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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): November 2, 2006
NEKTAR THERAPEUTICS
(Exact name of Registrant as specified in its charter)
Delaware 0-24006 94-3134940
(State or other jurisdiction (Commission (IRS Employer
of incorporation) File Number) Identification No.)
150 Industrial Road
San Carlos, California 94070
(Address of principal executive offices and Zip Code)
Registrant's telephone number, including area code: (650) 631-3100
Check the appropriate box below if the Form 8-K filing is intended to
simultaneously satisfy the filing obligation of the registrant under any of the
following provisions:
[ ] Written communications pursuant to Rule 425 under the Securities Act (17
CFR 230.425)
[ ] Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17
CFR 240.14a-12)
[ ] Pre-commencement communications pursuant to Rule 14d-2(b) under the
Exchange Act (17 CFR 240.14d-2(b))
[ ] Pre-commencement communications pursuant to Rule 13e-4(c) under the
Exchange Act (17 CFR 240.13e-4(c))
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Item 2.02 Results of Operations and Financial Condition.
On November 2, 2006, Nektar Therapeutics issued a press release (the "Press
Release") announcing results for the three month and nine month periods ended
September 30, 2006. A copy of the Press Release is attached as Exhibit 99.1 to
this Current Report and is incorporated herein by reference.
The information in this report, including the exhibit hereto, shall not be
deemed "filed" for purposes of Section 18 of the Securities Exchange Act of
1934, as amended, or otherwise subject to the liabilities of that Section or
Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended. The
information contained herein and in the accompanying exhibit shall not be
incorporated by reference into any filing with the Securities and Exchange
Commission made by Nektar Therapeutics, whether made before or after the date
hereof, regardless of any general incorporation language in such filing.
SIGNATURES
Pursuant to the requirement of the Securities Exchange Act of 1934, the
registrant has duly caused this report to be signed on its behalf by the
undersigned thereunto duly authorized.
By: /s/ ROBERT CHESS
--------------------------------
Robert Chess
--------------------------------
Chairman of the Board and Acting
President and Chief Executive
Officer
Date: November 2, 2006
By: /s/ LOUIS DRAPEAU
--------------------------------
Louis Drapeau
--------------------------------
Senior Vice President, Finance
and Chief Financial Officer
Date: November 2, 2006
EXHIBIT INDEX
Exhibit No. Description
- ----------- -----------
99.1 Earnings Press Release of Nektar Therapeutics dated November 2,
2006.
Exhibit 99.1
Nektar Announces Third Quarter 2006 Financial Results
-- Nektar increases revenue estimates and reduces net loss
estimates for full-year 2006; provides preliminary 2007
financial guidance;
-- Exubera(R) (insulin human (rDNA origin)) Inhalation Powder
available in U.S., Germany, U.K. and Ireland;
-- Exubera receives multiple awards for innovation;
-- Nektar pulmonary product (ABIP) for preventing fungal
infections in immunosuppressed patients receives EU orphan
drug designation along with FDA Orphan Drug and Fast Track
designation.
SAN CARLOS, Calif.--(BUSINESS WIRE)--Nov. 2, 2006--Nektar
Therapeutics (Nasdaq:NKTR) announced today its financial results for
the three months ended September 30, 2006.
The company reported total revenue of $58.6 million for the three
months ended September 30, 2006 compared to $36.4 million for the
three months ended September 30, 2005. For the three months ended
September 30, 2006, product sales and royalty revenue was $41.5
million compared to $8.5 million in the three months ended September
30, 2005; and contract revenue totaled $15.1 million compared to $23.7
million in the three months ended September 30, 2005. Exubera product
and royalty revenue for the three months ended September 30, 2006 was
$26.9 million.
Nektar reported a GAAP net loss of $19.6 million or $(0.22) per
share for the three months ended September 30, 2006 compared to a GAAP
net loss of $23.8 million or $(0.28) per share for the three months
ended September 30, 2005.
Nektar also reported a non-GAAP net loss of $14.0 million or
$(0.16) per share for the three months ended September 30, 2006
compared to a non-GAAP net loss for the three months ended September
30, 2005 of $23.8 million or $(0.28) per share. The non-GAAP net loss
for the three months ended September 30, 2006 excludes $2.9 million of
SFAS 123R non-severance stock based compensation charges and $2.7
million of severance and restructuring charges.
For the nine months ended September 30, 2006, Nektar reported
total revenue of $147.8 million compared to total revenue of $93.4
million for the nine months ended September 30, 2005. For the nine
months ended September 30, 2006, product and royalty revenue was $98.0
million compared to $20.3 million for the nine months ended September
30, 2005; and contract research revenue totaled $44.3 million compared
to $62.7 million for the nine months ended September 30, 2005. Exubera
product and royalty revenue for the nine months ended September 30,
2006 was $62.5 million.
For the nine months ended September 30, 2006, Nektar reported a
GAAP net loss of $115.9 or $(1.29) per share compared to a GAAP net
loss for the nine months ended September 30, 2005 of $76.9 million or
$(0.90) per share.
Nektar also reported a non-GAAP net loss for the nine months ended
September 30, 2006 of $63.3 million or $(0.71) per share compared to a
non-GAAP net loss for the nine months ended September 30, 2005 of
$76.9 million or $(0.90) per share.
The non-GAAP net loss for the nine months ended September 30, 2006
excludes $13.3 million of SFAS 123R non-severance stock based
compensation charges, $16.4 million of severance charges, $5.2 million
of restructuring charges related to the closing of Nektar U.K.
(Bradford), and a $17.7 million charge for a litigation settlement
with the University of Alabama Huntsville (UAH). See the supplemental
table attached to this press release entitled "Reconciliation of GAAP
Financial Measures to Non-GAAP Financial Measures."
As of September 30, 2006, Nektar reported cash, cash equivalents,
short-term investments, and investments in marketable securities
totaling approximately $490.9 million compared to $566.4 million as of
December 31, 2005 and $491.1 as of June 30, 2006.
"With the launch underway, orders from Pfizer have increased.
This, combined with our ability to consistently manufacture Exubera
Inhalers and powder at large scale, have enabled us to increase our
revenue estimates for 2006," said Robert Chess, chairman and acting
CEO. "We are pleased that Exubera is now available in the U.S., and
that Pfizer has begun the process of educating leading diabetes care
physicians and health care professionals.
"In addition to Exubera, other aspects of our business are moving
forward. Based on the results of our recent clinical end-of-Phase-2
meeting with the Food and Drug Administration (FDA), we anticipate
moving our inhaled Amphotericin B Inhalation Powder (ABIP) into
pivotal testing in 2007, and we are continuing to advance our other
proprietary products. Further, we are making progress on focusing our
business to achieve profitability and long-term sustainable growth and
meeting or exceeding our financial objectives we have set for the
company in 2006."
Financial Outlook for 2006 and 2007
Today the company is revising its full year 2006 financial
performance estimates and providing preliminary 2007 financial
performance estimates.
2006 Estimates
-- For the full year 2006, Nektar is increasing its total revenue
estimate range to $190 to $210 million from $170 to $200
million, including an increase in estimated Exubera
manufacturing and royalty revenue to $90 to $100 million from
$70 to $90 million, with most of the Exubera related revenue
being generated by manufacturing sales of Exubera to Pfizer.
-- The company is reducing its GAAP net loss estimates to a range
of $155 to $170 million from $160 to $175 million, and
non-GAAP net loss to $95 to $110 million from $100 to $115
million due to increased margins and R&D expenses which are
lower than planned. Non-GAAP net loss excludes the $17.7
million UAH litigation settlement charge, $22 million of
estimated SFAS 123R non-severance stock based compensation
charges, and approximately $20 million of estimated charges
related to restructuring and severance. See the supplemental
table attached to this press release entitled "Reconciliation
of Non-GAAP Projected Financial Guidance for 2006."
-- The company is not changing its estimates of 2006 cash, cash
equivalents, and short-term investments and investments in
marketable securities which remain at an approximate range of
$415 to $440 at the end of the year.
2007 Preliminary Estimates
The company is providing preliminary financial performance
guidance for the full year 2007 as follows:
-- Total revenue for 2007 in the range of $210 to $250 million,
including Exubera revenue of $110 to $130 million, with most
of the estimated Exubera revenue based on estimated
manufacturing sales of Exubera to Pfizer.
-- GAAP net loss of $110 to $130 million.
-- Non-GAAP net loss of $75 to $95 million. Non-GAAP net loss
excludes approximately $35 million of estimated SFAS 123R
stock based compensation charges. See the supplemental table
attached to this press release entitled "Reconciliation of
Non-GAAP Projected Financial Guidance for 2007."
Recent Highlights
Exubera
"As the creator of the core technologies for Exubera, we at Nektar
appreciate the recognition of Exubera for its innovation to bring a
better therapy option to diabetes patients," said Dr. John Patton,
co-founder and chief scientific officer, Nektar.
In September 2006, Exubera received two prestigious awards for
innovation. The Wall Street Journal recognized Exubera first in the
biotechnology and medical category as a technological breakthrough. In
Germany, diabetologists declared Exubera to be the most innovative
diabetes medicine of 2006 as published in trade magazine
"PharmaBarometer."
In early October 2006, Exubera was also awarded the "Best New
Approved Product (Therapeutic)" at the 19th anniversary of The Biotech
Meeting of CEOs at Laguna Niguel, California, a conference sponsored
by Burrill & Co. and Kleiner Perkins Caufield & Byers. The CEOs voted
on what awards to present to their peers for corporate and individual
achievements.
During the third quarter, Pfizer presented new Exubera data of
particular importance for the healthcare professionals who treat
diabetes. At the 42nd European Association for the Study of Diabetes
in Copenhagen Denmark, held on September 14, 2006, Pfizer announced
data that adult patients with diabetes who took Exubera were able to
safely maintain good blood sugar control even if they developed a
respiratory infection or were exposed to passive (second-hand)
cigarette smoke. In addition, Pfizer announced that an analysis of a
previously reported study showed that Exubera has the potential to
encourage twice as many people with uncontrolled type 2 diabetes to
try insulin in countries where insulin is commonly delivered with a
pen (44 percent choosing insulin with Exubera availability versus 17
percent choosing insulin without Exubera availability). Finally,
Pfizer also announced that an analysis of five clinical trials showed
that people with either type 1 or type 2 diabetes who used Exubera
gained less weight than those using injectable insulin.
Exubera is marketed by Pfizer and is a product of a developmental
collaboration between Pfizer and Nektar. Exubera is currently
available in the U.S., U.K., Ireland, and Germany. It has been
approved in the European Union, U.S., Brazil and Mexico.
Under the agreement between the two companies, Nektar receives
royalties on Exubera sales as well as revenue for the manufacture of
the insulin powder and the Exubera Inhalers.
Nektar Proprietary Products: Key to Sustainable Growth and
Shareholder Value
"Our proprietary pipeline is the key to sustainable growth and
shareholder value," said Chess. "Our pulmonary and PEGylation
technologies are proven product engines to develop successful partner
products, and we intend to use them to continue to develop outstanding
products."
On September 18, 2006, Nektar announced that its Amphotericin B
Inhalation Powder (ABIP) product was granted orphan medicinal product
designation by the European Commission for the prevention of pulmonary
fungal infections in patients deemed at risk. In the U.S., the Food
and Drug Administration (FDA) granted both Fast Track designation and
Orphan Drug designation to ABIP for prevention of pulmonary fungal
infections in patients at risk for aspergillosis due to
immunosuppressive therapy. ABIP recently completed a multi-dose, dose
escalation clinical study in preparation for pivotal trials.
In October, Nektar had an encouraging clinical end-of-Phase-2
meeting with the FDA regarding its Amphotericin B Inhalation Powder
(ABIP) program. The FDA concurred with Nektar's plan to advance to
pivotal trials in 2007 and did not request additional clinical or
preclinical studies before proceeding.
Partner Products
Nektar and its partner, Zelos Therapeutics, a private
biopharmaceutical company focused on developing novel therapies for
patients suffering from osteoporosis, announced on September 21, 2006
the initiation of a Phase 1 clinical trial of an inhaled powder
formulation of Zelos' proprietary parathyroid hormone Ostabolin-C(TM)
(cyclic PTH (1-31)). Nektar and Zelos entered into a collaboration to
develop an inhaleable powder form of Ostabolin-C in January 2005.
Important Safety Information about Exubera
Patients should not take Exubera if they have poorly controlled or
unstable lung disease, or if they smoke or have stopped smoking less
than six months prior to starting Exubera treatment. If a patient
starts smoking or resumes smoking, he or she must stop using Exubera
and see a healthcare provider about a different treatment.
In clinical trials, mean treatment group differences between
Exubera and comparators showed that Exubera was associated with small,
non-progressive declines in lung function relative to comparator
treatments.
Before starting treatment with Exubera, a healthcare professional
will carry out a simple test to check lung function. This will help to
find out if Exubera is the right treatment for individual patients.
Once a patient starts treatment, it is recommended that a healthcare
provider check lung function again at six months and yearly
thereafter.
Like all medicines, Exubera can cause side effects. As with all
forms of insulin, a possible side effect of Exubera is low blood sugar
levels.
Some patients have reported a mild cough while taking Exubera,
which tended to occur within seconds to minutes after Exubera
inhalation. Coughing occurred less frequently as patients continued to
use Exubera.
Conference Call Information
Robert Chess, Nektar chairman and acting CEO, will host a
conference call for analysts and investors today beginning at 2:00
p.m. Pacific time to discuss further the company's performance.
Investors can access a live audio-only webcast through a link that
is posted on the Investor Relations section of Nektar's website at
http://www.nektar.com. The web broadcast of the conference call will
be available for replay through November 16, 2006.
Analysts and investors can also access the conference call live
via telephone by dialing (800) 640-9765 (U.S.); (847) 413-4837
(international). The passcode is 16034200 and the host is Robert
Chess. An audio replay will be available shortly following the call
through November 16, 2006 and can be accessed by dialing (877)
213-9653 (U.S.); or (630) 652-3041 (international) with a passcode of
16034200. In the event that any non-GAAP financial measure is
discussed on the conference call that is not described in the press
release, related information will be made available on the Investor
Relations page at the Nektar website as soon as practical after the
conclusion of the conference call.
About Nektar
Nektar Therapeutics is a biopharmaceutical company that develops
and enables differentiated therapeutics with its industry-leading
pulmonary and PEGylation technologies, expertise and manufacturing
capabilities. Nektar technology and know-how have enabled nine
approved products for partners, which include the world's leading
pharmaceutical and biotechnology companies. Nektar also develops its
own products by applying its technologies and expertise to existing
medicines to enhance performance, such as improving efficacy, safety
and compliance.
Non-GAAP Financial Measures
The company provides all information required in accordance with
GAAP, but it believes that evaluating its ongoing results of
operations may be difficult to understand if limited to reviewing only
GAAP financial results. In managing the company's business, management
reviews non-GAAP net loss and non-GAAP basic and diluted net loss per
common share which excludes, as applicable, SFAS 123R stock-based
compensation charges, litigation charges, and severance and
restructuring charges to evaluate the company's ongoing and future
financial and operating results.
Management does not itself, nor does it suggest that investors
should, consider such non-GAAP financial measures in isolation from,
or as a substitute for, GAAP financial measures. The company considers
and presents such non-GAAP financial measures in measuring, reporting,
and forecasting its financial results to provide management and
investors with an additional tool to evaluate the company's operating
results in a manner that focuses on what management believes to be the
company's ongoing business operations. Management believes that the
inclusion of non-GAAP financial measures provides consistency and
comparability with past reports of financial results and future
projections of revenue and net loss financial measures. Investors
should note, however, that the non-GAAP financial measures used by the
company may not be the same non-GAAP financial measures as, and may
not be calculated in the same manner as that of other companies with
which investors may compare the financial results of the company.
Management believes it is useful for the company and investors to
review both GAAP information that includes the expenses and charges
mentioned above and the non-GAAP financial measures that exclude such
special expenses and charges to have a better understanding of the
overall performance of the company's business, its allocation of
resources and its ability to perform in the future. Investors are
encouraged to review the related GAAP financial measures and the
reconciliation of these non-GAAP financial measures to their most
directly comparable GAAP financial measure.
This press release contains forward-looking statements that
reflect management's current views and expectations as to the Exubera
product commercial roll-out and market prospects, Exubera
manufacturing levels, clinical plans and expectations for the clinical
advancement of proprietary and partner products, prospects for the
business and financial objectives, and financial estimates for the
2006 and 2007 calendar years. These forward-looking statements involve
uncertainties and other risks, including but not limited to: (i) the
success of the Exubera commercial launch (ii) the company's and
Pfizer's ability to manufacture and supply sufficient quantities of
Exubera product to meet patient demand (iii) the discovery of any new
or more severe side effects or negative efficacy findings for Exubera
or any product liability claims related thereto (iv) investment in
proprietary products prior to seeking partner collaborations may
adversely impact results of operations and financial condition (v)
Nektar success or the success of Nektar's partners in obtaining
regulatory approvals (vi) a material negative impact on results of
operations for future periods as a result of the application of SFAS
123R related to expensing of stock-based compensation, and (vii)
additional charges and expenses that may be incurred as we restructure
the company in order to focus on our core assets. Other important
risks and uncertainties are detailed in the company's reports and
other filings with the SEC, including its most recent Annual Report on
Form 10-K, Quarterly Report on Form 10-Q, and Current Reports on Form
8-K. Actual results could differ materially from the forward-looking
statements contained in this press release. The company undertakes no
obligation to update forward-looking statements, whether as a result
of new information, future events or otherwise.
Exubera is a registered trademark of Pfizer Inc.
NEKTAR THERAPEUTICS
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
( In thousands, except per share information)
Unaudited Unaudited
------------------- --------------------
Three-Months Ended Nine-Months Ended
September 30, September 30,
------------------- --------------------
2006 2005 2006 2005
--------- --------- ---------- ---------
Revenue:
Contract research
revenue $15,111 $23,657 $44,250 $62,737
Product sales and
royalty revenue 41,451 8,450 98,005 20,313
Exubera(R)
commercialization
readiness revenue 2,070 4,247 5,559 10,348
--------- -------------------- ---------
Total revenue 58,632 36,354 147,814 93,398
Operating costs and expenses:
Cost of goods sold 30,137 6,125 73,821 16,813
Exubera(R)
commercialization
readiness costs 1,042 3,075 3,126 8,035
Research and
development 34,985 38,591 108,016 109,321
General and
administrative 14,442 10,948 60,878 30,193
Litigation settlement - - 17,710 -
Amortization of other
intangible assets 708 982 3,331 2,945
--------- --------- ---------- ---------
Total operating costs and
expenses 81,314 59,721 266,882 167,307
--------- --------- ---------- ---------
Loss from operations (22,682) (23,367) (119,068) (73,909)
Loss on extinguishment of debt - (303) - (303)
Other income (expense), net 2,273 (32) 1,181 (1,435)
Interest income 6,060 2,899 17,316 7,683
Interest expense (5,255) (2,992) (15,335) (8,908)
--------- --------- ---------- ---------
Loss before provision for
income taxes (19,604) (23,795) (115,906) (76,872)
Benefit (provision) for income
taxes - - - -
--------- --------- ---------- ---------
Net loss $(19,604) $(23,795) $(115,906) $(76,872)
========= ========= ========== =========
Basic and diluted net loss per
common share $(0.22) $(0.28) $(1.29) $(0.90)
Shares used in computing basic
and diluted net loss per
share 90,017 86,228 89,550 85,331
NEKTAR THERAPEUTICS
Reconciliation of GAAP Financial Measures to Non-GAAP Financial
Measures
( In thousands, except per share information)
Unaudited Unaudited
------------------- --------------------
Three-Months Ended Nine-Months Ended
September 30, September 30,
------------------- --------------------
2006 2005 2006 2005
--------- --------- ---------- ---------
GAAP net loss $(19,604) $(23,795) $(115,906) $(76,872)
Adjustments to GAAP net loss:
SFAS 123R stock-based
compensation expense,
excluding severance 2,918 - 13,305 -
Litigation settlement - - 17,710 -
Severance and restructuring
charges 2,712 - 21,595 -
--------- --------- ---------- ---------
Non-GAAP net loss (1) $(13,974) $(23,795) $(63,296) $(76,872)
========================================
GAAP basic and diluted net
loss per common share $(0.22) $(0.28) $(1.29) $(0.90)
Adjustments to GAAP basic and diluted
net loss per common share:
SFAS 123R stock-based
compensation expense,
excluding severance $0.03 $- $0.15 $-
Litigation settlement $- $- $0.20 $-
Severance and restructuring
charges $0.03 $- $0.24 $-
--------- --------- ---------- ---------
Non-GAAP basic and diluted net
loss per common share (1) $(0.16) $(0.28) $(0.71) $(0.90)
========= ========= ========== =========
Shares used in computing non-
GAAP basic and diluted net
loss per share 90,017 86,228 89,550 85,331
(1) These non-GAAP financial measures are not presented as a measure
of operating results and should not be construed as an alternative to
either (i) income from operations or (ii) cash flows from operating
activities. The company's management provides these non-GAAP
financial measures to present investors with additional information
that the company's management considers in assessing the company's
results of operations, and to enhance investors' overall
understanding of the company's financial performance.
NEKTAR THERAPEUTICS
CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands)
September 30, December 31,
2006 2005
(unaudited) (a)
------------- ------------
ASSETS
Current assets:
Cash, cash equivalents and short-
term investments $481,608 $476,201
Inventory 15,795 18,627
Other current assets 49,029 25,015
------------- ------------
Total current assets 546,432 519,843
Investments in marketable securities 9,342 90,222
Property and equipment, net 136,580 142,127
Goodwill 78,431 78,431
Other intangible assets, net 9,831 13,452
Other assets 9,404 14,479
------------- ------------
$790,020 $858,554
============= ============
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable and accrued
liabilities $40,633 $53,626
Capital lease obligations - current 604 482
Convertible subordinated notes and
debentures - current 36,026 -
Deferred revenue - current 18,066 15,487
------------- ------------
Total current liabilities 95,329 69,595
Convertible subordinated notes and
debentures 381,627 417,653
Accrued rent 2,295 2,409
Capital lease obligations 19,814 20,276
Deferred revenue 23,278 8,374
Other long-term liabilities 15,994 13,436
Stockholders' equity:
Preferred stock at par - -
Common stock at par 9 9
Capital in excess of par 1,269,341 1,233,690
Deferred compensation - (2,949)
Accumulated other comprehensive
loss 471 (1,707)
Accumulated deficit (1,018,138) (902,232)
------------- ------------
Total stockholders' equity 251,683 326,811
------------- ------------
$790,020 $858,554
============= ============
(a) The balance sheet at December 31, 2005 has been derived from the
audited financial statements at that date but does not include all of
the information and footnotes required by accounting principles
generally accepted in the United States for complete financial
statements.
Supplemental Table
NEKTAR THERAPEUTICS
Reconciliation of Non-GAAP Projected Financial Guidance for 2006
Refer to the discussion of non-GAAP financial measures included in the
accompanying press release for additional information.
2006 Projected
Financial Guidance
---------------------
2006 Exubera-related projected revenue range $90 to $100
2006 other revenue 100 110
--------- -------
2006 projected total revenue range $190 to $210
========= =======
Projected GAAP net loss $(155) to $(170)
Adjustments to GAAP net loss:
SFAS 123R stock-based compensation expense,
excluding severance related charges 22 22
Litigation charges 18 18
Severance and restructuring charges 20 20
--------- -------
Projected Non-GAAP net loss $(95) to $(110)
========= =======
Supplemental Table
NEKTAR THERAPEUTICS
Reconciliation of Non-GAAP Projected Financial Guidance for 2007
(In millions)
Refer to the discussion of non-GAAP financial measures included in the
accompanying press release for additional information.
2007 Projected
Financial
Guidance
-----------------
2007 Exubera-related projected revenue range $110 to $130
2007 other revenue 100 120
------ ------
2007 projected total revenue range $210 to $250
====== ======
Projected GAAP net loss $(110) to $(130)
Adjustments to GAAP net loss:
SFAS 123R stock-based compensation expense,
excluding severance related charges 35 35
Projected Non-GAAP net loss $(75) to $(95)
====== ======
CONTACT: Nektar Therapeutics
Joyce Strand, 650-631-3138
Jennifer Ruddock, 650-631-4954