FOAMIX PHARMACEUTICALS LTD. REHOVOT, Israel, May 9, 2017 /PRNewswire/ -- Foamix Pharmaceuticals Ltd. (NASDAQ: FOMX) ("Foamix Pharmaceuticals" or the "Company"), a clinical stage specialty pharmaceutical company focused on developing and commercializing proprietary topical foams to address unmet needs in dermatology, announced today financial results for the three months ended March 31, 2017.
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Clinical, business and corporate developments for the three months ended March 31, 2017 and to date:
-- On March 27, 2017, we provided the top-line data from our two Phase 3
clinical trials (Trial 04 and 05) for FMX101 in the treatment of
moderate-to-severe acne. In the intent-to-treat analysis, FMX101
demonstrated statistical significance compared to vehicle on both
co-primary endpoints in Trial 05 (specifically the absolute reduction in
inflammatory lesions at week 12, and investigator global assessment
(IGA) treatment success at week 12 compared to baseline). In Trial 04,
statistical significance was demonstrated for FMX101 compared to vehicle
in the co-primary endpoint of absolute reduction in inflammatory
lesions, however, statistical significance was not achieved in the
co-primary endpoint of IGA treatment success.
-- On May 3, 2017, we provided new data from our two Phase 3 clinical
trials for FMX101, including pooled analysis of our co-primary endpoints
and certain secondary clinical endpoints (absolute reduction of
non-inflammatory lesions at week 12; and percent change in inflammatory
lesions at weeks 3, 6, 9 and 12). Highlights from our further analyses
included:
-- Statistical significance was demonstrated for FMX101 compared to
vehicle in the pooled analysis of both co-primary endpoints -
absolute reduction of inflammatory lesions and Investigator's Global
Assessment (IGA)
-- % Change in inflammatory lesion count was statistically significant
in both Trials 04 and 05 at all timepoints (beginning at Week 3)
-- Non-inflammatory lesion count reduction at Week 12 was statistically
significant in both Trials 04 and 05
-- Overall high level of patient satisfaction with FMX101 (based on
patient satisfaction questionnaires).
-- FMX101 was generally safe and tolerable. No serious adverse events
drug-related systemic side effects were recorded.
-- Further to sharing the detailed analyses, we announced that based on the
results of the first two pivotal trials (Trial 04 and 05), we intend to
conduct a third U.S. Phase 3 trial in patients with moderate-to-severe
acne. This double-blind, vehicle-controlled trial is planned to enroll
1,500 patients who will be randomized 1:1 (FMX101 vs vehicle) across an
estimated 80 investigator sites. The trial is expected to commence
mid-year. If the results are positive, this trial will form the basis
for a New Drug Application (NDA) which the company plans to submit in
the second half of 2018.
-- The two Phase 3 clinical trials for FMX103 in patients with
moderate-to-severe papulopustular rosacea are expected to commence
mid-2017. We also announced on May 3, 2017, that we plan to increase the
sample size for each of the two Phase 3 trials from 600 to 750 patients
(total of 1,500 patients) randomized 2:1 (FMX103 vs vehicle) across an
estimated 80 investigator sites in the U.S. FMX103 demonstrated
clinically and statistically significant efficacy in treating
moderate-to-severe rosacea in a Phase 2 trial which enrolled 233
patients across 18 sites in Germany.
-- During the first quarter of 2017 we successfully manufactured three
registration-quality batches for FMX101.
-- U.S. Sales of Finacea(®) Foam, azelaic acid 15% for the treatment of
rosacea, continue to grow.
-- Based on sales of Finacea(®) Foam reported by Bayer HealthCare AG
for Q1, 2017 Foamix is entitled to royalty payments of $927,000, up
26% from the fourth quarter of 2016.
-- Finacea(®) Foam was developed through a research and development
collaboration between Foamix and Bayer, utilizing Foamix's
proprietary foam technology platform. The drug was launched by Bayer
in the USA in September 2015.
Financial highlights for the three months ended March 31, 2017:
-- Total revenues were $927,000 compared with $745,000 for the three months
ended March 31, 2016. The increase is due to increase in sales of
Finacea(®) Foam by Bayer HealthCare AG.
-- Research and development expenses were $12.7 million, compared with $3.6
million in the three months ended March 31, 2016. This increase resulted
primarily from an increase in costs relating to the FMX101 and FMX103
clinical trials as well as an increase in payroll and related expenses
due to an increase in the number of R&D employees.
-- Selling, general and administrative expenses were $2.8 million, compared
with $1.7 million in the three months ended March 31, 2016. The
increase in selling, general and administrative expenses resulted
primarily from increases in payroll and other payroll-related expenses,
market research costs, advisors, maintenance and office expenses.
-- Operating expenses totaled $15.5 million, compared with $5.3 million in
the three months ended March 31, 2016.
-- Net loss was $14.4 million or $0.39 per share, basic and diluted,
compared with a loss of $4.5 million or $0.15 per share, basic and
diluted, for the three months ended March 31, 2016.
-- Cash and investments as of March 31, 2017 totaled $118.7 million,
compared with $131.0 million as of December 31, 2016.
Management overview
-- On March 27, 2017, we provided the top-line data from our two Phase 3
clinical trials (Trial 04 and 05) for FMX101 in the treatment of
moderate-to-severe acne. In the intent-to-treat analysis, FMX101
demonstrated statistical significance compared to vehicle on both
co-primary endpoints in Trial 05 (specifically the absolute reduction in
inflammatory lesions at week 12, and investigator global assessment
(IGA) treatment success at week 12 compared to baseline). In Trial 04,
statistical significance was demonstrated for FMX101 compared to vehicle
in the co-primary endpoint of absolute reduction in inflammatory
lesions, however, statistical significance was not achieved in the
co-primary endpoint of IGA treatment success. On May 3, 2017, we
provided new data from our two Phase 3 clinical trials for FMX101,
including pooled analysis of our co-primary endpoints and certain
secondary clinical endpoints (absolute reduction of non-inflammatory
lesions at week 12; and percent change in inflammatory lesions at weeks
3, 6, 9 and 12). Statistical significance was demonstrated for FMX101
compared to vehicle in the pooled analysis of the co-primary endpoints
as well as the secondary endpoints presented.
Co-primary endpoint - Absolute change from baseline in inflammatory lesion count at week 12:
-- Trial 04: reduction of 14.16 lesions (or -14.16) for FMX101 and
reduction of 11.17 lesions (or -11.17) for the vehicle (p<0.01)
-- Trial 05: -13.46 for FMX101 and -10.72 for vehicle (p<0.01)
-- Pooled Analysis: Absolute change in inflammatory lesion count was -13.79
for the FMX101, 4% treatment group and -10.94 for vehicle (p=0.0001)
Co-primary endpoint - Proportion of patients with Investigator's Global Assessment (IGA) success at week 12:
-- Trial 04: IGA treatment success for FMX101, 4% treatment group was
8.09% versus 4.77% in vehicle (p=0.2178)
-- Trial 05: IGA treatment success for FMX101, 4% treatment group was
14.67% versus 7.89% in vehicle (p<0.05)
-- Pooled Analysis: IGA treatment success was 11.51% for FMX101, 4%
treatment group and 6.34% for vehicle (p<0.05)
Secondary efficacy endpoint - Percent change from baseline in inflammatory lesion count at weeks 3, 6, 9 and 12:
-- Trial 04: reduction of 29% for FMX101 vs. reduction of 19% for vehicle,
or -29% vs. -19%, at week 3 (p<.001); -37% vs. -26% at week 6 (p<.001);
-42% vs. -28% at week 9 (p<.0001); and -44% vs. -34% at week 12 (p<0.01)
-- Trial 05: reduction of 34% for FMX101 vs. reduction of 21% for vehicle,
or -34% vs. -21%, at week 3 (p<.0001); -39% vs. -27% at week 6
(p<.0001); -43% vs. -31% at week 9 (p<.001); and: -43% vs. -34% at week
12 (p<0.01)
Secondary efficacy endpoint - Absolute change from baseline in non-inflammatory lesion count at week 12:
-- Trial 04: reduction of 16.45 lesions (or -16.45) for the FMX101, 4%
treatment group and reduction of 10.30 lesions (or -10.30) for the
vehicle (p<0.01)
-- Trial 05: reduction of 13.20 (or -13.20) for the FMX101, 4% treatment
group and reduction of 7.00 (or -7.00) for the vehicle (p<0.05)
-- Pooled Analysis: Absolute change in non-inflammatory lesion count was
-14.76 for the FMX101, 4% treatment group and -8.64 for vehicle (p<0.01)
-- As we announced on May 3, 2017, based on the results of the first two
pivotal trials (Studies 04 and 05), the company intends to conduct a
third U.S. Phase 3 trial in patients with moderate-to-severe acne. If
the results are positive, this trial will form the basis for an NDA
which the company plans to submit in the second half of 2018. This
planned clinical trial will be conducted at approximately 80
investigator sites in the U.S. In order to achieve the necessary
statistical power compared with the prior Phase 3 trials, the target
patient enrollment number has been increased to 1,500. Patients will be
randomized 1:1 to receive either FMX101 (minocycline foam 4%) or vehicle
foam once daily over 12 weeks. The co-primary efficacy endpoints will be
identical to the prior Phase 3 trials: (1) mean change from baseline in
the inflammatory lesion count, and (2) proportion of patients with IGA
scores of "Clear" or "Almost Clear", with improvement of at least two
grades from baseline. The inclusion criteria will be consistent with the
prior Phase 3 trials.
-- We intend to meet with the FDA to review the results of our Phase 3
clinical trials for FMX101 (Trial 04 and 05) and our third Phase 3
trial, which we expect to commence mid-year.
-- Following the results of the first two pivotal trials for FMX101 in
moderate-to-severe acne, we have also reviewed our Phase 3 program for
FMX103 in papulopustular rosacea, which is expected to commence around
mid-2017. Based on the outcome of the Phase 3 studies for FMX101, and
the planned increase in the number of patients to be enrolled in the
third Phase 3 trial in acne, we also intend to increase the sample size
for the two planned Phase 3 studies for FMX103 in papulopustular
rosacea. The sample size will be increased from 600 patients per trial
to 750 patients per trial, for a total of 1,500 patients across the two
studies.
-- Regarding manufacturing, we have successfully completed the scale-up
process for FMX101 to a commercial batch size of one-ton. The production
of three registration batches has been completed.
-- In addition to our internal drug development pipeline, we have
development and license agreements relating to our proprietary foam
technology with other pharmaceutical companies, including Bayer
Healthcare and others, in various stages of development and
commercialization. Our agreements with these licensees entitle us to
development fees, contingent payments and royalties upon
commercialization.
-- In September 2015, Bayer Healthcare began selling Finacea(®) Foam
(azelaic acid 15% for the treatment of rosacea) in the U.S. Finacea(®)
foam is a prescription foam product which was developed as part of a
research and development collaboration between Foamix and Bayer,
utilizing Foamix's proprietary foam technology platform. According to
our license agreement with Bayer, we are entitled to royalties upon
commercialization of Finacea Foam. For the three months ended March 31,
2017, we were entitled to royalties from Bayer in an amount of $927,000,
up 26% from the fourth quarter of 2016.
-- The Company is currently well-capitalized and has sufficient cash to
fund our key development programs (FMX101 and FMX103) through NDA
registration.
Financial results for the three months ended March 31, 2017
Revenues
Total revenues for the three-month ended March 31, 2017 were $927,000 compared with $745,000 for the three months ended March 31, 2016. The increase is due to increase in sales of Finacea(®) Foam by Bayer HealthCare AG.
Operating Expenses
Our operating expenses for the three months ended March 31, 2017, and three months ended March 31, 2016, were as follows:
Research and Development Expenses
Research and development expenses increased by $9.1 million, or 255%, from $3.6 million in the three months ended March 31, 2016, to $12.7 million in the three months ended March 31, 2017. The increase in research and development expenses resulted primarily from an increase of $7.9 million in costs relating to the FMX101 and FMX103 clinical trials and an increase of $1.1 million in payroll and payroll related expenses (including bonuses and equity-based compensation) due to an increase in the number of R&D employees.
Selling, General and Administrative Expenses
Selling, general and administrative expenses increased by $1.1 million, or 65%, from $1.7 million in the three months ended March 31, 2016, to $2.8 million in the three months ended March 31, 2017. The increase in selling, general and administrative expenses resulted primarily from an increase of $300,000 in payroll and other payroll-related expenses (including bonuses and equity-based compensation), an increase of $250,000 in advisors, consultants and other professional services, $102,000 in market research costs and $122,000 in rent, maintenance and office expenses.
Finance Income, Net
For the three months ended March 31, 2017, we recorded financial income of $257,000 compared to financial income of $174,000 recorded for the three months ended March 31, 2016. The financial income for the three months ended March 31, 2017 and 2016 resulted mostly from interest and financial gains from our cash investments.
Net Loss
For the three months ended March 31, 2017, we recorded a loss of $14.4 million or $0.39 per share, basic and diluted, compared with a loss of $4.5 million or $0.15 per share, basic and diluted, for the three months ended March 31, 2016.
Liquidity and Capital Resources
As of March 31, 2017, we had cash and investments of $118.7 million, compared with $131.0 million as of December 31, 2016. The decrease was mostly due to operating expenses primarily relating to the clinical trials. During the three months ended March 31, 2017 we used $12.1 million in cash in our operations compared to $7.0 million used in operating activities in the three months ended March 31, 2016.
Conference Call
Management will host an investment community conference call on May 10, 2017 at 8:30 a.m. Eastern / 5:30 a.m. Pacific / 3:30 p.m. Israel to discuss these results and answer questions. Shareholders and other interested parties may participate in the conference call by dialing Domestic: 888-438-5519; International: +1-719-457-1506. Conference ID: 2254081. Webcast: http://public.viavid.com/index.php?id=124151
A replay of the call will be accessible two hours after its completion through May 24, 2017 by dialing Domestic: 844-512-2921; International: +1-412-317-6671; Passcode: 2254081. The call will also be archived for 90 days at www.streetevents.com and www.foamixpharma.com.
About Foamix
Foamix is a specialty pharmaceutical company focused on the development and commercialization of proprietary, innovative and differentiated topical drugs for dermatological therapy. Our clinical stage product candidates include FMX101, our novel minocycline foam for the treatment of moderate-to-severe acne, FMX102 for the treatment of impetigo, FMX 103 for the treatment of rosacea and FDX104, our doxycycline foam for the management of acne-like rash induced by EGFRI anticancer drugs.
In addition, we have development and license agreements relating to our technology with various pharmaceutical companies including Bayer HealthCare and others.
Cautionary Note Regarding Forward-Looking Statements
This release includes forward-looking statements within the meaning of Section 27A of the U.S. Securities Act of 1933, as amended, Section 21E of the U.S. Securities Exchange Act of 1934, as amended, and the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements are statements that are not historical facts, such as statements regarding assumptions, expectations, forecasts, beliefs or intentions related to financial results, commercial results, timing and results of clinical trials and U.S. FDA and other regulatory agencies authorizations. Forward-looking statements are based on our current knowledge and our present beliefs and expectations regarding possible future events and are subject to risks, uncertainties and assumptions. Actual results and the timing of events could differ materially from those anticipated in these forward-looking statements as a result of various factors including, but not limited to, unexpected delays, excess costs or unfavorable results of clinical trials, delays or denial in the U.S. FDA approval process, additional competition in the acne market, denial of reimbursement by third party payors or inability to raise additional capital. We discuss many of these risks in greater detail under the heading "Risk Factors" in our most recent Annual Report on Form 20-F (File No. 17625089) filed on February 21, 2017, and elsewhere in that Annual Report. Although we believe these forward-looking statements are reasonable, they speak only as of the date of this announcement and Foamix undertakes no obligation to update publicly such forward-looking statements to reflect subsequent events or circumstances, except as otherwise required by law. Given these risks and uncertainties, you should not rely upon forward-looking statements as predictions of future events.
Finacea(®) is a registered trademark of Bayer Healthcare.
Contact: U.S. Investor Relations
-------- -----------------------
Ilan Hadar, CFO Michael Rice
Foamix Pharmaceuticals Ltd. LifeSci Advisors, LLC
+972-8-9316233 +1-646-597-6979
ilan.hadar@foamixpharma.com mrice@lifesciadvisors.com
FOAMIX PHARMACEUTICALS LTD.
CONSOLIDATED BALANCE SHEETS
(U.S. dollars in thousands, except per share data)
(Unaudited)
March 31 December 31
-------- -----------
2017 2016
---- ----
A s s e t s
CURRENT ASSETS:
Cash and cash
equivalents $26,157 $31,190
Restricted cash 250 250
Short term bank
deposits 38,488 38,351
Investment in
marketable
securities 35,875 43,275
Restricted investment
in marketable
securities 276 261
Accounts receivable:
Trade 2,413 3,236
Other 1,718 438
----- ---
TOTAL CURRENT ASSETS 105,177 117,001
------- -------
NON-CURRENT ASSETS:
Investment in
marketable
securities 17,529 17,532
Restricted investment
in marketable
securities 137 129
Property and
equipment, net 1,084 938
Other 35 35
--- ---
TOTAL NON-CURRENT
ASSETS 18,785 18,634
------ ------
TOTAL ASSETS $123,962 $135,635
======== ========
FOAMIX PHARMACEUTICALS LTD.
CONSOLIDATED BALANCE SHEETS
(U.S. dollars in thousands, except per share data)
(Unaudited)
March 31, December 31,
--------- ------------
2017 2016
---- ----
Liabilities and shareholders' equity
CURRENT LIABILITIES:
Current maturities of bank
borrowing $13 $20
Accounts payable and accruals:
Trade 5,061 2,267
Other 1,873 2,984
----- -----
TOTAL CURRENT LIABILITIES 6,947 5,271
----- -----
LONG-TERM LIABILITIES:
Liability for employee
severance benefits 470 379
--- ---
TOTAL LONG-TERM LIABILITIES 470 379
--- ---
TOTAL LIABILITIES 7,417 5,650
----- -----
COMMITMENTS (Note 6)
SHAREHOLDERS' EQUITY:
Ordinary Shares, NIS 0.16 par
value -authorized: 1,564 1,561
50,000,000 Ordinary Shares as of March 31,
2017
and December 31, 2016; issued and
outstanding: 37,223,485
and 37,167,791 Ordinary Shares as of March
31, 2017
and December 31, 2016, respectively
Additional paid-in capital 204,952 204,052
Accumulated deficit (89,950) (75,566)
Accumulated other
comprehensive loss (21) (62)
--- ---
TOTAL SHAREHOLDERS' EQUITY 116,545 129,985
------- -------
TOTAL LIABILITIES AND
SHAREHOLDERS' EQUITY $123,962 $135,635
======== ========
FOAMIX PHARMACEUTICALS LTD.
CONSOLIDATED STATEMENTS OF OPERATIONS
(U.S. dollars in thousands, except per share data)
(Unaudited)
Three months ended
------------------
March 31,
---------
2017 2016
REVENUES $927 $745
COST OF REVENUES - 31
--- ---
GROSS PROFIT 927 714
OPERATING EXPENSES:
Research and development 12,675 3,566
Selling, general and administrative 2,822 1,710
----- -----
TOTAL OPERATING EXPENSES 15,497 5,276
------ -----
OPERATING LOSS 14,570 4,562
FINANCE INCOME, net (257) (174)
---- ----
LOSS BEFORE INCOME TAX 14,313 4,388
INCOME TAX 71 120
--- ---
NET LOSS FOR THE PERIOD $14,384 $4,508
======= ======
LOSS PER SHARE BASIC AND DILUTED $0.39 $0.15
===== =====
WEIGHTED AVERAGE NUMBER OF SHARES 37,188 30,654
OUTSTANDING USED IN COMPUTATION
OF BASIC AND DILUTED LOSS PER SHARE
IN THOUSANDS
---
FOAMIX PHARMACEUTICALS LTD.
CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
(U.S. dollars in thousands)
(Unaudited)
Three months ended
------------------
March 31,
---------
2017 2016
NET LOSS
OTHER COMPREHENSIVE INCOME: $14,384 $4,508
Net unrealized gains from marketable
securities (6) (156)
Gains on marketable securities reclassified
into net loss - 2
Net unrealized gains on derivative
financial instruments (75) (78)
Gains on derivative financial instruments
reclassified into net loss 40 4
--- ---
TOTAL OTHER COMPREHENSIVE INCOME (41) (228)
--- ----
TOTAL COMPREHENSIVE LOSS $14,343 $4,280
------- ------
FOAMIX PHARMACEUTICALS LTD.
CONSOLIDATED STATEMENTS OF CASH FLOWS
(U.S. dollars in thousands)
(Unaudited)
Three months ended
------------------
March 31,
---------
2017 2016
---- ----
CASH FLOWS FROM OPERATING ACTIVITIES:
Net Loss $(14,384) $(4,508)
Adjustments required to reconcile net loss
to net cash used in
operating activities:
Depreciation and amortization 44 30
Loss from disposal of fixed
assets 102
Changes in marketable securities
and bank deposits, net 96 (2)
Changes in accrued liability for
employee severance benefits, 91 22
net of retirement fund profit
Share-based compensation 766 533
Non-cash finance expenses
(income), net (47) 2
Changes in operating asset and liabilities:
Increase in trade and other
receivable (392) (2,346)
Increase (decrease) in accounts
payable and accruals 1,671 (759)
----- ----
Net cash used in operating
activities (12,053) (7,028)
------- ------
CASH FLOWS FROM INVESTING ACTIVITIES:
Purchase of fixed assets (280) (115)
Investment in bank deposits (13,207) (13,000)
Investment in marketable
securities (2,913) (700)
Proceeds from sale and maturity
of marketable securities and 23,273 21,149
bank deposits
---
Net cash provided by investing
activities 6,873 7,334
----- -----
CASH FLOWS FROM FINANCING ACTIVITIES:
Proceeds from exercise of options 137 -
Payments in respect of bank
borrowings (8) (8)
--- ---
Net cash provided by financing
activities 129 (8)
--- ---
INCREASE (DECREASE) IN CASH, CASH
EQUIVALENTS AND RESTRICTED (5,051) 298
CASH
EFFECT OF EXCHANGE RATE ON CASH,
CASH EQUIVALENTS AND 18 9
RESTRICTED CASH
CASH, CASH EQUIVALENTS AND
RESTRICTED CASH AT BEGINNING OF
THE 31,440 18,795
PERIOD
---
CASH, CASH EQUIVALENTS AND
RESTRICTED CASH AT END OF THE $26,407 $19,102
PERIOD
===
Cash and cash equivalents $26,157 $19,102
Restricted cash 250 -
--- ---
TOTAL CASH, CASH EQUIVALENTS AND
RESTRICTED CASH SHOWN IN $26,407 $19,102
STATEMENT OF CASH FLOWS
===
SUPPLEMENTARY INFORMATION ON INVESTING AND
FINANCING
ACTIVITIES NOT INVOLVING CASH FLOWS -
Property and equipment purchases included
in accounts payable and accruals $-
$39
===
SUPPLEMENTAL DISCLOSURE OF CASH FLOW
INFORMATION:
Cash paid for taxes $- $91
=== ===
Interest received $178 $-
==== ===
Interest paid $*- $*-
=== ===
* Represents an amount less than $1.
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SOURCE Foamix Pharmaceuticals Ltd
