- Company to Host Conference Call at 4:30 p.m. ET Today -
SUNNYVALE, Calif., Aug. 14 /PRNewswire-FirstCall/ -- Pharmacyclics, Inc. (Nasdaq: PCYC) today reported financial results for its fourth quarter and fiscal year ended June 30, 2008. The net loss for the fourth quarter of fiscal 2008 was $4.6 million, or $0.18 per share, compared to a net loss of $7.0 million, or $0.27 per share, for the fourth quarter of fiscal 2007.
Total operating expenses were $4.8 million for the fourth quarter of fiscal 2008 compared to $7.6 million for the fourth quarter of fiscal 2007. Share-based compensation expense was $0.5 million in the fourth quarter of fiscal 2008 compared to $0.8 million in the fourth quarter of fiscal 2007. The decrease in total operating expenses in the fourth quarter of fiscal 2008 was primarily related to reduced personnel expenses due to lower headcount, lower outside clinical trial costs and reduced preclinical expenses associated with the company's Factor VIIa inhibitor program due to the completion of preclinical activities.
Pharmacyclics also reported financial results for the fiscal year ended June 30, 2008. The net loss for the fiscal year ended June 30, 2008 was $24.3 million, or $0.93 per share. This compares to a net loss of $26.2 million, or $1.08 per share, for fiscal year 2007.
As of June 30, 2008, the company had cash, cash equivalents and marketable securities totaling $16.8 million. This compares to $38.8 million in cash, cash equivalents and marketable securities as of June 30, 2007.
Fiscal 2009 Guidance
Pharmacyclics projects total operating expenses, excluding share-based compensation, of between $14 and $15 million for fiscal year 2009, including general and administrative expenses of approximately $4 million. Including share-based compensation expense, Pharmacyclics projects total operating expenses of between $16 and $17 million for fiscal year 2009, including general and administrative expenses of approximately $5 million. Financial projections involve a high level of uncertainty due to, among other factors, the variability involved in predicting requirements of early stage research programs and clinical trials, the potential for entering into partnering arrangements or strategic collaborations, the timing of U.S. Food and Drug Administration (FDA) decisions and share-based compensation expense.
"We continue to advance our pipeline of novel product candidates with
our HDAC inhibitor moving into a Phase 2 trial for treatment of lymphomas
and the filing of an IND for our Factor VIIa inhibitor," said Richard A.
Miller, M.D., president and chief executive officer of Pharmacyclics.
"Enrollment in two Phase 2 trials with motexafin gadolinium for adult brain
tumors and childhood gliomas also continues under sponsorship of the
National Cancer Institute and we are planning to conduct a pivotal Phase 3
trial with motexafin gadolinium in patients with brain metastases from lung
cancer. Our strategy is to build value in these multiple products as we
progress with their development."
Recent and Upcoming Milestones
* Initiated a multicenter Phase 2 trial evaluating oral HDAC
inhibitor, PCI-24781, in hematologic malignancies.
* Announced final data from a Phase 1/2 study showing a 46 percent
complete response rate and a 57 percent overall response rate in 28
patients with multiply recurrent non-Hodgkin's lymphoma (NHL) who
were treated with motexafin gadolinium (MGd, Xcytrin(R)) in
combination with Yttrium-90 Ibritumomab Tiuxetan (Zevalin(TM)), an
approved antibody-targeted radiation therapy.
* Announced results from a preclinical study evaluating PCI-32765, an
orally available, selective inhibitor of Bruton's tyrosine kinase,
or Btk, in collagen induced arthritis, an established animal model
for rheumatoid arthritis (RA). Treatment of animals with advanced
disease, with PCI-32765 reduced inflammation and induced regression
* Filed an investigational new drug (IND) application for PCI-27483, a
small molecule inhibitor of Factor VIIa being developed both for the
treatment of thrombotic complications of cancer and as an
* Plan to complete enrollment and evaluation of a Phase 1 trial in
normal volunteers with our Factor VIIa inhibitor, PCI-27483, in the
fourth quarter of calendar 2008.
* Plan to initiate a Phase 1 trial with our oral Btk inhibitor,
PCI-32765, in patients with recurrent B-cell lymphoma in the fourth
quarter of calendar 2008. This study is designed to evaluate safety
and efficacy using a novel pharmacodynamic biomarker.
* Plans are underway to design and conduct a pivotal Phase 3 trial
with motexafin gadolinium in patients with brain metastases from
non-small cell lung cancer receiving whole brain radiation and
stereotactic radiosurgery. This trial is anticipated to begin in the
first half of calendar 2009.
Conference Call and Webcast Details
The Company will hold a conference call today at 4:30 p.m. EDT to discuss fiscal 2008 year-end financial results and achievements and fiscal 2009 guidance. To participate in the conference call, please dial 800-497-0451 for domestic callers and 706-758-3306 for international callers and reference conference passcode 59146626. To access the live audio broadcast or the subsequent archived recording, log on to http://www.pharmacyclics.com. The archived version of the webcast will be available on the company's website for one month.
Pharmacyclics is a pharmaceutical company developing innovative products to treat cancer and other serious diseases. The company is leveraging its small-molecule drug development expertise to build a pipeline in oncology and immune diseases based on a wide range of targets, pathways and mechanisms. More information about the company, its technology, and products can be found at http://www.pharmacyclics.com. Pharmacyclics(R), Xcytrin(R) and the "pentadentate" logo(R) are registered trademarks of Pharmacyclics, Inc.
NOTE: Other than statements of historical fact, the statements made in
this press release about projected operating expenses, plans for initiating
Phase 1 trials for PCI-27483 and PCI-32765, plans to conduct a pivotal
Phase 3 trial for motexafin gadolinium, and other future plans and
timelines for our preclinical studies and clinical trials, progress of and
reports of results from preclinical studies and clinical trials, clinical
development plans and product development and corporate partnering
activities are forward-looking statements, as defined in the Private
Securities Litigation Reform Act of 1995. The words "project," "believe,"
"will," "may," "continue," "plan," "expect," "intend," "anticipate,"
variations of such words, and similar expressions also identify
forward-looking statements, but their absence does not mean that the
statement is not forward-looking. The forward-looking statements are not
guarantees of future performance and are subject to risks and uncertainties
that may cause actual results to differ materially from those in the
forward-looking statements. Factors that could affect actual results
include risks associated with unexpected delays in clinical trials and
preclinical studies and the timing for making related regulatory filings;
our ability to estimate accurately the amount of cash to be used to fund
operations over the next 12 months, our ability to obtain future financing
and fund the product development of our pipeline; the fact that data from
preclinical studies and Phase 1 or Phase 2 clinical trials may not
necessarily be indicative of future clinical trial results; the initiation,
timing, design, enrollment and cost of clinical trials and preclinical
studies; our ability to establish successful partnerships and
collaborations with third parties; the regulatory approval process in the
United States and other countries; and our future capital requirements. For
further information about these risks and other factors that may affect the
actual results achieved by Pharmacyclics, please see the company's reports
as filed with the U.S. Securities and Exchange Commission from time to
time, including but not limited to its annual report on Form 10-K for the
period ended June 30, 2007 and its subsequently filed quarterly reports on
Form 10-Q. Forward-looking statements contained in this announcement are
made as of this date, and we undertake no obligation to publicly update any
forward-looking statement, whether as a result of new information, future
events or otherwise.
(a development stage enterprise)
Condensed Statements of Operations
(unaudited) (in thousands, except per share data)
Three Months Twelve Months
Ended June 30, Ended June 30,
2008 2007 2008 2007
Grant revenue $-- $107 $-- $126
Research and development 3,358 5,558 18,180 21,115
General and administrative 1,409 2,088 7,332 7,403
Total operating expenses 4,767 7,646 25,512 28,518
Loss from operations (4,767) (7,539) (25,512) (28,392)
Interest and other, net 139 549 1,214 2,175
Net loss $(4,628) $(6,990) $(24,298) $(26,217)
Basic and diluted net loss per share $(0.18) $(0.27) $(0.93) $(1.08)
Shares used to compute basic and
diluted net loss per share 26,008 25,958 25,989 24,175
Condensed Balance Sheets
(unaudited, in thousands)
June 30, June 30,
Cash, cash equivalents and marketable
securities $16,755 $38,762
Other current assets 401 961
Total current assets 17,156 39,723
Property and equipment, net 688 849
Other noncurrent assets 523 523
Liabilities and stockholders' equity
Current liabilities $1,851 $2,615
Long-term obligations 71 79
Stockholder's equity 16,445 38,401
|SOURCE Pharmacyclics, Inc.|
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