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Celcuity Schedules Release of First Quarter 2026 Financial Results and Webcast/Conference Call

Key Takeaway: Celcuity Inc. will release its financial results for Q1 2026 on May 14, 2026, after market close. A webcast and teleconference will follow at 4:30 p.m. ET to discuss the results and provide a corporate update. The company is focused on developing targeted therapies for oncology, with ongoing clinical trials for its lead candidate, gedatolisib.

Market Sentiment Analysis

POSITIVE FACTORS

  • Celcuity is advancing its clinical-stage therapies for oncology.
  • The upcoming financial results and corporate update indicate transparency and engagement.
  • Ongoing clinical trials show promise for their lead candidate, gedatolisib.

Full Press Release Details

MINNEAPOLIS, May 07, 2026 (GLOBE NEWSWIRE) -- Celcuity Inc. (Nasdaq: CELC), a clinical-stage biotechnology company pursuing development of targeted therapies for oncology, today announced that it will release its financial results for the first quarter 2026 after the market closes on Thursday, May 14, 2026. Management will host a webcast/teleconference the same day at 4:30 p.m. Eastern Time to discuss the results and provide a corporate update.

Webcast and Conference Call Information

To participate in the teleconference, domestic callers should dial 1-800-717-1738 and international callers should dial 1-646-307-1865. A live webcast presentation can also be accessed using this weblink:https://viavid.webcasts.com/starthere.jsp?ei=1760785&tp_key=2f73ec65ba. A replay of the webcast will be available on the Celcuity website following the live event.

About Celcuity

Celcuity is a clinical-stage biotechnology company pursuing the development of targeted therapies for the treatment of multiple solid tumor indications. The company's lead therapeutic candidate is gedatolisib, a potent, pan-PI3K and mTORC1/2 inhibitor that comprehensively blockades the PI3K/AKT/mTOR (“PAM”) pathway. Its mechanism of action and pharmacokinetic properties are differentiated from other currently approved and investigational therapies that target PI3Kα, AKT, or mTORC1 alone or together. A Phase 3 clinical trial, VIKTORIA-1, evaluating gedatolisib in combination with fulvestrant, with or without palbociclib, in patients with HR+/HER2- advanced breast cancer (“ABC”), has reported detailed results for thePIK3CAwild-type cohort and topline results for thePIK3CAmutant cohort. A Phase 3 clinical trial, VIKTORIA-2, evaluating gedatolisib in combination with a CDK4/6 inhibitor and fulvestrant as first-line treatment for patients with endocrine resistant HR+/HER2- ABC, is ongoing. A Phase 1/2 clinical trial, CELC-G-201, evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is ongoing. More detailed information about Celcuity’s active clinical trials can be found atClinicalTrials.gov. Celcuity is headquartered in Minneapolis. Further information about Celcuity can be found atwww.celcuity.com. Follow us onLinkedInandX.

Contacts:

Celcuity Inc.Brian Sullivan,bsullivan@celcuity.comVicky Hahne,vhahne@celcuity.com(763) 392-0123Jodi Sievers,jsievers@celcuity.com(415) 494-9924

Frequently Asked Questions

When will Celcuity release its Q1 2026 financial results?

Celcuity will release its Q1 2026 financial results on May 14, 2026.

What time is the Celcuity webcast for financial results?

The webcast will take place at 4:30 p.m. Eastern Time on May 14, 2026.

What is gedatolisib?

Gedatolisib is Celcuity's lead therapeutic candidate targeting multiple solid tumors.

What ongoing trials is Celcuity conducting?

Celcuity is conducting Phase 3 trials VIKTORIA-1 and VIKTORIA-2, and Phase 1/2 trial CELC-G-201.

Last updated: May 7, 2026