and-full-year-2023-financial-results-on-february-28
Geron to Announce Fourth Quarter and Full-Year 2023 Financial Results on February 28, 2024

About this update from Geron Corporation

[{"type":"text","content":" FOSTER CITY, Calif.--(BUSINESS WIRE)--\nGeron Corporation (Nasdaq: GERN), a late-stage clinical biopharmaceutical company, today announced that it will release its fourth quarter and full-year 2023 financial results and business highlights before the market opens on Wednesday, February 28, 2024 via press release, which will be available on the Company’s website at www.geron.com/investors. Geron will host a conference call to discuss the financial results as well as business highlights at 8:00 a.m. ET the same day.\n\n\nA live webcast of the conference call and related presentation will be available on the Company’s website at www.geron.com/investors/events. An archive of the webcast will be available on the Company’s website for 30 days.\n\n\nParticipants may access the webcast by registering online using the following link, https://events.q4inc.com/attendee/964382933\n\n\nAbout Geron\n\n\nGeron is a late-stage clinical biopharmaceutical company pursuing therapies with the potential to extend and enrich the lives of patients living with hematologic malignancies. Our first-in-class investigational telomerase inhibitor, imetelstat, harnesses Nobel Prize-winning science in a treatment that may alter the underlying drivers of disease. The New Drug Application (NDA) for imetelstat for the treatment of transfusion dependent anemia in patients with lower-risk myelodysplastic syndromes (LR-MDS) who have failed to respond or have lost response to or are ineligible for erythropoiesis-stimulating agents (ESAs), based on the results from the Phase 3 IMerge clinical trial, is currently under review by the United States Food and Drug Administration (FDA) with a Prescription Drug User Fee Act (PDUFA) target action date of June 16, 2024. In addition, an MAA is under review in the European Union for the same proposed indication. Furthermore, Geron currently has an ongoing pivotal Phase 3 clinical trial evaluating imetelstat in relapsed/refractory myelofibrosis (R/R MF). To learn more, visit www.geron.com or follow us on LinkedIn.\n\nView source version on businesswire.com: https://www.businesswire.com/news/home/20240214669884/en/\n\nAron Feingold\nVice President, Investor Relations and Corporate Communications\n\n\nKristen Kelleher\nSenior Manager, Investor Relations\n\n\[email protected]\[email protected]\n\n\nSource: Geron Corporation","leng...

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