Communiqués Celcuity Inc.

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CELC

US15102K1007

Recherche biotechnologique et médicale

Marché Fermé - Nasdaq 22:00:00 04/09/2026			Varia. 5j.	Varia. 1 janv.
95,70 ^USD	-0,76%		+8,21%	-4,05%

26/08	Celcuity Inc dépose une demande d'autorisation de mise sur le marché complémentaire auprès de la FDA pour Revtorpyk (gedatolisib) dans le traitement du cancer du sein localement avancé ou métastatique HR+/HER2- avec mutation PIK3CA	CI
26/08	Celcuity dépose une demande d'homologation complémentaire pour le REVTORPYK dans le traitement du cancer du sein présentant une mutation PIK3CA	MT

Communiqués

01/09	Celcuity To Participate in Upcoming Investor Conferences	AQ
26/08	Celcuity Submits sNDA to FDA for REVTORPYK™ (gedatolisib) for HR+/HER2-, PIK3CA Mutant Locally Advanced or Metastatic Breast Cancer	AQ
13/08	Celcuity Inc. Reports Release of Second Quarter 2026 Financial Results and Provides Corporate Update	AQ
06/08	Celcuity Schedules Release of Second Quarter 2026 Financial Results and Webcast/Conference Call	AQ
30/07	Newly FDA-Approved REVTORPYK™ (gedatolisib) Included in the National Comprehensive Cancer Network® (NCCN®) Clinical Practice Guidelines for HR+/HER2- Locally Advanced or Metastatic Breast Cancer	AQ
14/07	Celcuity Announces FDA Approval of REVTORPYK™ (gedatolisib) for the Treatment of HR+/HER2-, PIK3CA Wild-Type Locally Advanced or Metastatic Breast Cancer	AQ
04/06	Celcuity Inc. Announces Pricing of Upsized Public Offering of 0.250% Convertible Senior Notes Due 2032	AQ
03/06	Celcuity Inc. Announces Public Offering of Convertible Senior Notes Due 2032	AQ
02/06	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	AQ
01/06	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	AQ
28/05	Celcuity To Participate in Upcoming Investor Conferences	AQ
14/05	Celcuity Inc. Reports Release of First Quarter 2026 Financial Results and Provides Corporate Update	AQ
14/05	Celcuity’s Phase 3 VIKTORIA-2 Trial of Gedatolisib as a First-Line Treatment for HR+/HER2- Advanced Breast Cancer Expanding to Include Endocrine-Sensitive Patients	AQ
07/05	Celcuity Schedules Release of First Quarter 2026 Financial Results and Webcast/Conference Call	AQ
01/05	Celcuity's Phase 3 VIKTORIA-1 Trial Achieves Primary Endpoint With Clinically Meaningful Improvement in Progression-Free Survival in PIK3CA Mutant Cohort	AQ
25/03	Celcuity Inc. Reports Release of Fourth Quarter and Full Year 2025 Financial Results and Provides Corporate Update	AQ
18/03	Celcuity Schedules Release of Fourth Quarter and Full Year 2025 Financial Results and Webcast/Conference Call	AQ
10/03	Celcuity : VIKTORIA-1 Trial of Gedatolisib Plus Fulvestrant With or Without Palbociclib in Hormone Receptor-Positive/HER2-/PIK3CA Wild-Type Advanced Breast Cancer	PU
09/03	Celcuity Announces Publication of Results from PIK3CA Wild-Type Cohort of Phase 3 VIKTORIA-1 Study of Gedatolisib Regimens in HR+/HER2- Advanced Breast Cancer in Journal of Clinical Oncology	AQ
25/02	Celcuity To Participate in Upcoming Investor Conferences	AQ
12/02	Celcuity Appoints Charles Romp to its Board of Directors	AQ
04/02	Celcuity to Present at Upcoming Guggenheim Emerging Outlook: Biotech Summit 2026	AQ
20/01	Celcuity Announces FDA Acceptance of New Drug Application for Gedatolisib in HR+/HER2-/PIK3CA Wild-Type Advanced Breast Cancer	AQ
11/12	Celcuity Presents Updated Results from the PIK3CA Wild-Type Cohort of the Phase 3 VIKTORIA-1 Trial at the 2025 San Antonio Breast Cancer Symposium	AQ
11/12	Gedatolisib, a multitarget PI3K/AKT/mTOR inhibitor, plus fulvestrant with or without palbociclib for second-line treatment of patients with HR+/HER2-/ PIK3CA-WT advanced breast cancer: updated results from the randomized, phase 3 VIKTORIA-1 trial	PU