Cytokinetics Announces Two Presentations at the 2024 American College of Clinical Pharmacology Annual Meeting
Cytokinetics (Nasdaq: CYTK) has announced two presentations at the 2024 American College of Clinical Pharmacology (ACCP) Annual Meeting in Bethesda, MD, scheduled from September 8-10, 2024. The first presentation, titled 'A First-in-Human, Single & Multiple Ascending Dose Study of CK-4021586, A Novel Cardiac Myosin Inhibitor', will be presented by Justin Lutz, Senior Director of Clinical Pharmacology. The second presentation, 'Clinical Evaluation of the Effect of Aficamten on QT/QTc Interval in Healthy Participants', will be delivered by Polina German, Executive Director of Clinical Pharmacology. Both presentations are scheduled for September 8, 2024, during the Opening Reception, Exhibits & Poster Session 1, from 5:00-7:00 PM ET in the Grand Ballroom E-H.
Cytokinetics (Nasdaq: CYTK) ha annunciato due presentazioni alla Riunione Annuale del 2024 del Collegho Americano di Farmacologia Clinica (ACCP) che si terrà a Bethesda, MD, dal 8 al 10 settembre 2024. La prima presentazione, intitolata 'Uno Studio Prima nell'Uomo, a Dosi Singole e Multiple Crescenti di CK-4021586, un Nuovo Inibitore della Miosina Cardiacà', sarà presentata da Justin Lutz, Direttore Senior di Farmacologia Clinica. La seconda presentazione, 'Valutazione Clinica dell'Effetto di Aficamten sull'Intervallo QT/QTc in Partecipanti Sani', sarà tenuta da Polina German, Direttrice Esecutiva di Farmacologia Clinica. Entrambe le presentazioni sono programmate per il 8 settembre 2024, durante la Ricezione di Apertura, Mostre e Sessione Poster 1, dalle 17:00 alle 19:00 ET nella Grand Ballroom E-H.
Cytokinetics (Nasdaq: CYTK) ha anunciado dos presentaciones en la Reunión Anual 2024 del Colegio Americano de Farmacología Clínica (ACCP) que se llevará a cabo en Bethesda, MD, del 8 al 10 de septiembre de 2024. La primera presentación, titulada 'Un Estudio Primero en Humanos, de Dosis Únicas y Múltiples Ascendentes de CK-4021586, un Nuevo Inhibidor de Miosina Cardíaca', será presentada por Justin Lutz, Director Senior de Farmacología Clínica. La segunda presentación, 'Evaluación Clínica del Efecto de Aficamten en el Intervalo QT/QTc en Participantes Sanos', será entregada por Polina German, Directora Ejecutiva de Farmacología Clínica. Ambas presentaciones están programadas para el 8 de septiembre de 2024, durante la Recepción de Apertura, Exposiciones y Sesión de Pósters 1, de 5:00 a 7:00 PM ET en el Grand Ballroom E-H.
Cytokinetics (Nasdaq: CYTK)는 2024년 9월 8일부터 10일까지 메릴랜드주 베서다에서 열리는 미국 임상 약리학회(ACCP) 연례 회의에서 두 가지 발표를 발표했습니다. 첫 번째 발표는 'CK-4021586의 사람을 대상으로 한 최초의 단일 및 반복 상승 용량 연구, 새로운 심장 미오신 억제제'라는 제목으로, 세니어 임상 약리학 이사인 저스틴 루츠가 발표합니다. 두 번째 발표인 '건강한 참가자에서 Aficamten의 QT/QTc 간격에 대한 임상 평가'는 임상 약리학 전무 이사인 폴리나 게르만이 전달합니다. 두 발표 모두 2024년 9월 8일 개회 리셉션, 전시 및 포스터 세션 1 중 오후 5시부터 7시까지 ET에 그랜드 볼룸 E-H에서 진행될 예정입니다.
Cytokinetics (Nasdaq: CYTK) a annoncé deux présentations lors de la Réunion Annuelle 2024 du Collège Américain de Pharmacologie Clinique (ACCP) prévue à Bethesda, MD, du 8 au 10 septembre 2024. La première présentation, intitulée 'Une Étude de Première Administration à l'Homme, à Doses Simples et Multiples Ascendantes de CK-4021586, un Nouvel Inhibiteur de Myosine Cardiaque', sera présentée par Justin Lutz, Directeur Senior de la Pharmacologie Clinique. La deuxième présentation, 'Évaluation Clinique de l'Effet d'Aficamten sur l'Intervalle QT/QTc chez des Participants Sains', sera faite par Polina German, Directrice Exécutive de la Pharmacologie Clinique. Les deux présentations sont programmées pour le 8 septembre 2024, lors de la Réception d'Ouverture, des Expositions et de la Session des Posters 1, de 17h00 à 19h00 ET dans le Grand Ballroom E-H.
Cytokinetics (Nasdaq: CYTK) hat zwei Präsentationen auf dem 2024 American College of Clinical Pharmacology (ACCP) Annual Meeting in Bethesda, MD, angekündigt, das vom 8. bis 10. September 2024 stattfindet. Die erste Präsentation mit dem Titel 'Eine Erste-in-Menschen-Studie mit Einmal- und Mehrfachdosen von CK-4021586, einem neuartigen Inhibitor der Herzmyosine' wird von Justin Lutz, Senior Director der Klinischen Pharmakologie, gehalten. Die zweite Präsentation, 'Klinische Bewertung der Wirkung von Aficamten auf das QT/QTc-Intervall bei gesunden Teilnehmern', wird von Polina German, Executive Director der Klinischen Pharmakologie, geliefert. Beide Präsentationen sind für den 8. September 2024 während der Eröffnungsrezeption, Ausstellungen und Poster-Sitzung 1 von 17:00 bis 19:00 Uhr ET im Grand Ballroom E-H geplant.
- Presentation of full data from Phase 1 study of CK-4021586, a novel cardiac myosin inhibitor
- Clinical evaluation results of Aficamten's effect on QT/QTc interval in healthy participants
- None.
Full Data from Phase 1 Study of CK-4021586 to be Presented on September 8, 2024
SOUTH SAN FRANCISCO, Calif., Sept. 05, 2024 (GLOBE NEWSWIRE) -- Cytokinetics, Incorporated (Nasdaq: CYTK) today announced two presentations at the 2024 American College of Clinical Pharmacology (ACCP) Annual Meeting in Bethesda, MD from September 8, 2024 – September 10, 2024.
Title: A First-in-Human, Single & Multiple Ascending Dose Study of CK-4021586, A Novel Cardiac Myosin Inhibitor
Presenter: Justin Lutz, Pharm. D., Ph.D., Senior Director, Clinical Pharmacology, Cytokinetics
Date: September 8, 2024
Session Title: Opening Reception, Exhibits & Poster Session 1
Topic: Pharmacokinetics (Including PopPK, ADME, Biopharmaceutics)
Poster Number: 074
Session Time: 5:00-7:00 PM ET
Location: Grand Ballroom E-H
Title: Clinical Evaluation of the Effect of Aficamten on QT/QTc Interval in Healthy Participants
Presenter: Polina German, Pharm. D., Executive Director, Clinical Pharmacology, Cytokinetics
Date: September 8, 2024
Session Title: Opening Reception, Exhibits & Poster Session 1
Topic: General Drug Development Strategy & Practice
Poster Number: 022
Session Time: 5:00-7:00 PM ET
Location: Grand Ballroom E-H
About Cytokinetics
Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing muscle biology-directed drug candidates as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. Cytokinetics is preparing for regulatory submissions for aficamten, its next-in-class cardiac myosin inhibitor, following positive results from SEQUOIA-HCM, the pivotal Phase 3 clinical trial in obstructive hypertrophic cardiomyopathy which were published in the New England Journal of Medicine. Aficamten is also currently being evaluated in MAPLE-HCM, a Phase 3 clinical trial of aficamten as monotherapy compared to metoprolol as monotherapy in patients with obstructive HCM, ACACIA-HCM, a Phase 3 clinical trial of aficamten in patients with non-obstructive HCM, CEDAR-HCM, a clinical trial of aficamten in a pediatric population with obstructive HCM, and FOREST-HCM, an open-label extension clinical study of aficamten in patients with HCM. Cytokinetics is also developing omecamtiv mecarbil, a cardiac muscle activator, in patients with heart failure. Additionally, Cytokinetics is developing CK-586, a cardiac myosin inhibitor with a mechanism of action distinct from aficamten for the potential treatment of HFpEF.
For additional information about Cytokinetics, visit www.cytokinetics.com and follow us on X, LinkedIn, Facebook and YouTube.
Forward-Looking Statements
This press release contains forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995 (the "Act"). Cytokinetics disclaims any intent or obligation to update these forward-looking statements and claims the protection of the Act's Safe Harbor for forward-looking statements. Examples of such statements include, but are not limited to, statements relating to any of our other clinical trials, statements relating to the potential benefits of aficamten, CK-586 or any of our other drug candidates. Cytokinetics' research and development activities; the design, timing, results, significance and utility of preclinical and clinical results; and the properties and potential benefits of Cytokinetics' other drug candidates. Such statements are based on management's current expectations, but actual results may differ materially due to various risks and uncertainties, including, but not limited to, potential difficulties or delays in the development, testing, regulatory approvals for trial commencement, progression or product sale or manufacturing, or production of Cytokinetics' drug candidates that could slow or prevent clinical development or product approval; Cytokinetics' drug candidates may have adverse side effects or inadequate therapeutic efficacy; the FDA or foreign regulatory agencies may delay or limit Cytokinetics' ability to conduct clinical trials; Cytokinetics may be unable to obtain or maintain patent or trade secret protection for its intellectual property; standards of care may change, rendering Cytokinetics' drug candidates obsolete; and competitive products or alternative therapies may be developed by others for the treatment of indications Cytokinetics' drug candidates and potential drug candidates may target. For further information regarding these and other risks related to Cytokinetics' business, investors should consult Cytokinetics' filings with the Securities and Exchange Commission.
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Contact:
Cytokinetics
Diane Weiser
Senior Vice President, Corporate Affairs
(415) 290-7757
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