SOUTH SAN FRANCISCO, CA -- (Marketwire) -- 08/24/09 -- Cytokinetics, Incorporated (NASDAQ: CYTK) announced today that data relating to two Phase IIa clinical trials
evaluating omecamtiv mecarbil (formerly CK-1827452), one in stable heart
failure patients and one in patients with ischemic cardiomyopathy and
angina, are scheduled to be presented in two poster presentations at the
European Society of Cardiology Congress 2009, to be held August 29 -
September 2, 2009 at the Fira Gran Via Plaza Europa in Barcelona, Spain.
Poster Presentations
Abstract #84776: "Echocardiographic Detection of Increases in Ejection
Fraction in Patients with Heart Failure Receiving the Selective Cardiac
Myosin Activator, CK-1827452" is scheduled to be displayed on Monday,
August 31, 2009 from 8:30 AM - 12:30 PM Central European Summer Time
(CEST) in Zone 3. The poster will be moderated by Andrew Wolff, MD, FACC,
Senior Vice President of Clinical Research and Development and Chief
Medical Officer, Cytokinetics, Inc., South San Francisco, California.
Abstract #84636: "Phase II Safety Study Evaluating the Novel Cardiac
Myosin Activator, CK-1827452, in Patients with Ischemic Cardiomyopathy and
Angina" is scheduled to be displayed on Monday, August 31, 2009 from 8:30
AM - 12:30 PM CEST in Zone 3. The poster will be moderated by Barry H.
Greenberg, MD, Director, Advanced Heart Failure Treatment Program,
University of California, San Diego Medical Center and Chair of the Safety
Review Committee for this clinical trial.
About Cytokinetics
Cytokinetics is a clinical-stage biopharmaceutical company focused on the
discovery and development of novel small molecule therapeutics that
modulate muscle function for the potential treatment of serious diseases
and medical conditions. Cytokinetics' cardiac muscle contractility program
is focused on cardiac muscle myosin, a motor protein essential to cardiac
muscle contraction. Cytokinetics' lead compound from this program,
omecamtiv mecarbil (formerly CK-1827452), a novel small molecule cardiac
muscle myosin activator, is in Phase II clinical trials for the potential
treatment of heart failure. In May 2009, Amgen Inc. exercised an option to
obtain an exclusive worldwide (excluding Japan) license to develop and
commercialize omecamtiv mecarbil and related compounds. Under the terms
of the companies' agreement, Amgen has assumed responsibility for
development and commercialization of omecamtiv mecarbil and related
compounds, at its expense, subject to specified development and
commercialization participation rights of Cytokinetics. In June 2009,
Cytokinetics initiated a Phase I clinical trial of CK-2017357, a fast
skeletal muscle troponin activator, in healthy volunteers in the United
States.