Celcuity Announces Issuance of New Patent for Gedatolisib that Extends Patent Exclusivity into 2042
Celcuity (Nasdaq: CELC) has secured a new U.S. patent (No. 12,350,276) for the clinical dosing regimen of gedatolisib, its lead drug candidate for ER+/HER2- breast cancer patients. This patent extends the company's exclusivity until 2042.
The company's gedatolisib patent portfolio now includes 13 U.S. patents and 290 foreign patents, covering composition, formulations, and methods of use. Celcuity expects to release topline data from the VIKTORIA-1 clinical trial for the PIK3CA wild-type cohort in Q3 2025 and the PIK3CA mutant cohort in Q4 2025.
Celcuity (Nasdaq: CELC) ha ottenuto un nuovo brevetto statunitense (n. 12.350.276) relativo al regime di dosaggio clinico di gedatolisib, il suo principale candidato farmaco per pazienti con tumore al seno ER+/HER2-. Questo brevetto estende l'esclusività dell'azienda fino al 2042.
Il portafoglio brevetti di gedatolisib dell'azienda comprende ora 13 brevetti statunitensi e 290 brevetti esteri, che coprono composizione, formulazioni e metodi di utilizzo. Celcuity prevede di pubblicare i dati principali dello studio clinico VIKTORIA-1 per la coorte wild-type PIK3CA nel terzo trimestre 2025 e per la coorte mutante PIK3CA nel quarto trimestre 2025.
Celcuity (Nasdaq: CELC) ha obtenido una nueva patente en EE. UU. (No. 12,350,276) para el régimen de dosificación clínica de gedatolisib, su principal candidato a medicamento para pacientes con cáncer de mama ER+/HER2-. Esta patente extiende la exclusividad de la empresa hasta 2042.
La cartera de patentes de gedatolisib de la empresa ahora incluye 13 patentes estadounidenses y 290 patentes extranjeras, que cubren composición, formulaciones y métodos de uso. Celcuity espera publicar los datos principales del ensayo clínico VIKTORIA-1 para la cohorte PIK3CA tipo salvaje en el tercer trimestre de 2025 y para la cohorte mutante PIK3CA en el cuarto trimestre de 2025.
Celcuity (나스�: CELC)� ER+/HER2- 유방� 환자� 위한 주력 약물 후보� gedatolisib� 임상 투여 요법� 대� 새로� 미국 특허(번호 12,350,276)� 획득했습니다. � 특허� 회사� 독점권을 2042�까지 연장합니�.
회사� gedatolisib 특허 포트폴리오는 현재 미국 특허 13�� 해외 특허 290�� 포함하며, 조성�, 제형 � 사용 방법� 포괄합니�. Celcuity� 2025� 3분기� PIK3CA 야생� 코호트에 대� VIKTORIA-1 임상시험� 주요 데이터를, 2025� 4분기에는 PIK3CA 돌연변� 코호� 데이터를 발표� 예정입니�.
Celcuity (Nasdaq : CELC) a obtenu un nouveau brevet américain (n° 12 350 276) pour le schéma posologique clinique de gedatolisib, son principal candidat médicament pour les patientes atteintes d'un cancer du sein ER+/HER2-. Ce brevet prolonge l'exclusivité de la société jusqu'en 2042.
Le portefeuille de brevets de gedatolisib comprend désormais 13 brevets américains et 290 brevets étrangers, couvrant la composition, les formulations et les méthodes d'utilisation. Celcuity prévoit de publier les données principales de l'essai clinique VIKTORIA-1 pour la cohorte PIK3CA de type sauvage au 3e trimestre 2025 et pour la cohorte mutante PIK3CA au 4e trimestre 2025.
Celcuity (Nasdaq: CELC) hat ein neues US-Patent (Nr. 12.350.276) für das klinische Dosierungsschema von gedatolisib erhalten, dem führenden Arzneimittelkandidaten für ER+/HER2- Brustkrebspatienten. Dieses Patent verlängert die Exklusivität des Unternehmens bis 2042.
Das Patentportfolio von gedatolisib umfasst nun 13 US-Patente und 290 ausländische Patente, die Zusammensetzung, Formulierungen und Anwendungsweisen abdecken. Celcuity plant, die Topline-Daten der VIKTORIA-1-Studie für die PIK3CA Wildtyp-Kohorte im 3. Quartal 2025 und für die PIK3CA Mutanten-Kohorte im 4. Quartal 2025 zu veröffentlichen.
- Patent protection for gedatolisib extended until 2042, ensuring long-term market exclusivity
- Robust patent portfolio with 13 U.S. patents and 290 foreign patents
- Clinical trial results for two cohorts expected within 2025
- None.
MINNEAPOLIS, July 14, 2025 (GLOBE NEWSWIRE) -- Celcuity Inc. (Nasdaq: CELC), a clinical-stage biotechnology company pursuing development of targeted therapies for oncology, today announced the issuance of U.S. Patent No. 12,350,276 covering the clinical dosing regimen for its lead drug candidate, gedatolisib, in ER+/HER2- breast cancer patients. The patent extends Celcuity’s patent exclusivity in the U.S. into 2042.
“This dosing regimen patent reflects our commitment to enhancing our intellectual property portfolio,� said Brian Sullivan, CEO and Co-Founder of Celcuity. “With patent exclusivity for gedatolisib now extended into 2042, we expect to have a long runway to optimize development of gedatolisib.�
The United States Patent and Trademark Office previously issued five U.S. patents directed to gedatolisib’s composition of matter, four U.S. patents directed to various formulations comprising gedatolisib, and three U.S. patents directed to methods of using gedatolisib. The worldwide gedatolisib-related patent portfolio now comprises 13 granted gedatolisib-related patents in the U.S. and 290 patents granted in foreign jurisdictions.
Celcuity expects to announce topline data for the PIK3CA wild-type cohort of the VIKTORIA-1 clinical trial in the third quarter of 2025 and to report topline data for the PIK3CA mutant cohort in the fourth quarter of 2025.
About Celcuity
Celcuity is a clinical-stage biotechnology company pursuing development of targeted therapies for 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 is currently enrolling patients. 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. A Phase 3 clinical trial, VIKTORIA-2, evaluating gedatolisib plus a CDK4/6 inhibitor and fulvestrant as first-line treatment for patients with HR+/HER2- advanced breast cancer is currently recruiting patients. More detailed information about Celcuity’s active clinical trials can be found at . Celcuity is headquartered in Minneapolis. Further information about Celcuity can be found at . Follow us on Ի.
Forward-Looking Statements
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements relating to patent scope and length of protection and the anticipated timing of topline data from the VIKTORIA-1 clinical trial. Words such as, but not limited to, “look forward to,� “believe,� “expect,� “anticipate,� “estimate,� “intend,� "confidence," "encouraged," “potential,� “plan,� “targets,� “likely,� “may,� “will,� “would,� “should� and “could,� and similar expressions or words identify forward-looking statements. The forward-looking statements included in this press release are based on management's current expectations and beliefs which are subject to a number of risks, uncertainties and factors, including that generics or others could challenge the validity of the gedatolisib patents, Celcuity may not be able to enforce the patents, there could be patent-related litigation or the progress of the VIKTORIA-1 clinical trial may be delayed. In addition, all forward-looking statements are subject to other risks detailed in our Annual Report on Form 10-K for the year ended December 31, 2024. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. All forward-looking statements are qualified in their entirety by these cautionary statements, and we undertake no obligation to revise or update this news release to reflect events or circumstances after the date hereof.
Contacts:
Celcuity Inc.
Brian Sullivan,
Vicky Hahne,
(763) 392-0123
ICR Healthcare
Patti Bank, [email protected]
(415) 513-1284
