# Celcuity To Participate in Upcoming Investor Conferences
Canonical URL: https://biopharmsignal.com/news/CELC/celcuity-to-participate-in-upcoming-investor-conferences-b840e74b
Ticker: CELC
Company: Celcuity
Source: Celcuity
Published: 2026-05-28 12:30 EST
## Summary

Celcuity Inc. (Nasdaq: CELC), a clinical-stage biotechnology company focused on the development of targeted...

## Article Body
Celcuity Inc. (Nasdaq: CELC), a clinical-stage biotechnology company focused on the development of targeted therapies for the treatment of multiple solid tumor indications, today announced that Brian Sullivan, Chief Executive Officer and Co-founder of Celcuity, will present and be available for one-on-one investor meetings at the following investor conferences:

A fireside chat at the Jefferies Global Healthcare Conference at 1:25 p.m. EDT on Thursday, June 4, 2026. A live webcast will be available using this weblink: https://event.summitcast.com/view/NgCqua4VVQjq9ibVWHVWca/CMgAqyC4qKWHVGdLtG2QB8

A fireside chat at the Goldman Sachs 47th Annual Global Healthcare Conference 2026 at 8:00 a.m. EDT on Wednesday, June 10, 2026. A live webcast will be available using this weblink: https://event.webcasts.com/viewer/event.jsp?ei=1765258&tp_key=8bf99aba87

Alternatively, the live webcasts will be accessible from the Investors section of the company's website at https://ir.celcuity.com/events-presentations/ with a replay available shortly after the live events.

About Celcuity

Celcuity is a clinical-stage biotechnology company focused on the development of targeted therapies for the treatment of multiple solid tumor indications. Our lead therapeutic candidate is gedatolisib, a kinase inhibitor of the PI3K/AKT/mTOR (“PAM”) pathway that binds to all class I PI3K isoforms and the mTOR complexes, mTORC1 and mTORC2. By targeting all class I PI3K isoforms and mTORC1/2, gedatolisib induces comprehensive inhibition of the 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. Our Phase 3 clinical trial, VIKTORIA-1, evaluating gedatolisib in combination with fulvestrant with or without palbociclib in patients with hormone receptor positive (HR+), human epidermal growth factor receptor 2 negative (HER2-) (“HR+/HER2-”) locally advanced or metastatic breast cancer (“ABC”), has reported detailed results for Study 1, which evaluated patients with PIK3CA wild-type (“WT”) tumors, and announced topline results for Study 2, which evaluated patients with PIK3CA mutant-type (“MT”) tumors. Our Phase 3 clinical trial, VIKTORIA-2, is ongoing and incorporates two independent studies, Study 1 and Study 2, evaluating two separate cohorts of patients with ABC who are treatment-naive in the advanced setting. Study 1 is evaluating gedatolisib combined with palbociclib and fulvestrant as first-line treatment for patients with endocrine-resistant HR+/HER2- ABC. Study 2 is evaluating gedatolisib combined with palbociclib and letrozole as first-line treatment for patients with endocrine-sensitive HR+/HER2- ABC. A Phase 1b/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 at ClinicalTrials.gov . Celcuity is headquartered in Minneapolis, Minnesota. Further information about Celcuity can be found at www.celcuity.com . Follow us on LinkedIn and X .

Contacts:

Celcuity Inc. Brian Sullivan, bsullivan@celcuity.com Vicky Hahne, vhahne@celcuity.com (763) 392-0123 Jodi Sievers, jsievers@celcuity.com (415) 494-9924
## Recent Company News
- 2026-07-14 20:53 EST — [Celcuity Announces FDA Approval of REVTORPYK™ (gedatolisib) for the Treatment of HR+/HER2-, PIK3CA Wild-Type Locally Advanced or Metastatic Breast Cancer](https://biopharmsignal.com/news/CELC/celcuity-announces-fda-approval-of-revtorpyk-gedatolisib-for-the-treatment-of-hr-371190ee) — Source: Celcuity
- 2026-06-04 02:13 EST — [Celcuity Inc. Announces Pricing of Upsized Public Offering of 0.250% Convertible Senior Notes Due 2032](https://biopharmsignal.com/news/CELC/celcuity-inc-announces-pricing-of-upsized-public-offering-of-0-250-convertible-s-34cde08e) — Source: Celcuity
- 2026-06-03 11:19 EST — [Celcuity Inc. Announces Public Offering of Convertible Senior Notes Due 2032](https://biopharmsignal.com/news/CELC/celcuity-inc-announces-public-offering-of-convertible-senior-notes-due-2032-1a75ce4c) — Source: Celcuity
- 2026-06-02 12:25 EST — [Celcuity’s Gedatolisib Combination Regimens Doubled the Likelihood of Survival without Disease Progression or Death Compared to Alpelisib plus Fulvestrant in the PIK3CA Mutant Cohort of the Pivotal Phase 3 VIKTORIA-1 Trial in Patients with HR+/HER2- Advanced Breast Cancer](https://biopharmsignal.com/news/CELC/celcuity-s-gedatolisib-combination-regimens-doubled-the-likelihood-of-survival-w-bafa8e71) — Source: Celcuity
- 2026-06-01 12:30 EST — [Celcuity to Hold Conference Call to Discuss Results for the PIK3CA Mutant Cohort of the Phase 3 VIKTORIA-1 Clinical Trial of Gedatolisib Regimens in HR+/HER- Advanced Breast Cancer on June 2, 2026](https://biopharmsignal.com/news/CELC/celcuity-to-hold-conference-call-to-discuss-results-for-the-pik3ca-mutant-cohort-9ce6c49d) — Source: Celcuity
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