Press Releases April 22, 2026 07:00 AM

Geron Plans to Announce First Quarter 2026 Financial Results on May 6, 2026

Geron Corporation schedules Q1 2026 financial results release and webcast for May 6, 2026

By Maya Rios
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Geron Corporation, a commercial-stage biopharmaceutical company focused on blood cancer treatments, announced it will release its Q1 2026 financial results and business highlights on May 6, 2026. The company will host a conference call and webcast to discuss these results. Geron is currently advancing its first-in-class telomerase inhibitor RYTELO® (imetelstat), approved for certain patients with lower-risk myelodysplastic syndromes and running pivotal Phase 3 trials in myelofibrosis and other hematologic malignancies.

Geron Plans to Announce First Quarter 2026 Financial Results on May 6, 2026
GERN
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Key Points

  • Geron to release Q1 2026 financial results and business update on May 6, 2026.
  • RYTELO® (imetelstat) is approved in the US and EU for treatment of specific lower-risk myelodysplastic syndromes.
  • Ongoing pivotal Phase 3 clinical trial for imetelstat in JAK-inhibitor relapsed or refractory myelofibrosis and other hematologic cancer studies.

FOSTER CITY, Calif., April 22, 2026 (GLOBE NEWSWIRE) -- Geron Corporation (Nasdaq: GERN), a commercial-stage biopharmaceutical company aiming to change lives by changing the course of blood cancer, today announced that it will release its first quarter 2026 financial results and business highlights before the market opens on Wednesday, May 6, 2026 via press release, which will be available on the Investors and Media section of the Company’s website. Geron will host a conference call and webcast at 8:00 a.m. Eastern Time.

A live and archived audio webcast of the conference call will be available from the Investors and Media section of the Company’s website at www.geron.com.

About Geron
Geron is a commercial-stage biopharmaceutical company aiming to change lives by changing the course of blood cancer. Our first-in-class telomerase inhibitor RYTELO® (imetelstat) is approved in the United States and the European Union for the treatment of certain adult patients with lower-risk myelodysplastic syndromes with transfusion dependent anemia. We are also conducting a pivotal Phase 3 clinical trial of imetelstat in JAK-inhibitor relapsed/refractory myelofibrosis, as well as studies in other hematologic malignancies. Inhibiting telomerase activity, which is increased in malignant stem and progenitor cells in the bone marrow, aims to potentially reduce proliferation and induce death of malignant cells. To learn more, visit www.geron.com or follow us on LinkedIn.

Investors and Media
Dawn Schottlandt
Senior Vice President, Investor Relations and Corporate Affairs
[email protected]


Risks

  • Clinical trial outcomes, especially the pivotal Phase 3 trial results, could impact future prospects.
  • Market acceptance and commercial uptake of RYTELO® could affect revenue growth.
  • Regulatory risks relating to further approvals and ongoing compliance in US and EU markets.

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