SOUTH SAN FRANCISCO, CA--(Marketwire - February 10, 2009) -
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"In the fourth quarter we were encouraged by data arising from our Phase IIa clinical trials in heart failure for our lead drug candidate CK-1827452. In particular, we believe the top-line results from our Phase IIa trial evaluating CK-1827452 in heart failure patients with ischemic cardiomyopathy and angina support the safety of this novel cardiac myosin activator in a high-risk heart failure patient population," stated Robert I. Blum, Cytokinetics' President and Chief Executive Officer. "More recently, we announced the extension and expansion of our development pipeline focused on the modulation of muscle contractility, with the progression of CK-2017357, our novel skeletal muscle activator, in IND-enabling studies and the designation of two additional potential drug candidates arising from our ongoing research activities."
Company Highlights
Cardiovascular
-- In December, Cytokinetics announced top-line results from a Phase IIa
clinical trial evaluating the safety of CK-1827452 in patients with
ischemic cardiomyopathy and angina. The primary safety endpoint was defined
as stopping an exercise test during double-blind treatment with CK-1827452
or placebo due to unacceptable angina at an earlier exercise stage than at
baseline. This endpoint was observed in one patient receiving placebo and
did not occur in any patient receiving CK-1827452. The company believes
that the results from this safety trial support the progression of CK-
1827452 into Phase IIb development.
-- In November, at the 2008 Scientific Sessions of the American Heart
Association, Cytokinetics reported interim results from an ongoing Phase
IIa clinical trial evaluating CK-1827452 administered intravenously to
patients with stable heart failure. The interim results showed that CK-
1827452 demonstrated statistically significant increases in systolic
ejection time and fractional shortening at plasma concentrations greater
than 100 ng/mL, statistically significant increases in stroke volume at
plasma concentrations greater than 200 ng/mL, and statistically significant
increases in ejection fraction at plasma concentrations greater than 300
ng/mL. In addition, these data demonstrated statistically significant
correlations between increasing CK-1827452 plasma concentration and
increases in systolic ejection time, stroke volume, and fractional
shortening, ejection fraction and cardiac output. The results also showed
statistically significant correlations between increasing CK-1827452
concentrations and decreases in supine and standing heart rate and left
ventricular end-systolic volume. Cytokinetics recently completed dosing in
the fifth cohort of this trial.
-- Cytokinetics continues to enroll and dose patients in an ongoing Phase
IIa trial to evaluate an intravenous formulation of CK-1827452 in patients
with stable heart failure undergoing clinically indicated coronary
angiography in the cardiac catheterization laboratory.
-- In December, Cytokinetics provided an update on a recently completed
Phase I clinical trial of CK-1827452 designed to evaluate the potential for
certain drug-drug interactions mediated by two cytochrome P450 drug-
metabolizing enzymes, 2D6 and 3A4. Results showed that there were no
clinically important differences observed between extensive or poor
metabolizers via 2D6 in the pharmacokinetics of CK-1827452. Furthermore no
clinically meaningful drug-drug interactions were identified with either
ketoconazole or diltiazem (a potent and a moderate inhibitor of 3A4,
respectively) in either extensive or poor metabolizers via 2D6.
Oncology
-- In December, at the 31st Annual San Antonio Breast Cancer Symposium,
Cytokinetics presented a clinical poster summarizing interim data from the
Phase I portion of a Phase I/II clinical trial evaluating ispinesib in the
treatment of women with locally advanced or metastatic breast cancer.
Cytokinetics continues to enroll and dose-escalate patients in the Phase I
portion of this trial.
-- In December, at the 2008 Annual Meeting of the American Society of
Hematology, interim data from the Phase I portion of a Phase I/II clinical
trial evaluating SB-743921 in patients with Hodgkin or non-Hodgkin lymphoma
were presented. Cytokinetics continues to enroll and dose-escalate patients
in the Phase I portion of this trial.
-- GlaxoSmithKline (GSK) continues to enroll and dose-escalate patients
in a Phase I first-in-humans clinical trial evaluating GSK-923295, an
inhibitor of centromere-associated protein E (CENP-E), in patients with
advanced solid tumors.
Non-Clinical Research and Development
-- In January 2009, Cytokinetics announced updates relating to its
internal programs directed to muscle biology. The company announced that it
plans to submit an investigational new drug application (IND) in 2009 for
CK-2017357, a skeletal muscle activator, which had been selected for
development in April 2008. This compound is the lead potential drug
candidate arising from the company's skeletal muscle activator research
program. The company also announced that is has recently designated a
second skeletal muscle activator from this research program for
development. In addition, Cytokinetics announced the selection of a small
molecule inhibitor of smooth muscle myosin for development. This potential
drug candidate is expected to enter IND-enabling studies in 2009.
Corporate
-- In December, GSK informed Cytokinetics that it would not exercise its
option to license ispinesib or SB-743921 as provided under the companies'
collaboration and license agreement. As a result, all rights to ispinesib
and SB-743921, each novel inhibitors of kinesin spindle protein, remain
with Cytokinetics, on agreed terms. The collaboration between Cytokinetics
and GSK is continuing with a focus on GSK-923295 and translational research
related to CENP-E.
-- In October, Cytokinetics accepted an offer of settlement with UBS AG
relating to certain auction rate securities (ARS). Pursuant to the
settlement, UBS AG has issued to Cytokinetics Series C-2 Auction Rate
Securities Rights, which provide the company the right to cause UBS to
purchase these ARS at par value at any time between June 30, 2010 and July
2, 2012. In addition, UBS may elect to purchase some or all of the ARS at
par value at anytime prior to June 30, 2010. In connection with the
settlement, Cytokinetics entered into a no net cost loan agreement with UBS
Bank USA and UBS Financial Services Inc., and on January 5, 2009 borrowed
approximately $12.4 million under the loan agreement, with the company's
ARS held in accounts with UBS and its affiliates as collateral.
Financials
Revenues from research and development collaborations for the fourth quarter of 2008 were $3.2 million, compared to $3.1 million for the same period in 2007. Revenues for the fourth quarter of 2008 and 2007 were primarily derived from the company's collaboration and option agreement with Amgen, Inc.
Total research and development (R&D) expenses in the fourth quarter of 2008 were $11.5 million, compared to $14.0 million for the same period in 2007. The decrease in R&D expenses in the fourth quarter of 2008, compared to the same period in 2007, was primarily due to decreased laboratory and personnel expenses, which were partially offset by increased spending related to the company's clinical trial programs.
Total general and administrative (G&A) expenses for the fourth quarter of 2008 were $2.8 million, compared to $4.1 million for the same period in 2007. The decrease in G&A expenses in the fourth quarter of 2008, compared to the same period in 2007, was primarily due to decreased legal fees and personnel expenses.
Cytokinetics also reported results of its operations for the twelve months ended December 31, 2008. Revenues from research and development collaborations for the twelve months ended December 31, 2008 were $12.4 million, compared to revenues of $13.6 million for the same period in 2007. The decrease in collaborative research revenues in 2008, as compared to the same period in 2007, was primarily the result of lower revenue from the company's collaboration with GSK.
Total R&D expenses for the twelve months ended December 31, 2008 were $54.0 million, compared to $53.4 million for the same period in 2007. The increase in R&D expenses in 2008, compared to the same period in 2007, was primarily due to higher clinical trial related costs, which were offset in part by decreased laboratory and personnel expenses.
Total G&A expenses for the twelve months ended December 31, 2008 were $15.1 million, compared to $16.7 million for the same period in 2007. The decreased G&A expenses in 2008, compared to the same period in 2007, was primarily due to decreased legal and personnel expenses.
The net loss for the twelve months ended December 31, 2008, which included $2.5 million in restructuring charges, was $56.4 million, or $1.14 per share, compared to a net loss of $48.9 million, or $1.03 per share, for the same period in 2007.
Company Milestones for 2009
Cardiovascular
CK-1827452
-- In March, Cytokinetics plans to present final data from its ongoing
Phase IIa clinical trial of CK-1827452 in patients with stable heart
failure at the Annual Meeting of the American College of Cardiology in
Orlando, Florida.
-- In 2009, Cytokinetics plans to present final data from its Phase IIa
clinical trial of CK-1827452 in patients with ischemic cardiomyopathy and
angina.
-- In mid-2009, Cytokinetics anticipates the initiation of a Phase IIb
clinical trial of CK-1827452 in chronic heart failure outpatients at
increased risk for death and hospitalization.
Oncology
GSK-923295
-- In 2009, Cytokinetics anticipates that GSK will initiate a Phase II
clinical trial of GSK-923295.
Non-Clinical Research and Development
-- In 2009, Cytokinetics plans to submit an IND application relating to
CK-2017357 and to initiate a Phase I study of CK-2017357 in healthy
volunteers.
-- In 2009, Cytokinetics anticipates progressing its smooth muscle myosin
inhibitor in IND-enabling studies.
Corporate
-- In the first quarter of 2009, Cytokinetics anticipates providing the
required clinical data from its CK-1827452 Phase IIa clinical trials
program to Amgen in order to inform the potential exercise of Amgen's
option under the companies' strategic alliance.
Financial Guidance for 2009
Cytokinetics also announced its financial guidance for 2009. The company anticipates its 2009 net cash utilization to be in the range of $52.0 to $57.0 million, with cash R&D expenses expected to be in the range of $38.0 to $42.0 million and cash G&A expenses to be in the range of $14.0 to $15.0 million. On this basis, the company believes that it has over 12 months of cash resources to fund operations.
While Amgen may choose to exercise its option for an exclusive license to develop and commercialize CK-1827452, there is no certainty this will occur. Accordingly, this financial guidance excludes any revenues associated with such an option exercise by Amgen, including any projections regarding potential reimbursement of R&D expenses related to CK-1827452. This guidance also does not take into account revenues from other potential collaborations that Cytokinetics may enter into in 2009 relating to CK-1827452 or other programs.
If Amgen does exercise its option, Cytokinetics will provide an update to its 2009 financial guidance, taking into account the $50 million option exercise fee that Amgen would pay to the company, as well as any other payments that Cytokinetics may receive from Amgen for R&D activities related to CK-1827452 that it may conduct under Amgen's sponsorship. Cytokinetics expects that if Amgen exercises its option related to CK-1827452, the company's cash resources would be then sufficient for approximately 24 months of operations. This financial guidance is on a cash basis and does not include an estimated $12.0 million in GAAP revenues related to Amgen's initial payment for its option for a license of CK-1827452 and $7.5 million in non-cash related operating expenses primarily related to FAS 123R stock compensation expense.
Annual Stockholders' Meeting
Cytokinetics' Annual Stockholders' Meeting will be held at the Embassy Suites Hotel located at 250 Gateway Boulevard in South San Francisco, CA at 10:00 AM on May 21, 2009.
Conference Call and Webcast Information
Members of Cytokinetics' management team will review fourth quarter and year end results via a webcast and conference call today at 4:30 PM Eastern Time. The webcast can be accessed in the Investor Relations section of Cytokinetics' website at www.cytokinetics.com. The live audio of the conference call is also accessible via telephone to investors, members of the news media and the general public by dialing either (866) 999-CYTK (2985) (United States and Canada) or (706) 679-3078 (International) and typing in the passcode 81393620.
An archived replay of the webcast will be available via Cytokinetics' website until February 24, 2009. The replay will also be available via telephone by dialing (800) 642-1687 (United States and Canada) or (706) 645-9291 (International) and typing in the passcode 81393620 from February 10, 2009 at 5:30 PM Eastern Time until February 24, 2009.
About Cytokinetics
Cytokinetics is a biopharmaceutical company with a focus on muscle contractility that engages in the discovery, development and commercialization of novel small molecule drugs that may address areas of significant unmet clinical needs. Cytokinetics' cardiovascular disease program is focused on cardiac myosin, a motor protein essential to cardiac muscle contraction. Cytokinetics' lead compound from this program, CK-1827452, a novel small molecule cardiac myosin activator, is in Phase II clinical trials for the treatment of heart failure. Amgen Inc. has obtained an option for an exclusive license to develop and commercialize CK-1827452, subject to Cytokinetics' development and commercial participation rights. In April 2008, Cytokinetics announced the selection of a potential drug candidate, CK-2017357, directed towards skeletal muscle contractility which may be developed as a potential treatment for skeletal muscle weakness associated with neuromuscular diseases or other conditions. In January 2009, Cytokinetics announced the selection of a potential drug candidate directed towards smooth muscle contractility which may be developed as a potential treatment for diseases associated with bronchoconstriction and vasoconstriction.
Cytokinetics' cancer program is focused on mitotic kinesins, a family of motor proteins essential to cell division. Cytokinetics is developing two drug candidates that have arisen from this program, ispinesib and SB-743921, each an inhibitor of kinesin spindle protein, a mitotic kinesin. In addition, Cytokinetics and GlaxoSmithKline are conducting research and development activities focused on GSK-923295, an inhibitor of centromere-associated protein E (CENP-E).
All of these drug candidates and potential drug candidates have arisen from Cytokinetics' research activities and are directed towards the cytoskeleton. The cytoskeleton is a complex biological infrastructure that plays a fundamental role within every human cell. Additional information about Cytokinetics can be obtained at www.cytokinetics.com.
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 Amgen's potential exercise of its option to CK-1827452; Cytokinetics' financial guidance, including expected cash operating expenditures, revenues and R&D and G&A expenses for 2009; Cytokinetics' and its partners' research and development activities, including the initiation, conduct, focus, scope and completion of clinical trials, the utility of clinical trial results, the anticipated availability and presentation of clinical trial results, the initiation and progression of IND-enabling studies and the timing and occurrence of IND filings; the potential receipt of payments under Cytokinetics' strategic alliance with Amgen; potential future collaborations; and the properties and potential benefits of Cytokinetics' compounds. 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 production of Cytokinetics' compounds that could slow or prevent clinical development or product approval, including risks that current and past results of clinical trials or preclinical studies may not be indicative of future clinical trials results, patient enrollment for or conduct of clinical trials may be difficult or delayed, Cytokinetics' compounds may have adverse side effects or inadequate therapeutic efficacy, the U.S. Food and Drug Administration or foreign regulatory agencies may delay or limit Cytokinetics' or its partners' ability to conduct clinical trials, and Cytokinetics may be unable to obtain or maintain patent or trade secret protection for its intellectual property; Amgen may elect not to exercise its option with respect to CK-1827452; GSK may alter or terminate its development activities for GSK-923295; Cytokinetics may incur unanticipated research and development and other costs or be unable to obtain the additional funding necessary to conduct development of some or all of its compounds; standards of care may change rendering Cytokinetics' compounds obsolete; others may introduce products or alternative therapies for the treatment of indications Cytokinetics' compounds may target; and risks and uncertainties relating to the timing and receipt of payments from its partners, including option fees, milestones and royalties on future potential product sales under Cytokinetics' collaboration agreements with such partners. For further information regarding these and other risks related to Cytokinetics' business, investors should consult Cytokinetics' filings with the Securities and Exchange Commission.
Condensed Statement of Operations
(in thousands, except share and per share data)
(unaudited)
Three Months Ended Twelve Months Ended
December December December December
31, 31, 31, 31,
2008 2007 2008 2007
---------- ---------- ---------- ----------
Revenues:
Research and development $ 93 $ 51 $ 186 $ 1,388
License revenues 3,058 3,058 12,234 12,234
---------- ---------- ---------- ----------
Total revenues 3,151 3,109 12,420 13,622
---------- ---------- ---------- ----------
Operating Expenses:
Research and development 11,470 13,958 53,950 53,388
General and
administrative 2,841 4,110 15,076 16,721
Restructuring charges (19) - 2,473 -
---------- ---------- ---------- ----------
Total operating
expenses 14,292 18,068 71,499 70,109
---------- ---------- ---------- ----------
Operating loss: (11,141) (14,959) (59,079) (56,487)
Interest and other
income, net 285 1,706 2,705 7,593
---------- ---------- ---------- ----------
Net loss $ (10,856) $ (13,253) $ (56,374) $ (48,894)
========== ========== ========== ==========
Net loss per common share
- basic and diluted $ (0.22) $ (0.27) $ (1.14) $ (1.03)
Weighted average shares
used in computing net
loss per common share
- basic and diluted 49,490,917 49,224,043 49,391,939 47,590,205
Condensed Balance Sheet
(in thousands)
(unaudited)
December 31, December 31,
2008 2007
------------- -------------
Assets
Cash and cash equivalents $ 41,819 $ 116,564
Short term investments 15,048 3,175
Other current assets 2,043 2,277
------------- -------------
Total current assets 58,910 122,016
------------- -------------
Investments in auction rate securities 16,636 20,025
Investment put option 3,389 -
Property and equipment, net 5,087 7,728
Restricted investments 2,750 5,167
Other assets 682 434
------------- -------------
Total assets $ 87,454 $ 155,370
============= =============
Liabilities and stockholders' equity
Current liabilities $ 22,877 $ 26,448
Long-term obligations 14,811 29,006
Stockholders' equity 49,766 99,916
------------- -------------
Total liabilities and stockholders' equity $ 87,454 $ 155,370
============= =============
Cytokinetics, Incorporated
Christopher S. Keenan (Investors and Media)
Director, Investor Relations
(650) 624-3000
