Revance Releases Third Quarter 2017 Results
-SAKURA 1 & 2 Phase 3 pivotal trials on track to report topline results before year-end 2017-
-SAKURA 3 open-label safety study for glabellar lines has completed enrollment of more than 2,100 subjects-
Revance Therapeutics, Inc. (NASDAQ:RVNC), a biotechnology company developing botulinum toxin products for use in treating
aesthetic and therapeutic conditions, today announced results for the third quarter ended September 30, 2017.
Recent Highlights and Upcoming Milestones for DaxibotulinumtoxinA for Injection (RT002)
- Completed enrollment of more than 2,100 subjects at multiple sites in the United States and Canada
for SAKURA open-label safety Phase 3 study of RT002 injectable for the treatment of glabellar (frown) lines; Revance expects to
complete the study in the second half of 2018.
- SAKURA 1 & 2 Phase 3 pivotal trials remain on track to report topline results before the end
of 2017.
- Completed enrollment of the Phase 2 trial of RT002 injectable in the management of plantar fasciitis
in October of 2017. Revance remains on track to report topline 8-week safety and efficacy results at year-end.
- Scheduled meeting for the fourth quarter of 2017 with the U.S. Food & Drug Administration to
review the data from the Phase 2 trial of RT002 for the treatment of moderate to severe isolated cervical dystonia and to
determine next steps for the program.
- Announced the appointment of Mark Foley, an industry veteran with more than 25 years of operational
and investment experience in the healthcare arena, to Revance’s Board of Directors and Todd Zavodnick, a 20-year industry leader,
joining our executive team as Chief Commercial Officer and President, Aesthetics & Therapeutics.
“We’ve made excellent progress in 2017 and now expect to report topline results for both our SAKURA Phase 3 pivotal trials for
glabellar lines and Phase 2 trial for plantar fasciitis before year-end,” said Dan Browne, President and Chief Executive Officer at
Revance. “We believe RT002 will set a new standard of performance for neuromodulators and give patients and physicians a profoundly
different experience in both aesthetic and therapeutic indications. There is growing interest in RT002 within the medical
communities, as the concept of a neuromodulator with improved outcomes and durability has been resonating well with physicians at
conferences throughout the year. By year end, we will have validated the potential advantages of RT002 injectable not just in
wrinkle reduction, but in two key therapeutic areas where better patient outcomes are highly valued.”
Summary Financial Results
Cash and investments as of September 30, 2017 were $153.4 million.
Research and development expenses for the three and nine months ended September 30, 2017 were $21.6 million and $59.4
million compared to $10.3 million and $37.9 million for the same periods in 2016, respectively. The change in research and
development expenses is primarily due to increased clinical trial activity for RT002 injectable, including the SAKURA Phase 3
program, the plantar fasciitis Phase 2 trial, and the cervical dystonia Phase 2 trial, along with increased pre-commercial
manufacturing activities.
General and administrative expenses for the three and nine months ended September 30, 2017 were $9.1 million and $25.5
million compared to $7.5 million and $22.0 million for the same periods in 2016, respectively. The increase in general and
administrative expenses is primarily due to increased personnel, pre-commercial, and information technology expenses.
Total operating expenses for the three and nine months ended September 30, 2017 were $30.8 million and $84.9 million
compared to $17.8 million and $61.8 million for the same periods in 2016, respectively. Stock-based compensation for the three and
nine months ended September 30, 2017 was $3.1 million and $9.8 million, respectively. When excluding depreciation and stock-based
compensation, total operating expenses for the three and nine months ended September 30, 2017 were $27.3 million and $74.0 million,
respectively.
Net loss for the three and nine months ended September 30, 2017 was $30.7 million and $84.7 million compared to $18.0
million and $62.5 million for the same periods in 2016, respectively.
2017 Financial Outlook
Revance reaffirmed its financial guidance provided in January 2017. Revance expects cash burn for 2017 to be in the range
of $102 to $112 million. Revance expects 2017 GAAP operating expense to be in the range
of $108 to $119 million, which when excluding depreciation of $1 to $2 million and estimated
stock-based compensation of $13 to $15 million, results in projected 2017 non-GAAP operating expense
of $94 to $102 million. Revance anticipates 2017 GAAP research and development expense to be in the range
of $75 to $83 million, which when excluding depreciation of $1 to $2 million and estimated
stock-based compensation of $5 to $6 million, results in projected 2017 non-GAAP research and development expense
of $69 to $75 million.
Conference Call
Individuals interested in listening to the conference call today, November 2, at 1:30pm PT/4:30pm ET, may do so by dialing (855)
453-3827 for domestic callers, or (484) 756-4301 for international callers and reference conference ID: 99298055; or from the
webcast link in the investor relations section of the Company's website at: http://investors.revance.com/index.cfm.
A replay of the call will be available beginning today at 4:30pm PT/7:30pm ET through 4:30pm PT/7:30pm ET on November 3, 2017.
To access the replay, dial (855) 859-2056 or (404) 537-3406 and reference conference ID: 99298055. The webcast will be available in
the investor relations section on the Company's website for 30 days following the completion of the call.
About Revance Therapeutics, Inc.
Revance, a Silicon Valley-based biotechnology company, is committed to the advancement of remarkable science. The company
is developing a portfolio of products for aesthetic medicine and underserved therapeutic specialties, including dermatology,
orthopedics and neurology. Revance’s science is based upon a proprietary peptide technology, which when combined with active drug
molecules, may help address current unmet needs. Revance’s initial focus is on developing daxibotulinumtoxinA, the company’s highly
purified botulinum toxin, for a broad spectrum of aesthetic and therapeutic indications, including facial wrinkles and muscle
movement disorders.
The company’s lead drug candidate, DaxibotulinumtoxinA for Injection (RT002), is currently in development for the treatment of
glabellar lines, cervical dystonia and plantar fasciitis with the potential to be the first long-acting neuromodulator. The company
holds worldwide rights to RT002 injectable and RT001 topical and the pharmaceutical uses of its proprietary peptide technology
platform. More information on Revance may be found at www.revance.com.
“Revance Therapeutics” and the Revance logo are registered trademarks of Revance Therapeutics, Inc.
Forward-Looking Statements
This press release contains forward-looking statements, including statements related to Revance Therapeutics' 2017 Financial
Outlook and other financial performance, the process and timing of, and ability to complete, current and anticipated future
clinical development of our investigational drug product candidates, including but not limited to initiation and design of clinical
studies for current and future indications, related results and reporting of such results; statements about our business strategy,
timeline and other goals and market for our anticipated products, plans and prospects; and statements about our ability to obtain
regulatory approval; and potential benefits of our drug product candidates and our technologies.
Forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially from
our expectations. These risks and uncertainties include, but are not limited to: the outcome, cost, and timing of our product
development activities and clinical trials; the uncertain clinical development process, including the risk that clinical trials may
not have an effective design or generate positive results; our ability to obtain and maintain regulatory approval of our drug
product candidates; our ability to obtain funding for our operations; our plans to research, develop, and commercialize our drug
product candidates; our ability to achieve market acceptance of our drug product candidates; unanticipated costs or delays in
research, development, and commercialization efforts; the applicability of clinical study results to actual outcomes; the size and
growth potential of the markets for our drug product candidates; our ability to successfully commercialize our drug product
candidates and the timing of commercialization activities; the rate and degree of market acceptance of our drug product candidates;
our ability to develop sales and marketing capabilities; the accuracy of our estimates regarding expenses, future revenues, capital
requirements and needs for financing; our ability to continue obtaining and maintaining intellectual property protection for our
drug product candidates; and other risks. Detailed information regarding factors that may cause actual results to differ materially
from the results expressed or implied by statements in this press release may be found in Revance's periodic filings with
the Securities and Exchange Commission (the "SEC"), including factors described in the section entitled "Risk Factors" of
our quarterly report on Form 10-Q filed August 4, 2017. These forward-looking statements speak only as of the date hereof.
Revance disclaims any obligation to update these forward-looking statements.
Use of Non-GAAP Financial Measures
Revance has presented certain non-GAAP financial measures in this release. This release and the reconciliation tables included
herein include total non-GAAP operating expense and non-GAAP R&D expense, both of which exclude depreciation and stock-based
compensation. Revance excludes depreciation costs and stock-based compensation expense because management believes the exclusion of
these items is helpful to investors to evaluate Revance's recurring operational performance. Revance management uses these non-GAAP
financial measures to monitor and evaluate its operating results and trends on an on-going basis, and internally for operating,
budgeting and financial planning purposes. The non-GAAP financial measures should be considered in addition to results prepared in
accordance with GAAP, but should not be considered a substitute for or superior to GAAP results.
REVANCE THERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(In thousands, except share and per share amounts)
(Unaudited)
|
|
|
|
|
|
|
|
September 30, |
|
December 31, |
|
|
2017 |
|
2016 |
ASSETS |
CURRENT ASSETS |
|
|
|
|
Cash and cash equivalents |
|
$ |
56,323 |
|
|
$ |
63,502 |
|
Short-term investments |
|
97,117 |
|
|
122,026 |
|
Prepaid expenses and other current assets |
|
2,827 |
|
|
7,167 |
|
Total current assets |
|
156,267 |
|
|
192,695 |
|
Property and equipment, net |
|
11,500 |
|
|
10,585 |
|
Restricted cash |
|
580 |
|
|
580 |
|
Other non-current assets |
|
836 |
|
|
500 |
|
TOTAL ASSETS |
|
$ |
169,183 |
|
|
$ |
204,360 |
|
LIABILITIES AND STOCKHOLDERS’ EQUITY |
CURRENT LIABILITIES |
|
|
|
|
Accounts payable |
|
$ |
6,680 |
|
|
$ |
3,754 |
|
Accruals and other current liabilities |
|
12,069 |
|
|
12,418 |
|
Financing obligations, current portion |
|
2,727 |
|
|
3,475 |
|
Total current liabilities |
|
21,476 |
|
|
19,647 |
|
Financing obligations, net of current portion |
|
— |
|
|
1,872 |
|
Derivative liability associated with Medicis settlement |
|
2,233 |
|
|
2,022 |
|
Deferred rent |
|
3,418 |
|
|
3,648 |
|
Other non-current liabilities |
|
— |
|
|
100 |
|
TOTAL LIABILITIES |
|
27,127 |
|
|
27,289 |
|
Commitments and Contingencies |
|
|
|
|
STOCKHOLDERS’ EQUITY |
|
|
|
|
Common stock, par value $0.001 per share — 95,000,000 shares authorized as of
September 30, 2017 and December 31, 2016; 30,935,094 and 28,648,954 shares
issued and outstanding as of September 30, 2017 and December 31, 2016,
respectively
|
|
31 |
|
|
29 |
|
Additional paid-in capital |
|
648,329 |
|
|
598,630 |
|
Accumulated other comprehensive loss |
|
(43 |
) |
|
(45 |
) |
Accumulated deficit |
|
(506,261 |
) |
|
(421,543 |
) |
TOTAL STOCKHOLDERS’ EQUITY |
|
142,056 |
|
|
177,071 |
|
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY |
|
$ |
169,183 |
|
|
$ |
204,360 |
|
REVANCE THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share amounts)
(Unaudited)
|
|
|
|
|
|
|
|
Three Months Ended
September 30, |
|
Nine Months Ended
September 30, |
|
|
2017 |
|
2016 |
|
2017 |
|
2016 |
Revenue |
|
$ |
75 |
|
|
$ |
75 |
|
|
$ |
225 |
|
|
$ |
225 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
Research and development |
|
21,643 |
|
|
10,296 |
|
|
59,357 |
|
|
37,851 |
|
General and administrative |
|
9,148 |
|
|
7,502 |
|
|
25,511 |
|
|
21,975 |
|
Loss on impairment |
|
— |
|
|
— |
|
|
— |
|
|
1,949 |
|
Total operating expenses |
|
30,791 |
|
|
17,798 |
|
|
84,868 |
|
|
61,775 |
|
Loss from operations |
|
(30,716 |
) |
|
(17,723 |
) |
|
(84,643 |
) |
|
(61,550 |
) |
Interest income |
|
341 |
|
|
306 |
|
|
999 |
|
|
940 |
|
Interest expense |
|
(104 |
) |
|
(256 |
) |
|
(439 |
) |
|
(857 |
) |
Change in fair value of derivative liability associated with Medicis
settlement
|
|
(44 |
) |
|
(167 |
) |
|
(211 |
) |
|
(595 |
) |
Other expense, net |
|
(128 |
) |
|
(138 |
) |
|
(386 |
) |
|
(406 |
) |
Net loss |
|
(30,651 |
) |
|
(17,978 |
) |
|
(84,680 |
) |
|
(62,468 |
) |
Unrealized gain (loss) on available for sale securities |
|
72 |
|
|
(132 |
) |
|
3 |
|
|
56 |
|
Comprehensive loss |
|
$ |
(30,579 |
) |
|
$ |
(18,110 |
) |
|
$ |
(84,677 |
) |
|
$ |
(62,412 |
) |
Net loss attributable to common stockholders: |
|
|
|
|
|
|
|
|
Basic and Diluted |
|
$ |
(30,651 |
) |
|
$ |
(17,978 |
) |
|
$ |
(84,680 |
) |
|
$ |
(62,468 |
) |
Net loss per share attributable to common stockholders: |
|
|
|
|
|
|
|
|
Basic and Diluted |
|
$ |
(1.01 |
) |
|
$ |
(0.64 |
) |
|
$ |
(2.86 |
) |
|
$ |
(2.22 |
) |
Weighted-average number of shares used in computing net loss per
share attributable to common stockholders:
|
|
|
|
|
|
|
|
|
Basic and Diluted |
|
30,270,260 |
|
|
28,160,458 |
|
|
29,623,805 |
|
|
28,085,541 |
|
Revance Therapeutics, Inc.
2017 Financial Results
(Unaudited)
|
|
Reconciliation of GAAP Operating Expense to Non-GAAP Operating Expense
(In thousands)
|
|
|
|
|
|
|
|
Three Months Ended |
|
Nine Months Ended |
|
|
September 30, 2017 |
|
September 30, 2017 |
Operating expense: |
|
|
|
|
GAAP operating expense |
|
$ |
30,791 |
|
|
$ |
84,868 |
|
Adjustments: |
|
|
|
|
Stock-based compensation |
|
(3,146 |
) |
|
(9,820 |
) |
Depreciation |
|
(375 |
) |
|
(1,096 |
) |
Non-GAAP operating expense |
|
$ |
27,270 |
|
|
$ |
73,952 |
|
Revance Therapeutics, Inc.
2017 Financial Guidance
|
|
Reconciliation of GAAP Operating Expense to Non-GAAP Operating Expense
(In thousands)
|
|
|
|
|
|
Fiscal Year |
|
|
2017 |
|
|
Low |
|
High |
Operating expense: |
|
|
|
|
|
|
GAAP operating expense |
|
$ |
108,000 |
|
|
$ |
119,000 |
|
Adjustments: |
|
|
|
|
|
|
Stock-based compensation |
|
|
(13,000 |
) |
|
|
(15,000 |
) |
Depreciation |
|
|
(1,000 |
) |
|
|
(2,000 |
) |
Non-GAAP operating expense |
|
$ |
94,000 |
|
|
$ |
102,000 |
|
|
|
|
|
|
|
|
Reconciliation of GAAP R&D Expense to Non-GAAP R&D Expense
(In thousands)
|
|
|
|
|
|
|
|
|
|
Fiscal Year |
|
|
2017 |
|
|
Low |
|
High |
R&D expense: |
|
|
|
|
|
|
GAAP R&D expense |
|
$ |
75,000 |
|
|
$ |
83,000 |
|
Adjustments: |
|
|
|
|
|
|
Stock-based compensation |
|
|
(5,000 |
) |
|
|
(6,000 |
) |
Depreciation |
|
|
(1,000 |
) |
|
|
(2,000 |
) |
Non-GAAP R&D expense |
|
$ |
69,000 |
|
|
$ |
75,000 |
|
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Investors:
Revance Therapeutics, Inc.:
Jeanie Herbert, 714-325-3584
jherbert@revance.com
or
Burns McClellan, Inc.:
Ami Bavishi, 212-213-0006
abavishi@burnsmc.com
or
Trade Media, Inc.:
Nadine Tosk, 504-453-8344
nadinepr@gmail.com
View source version on businesswire.com: http://www.businesswire.com/news/home/20171102006485/en/