Celcuity Reports Third Quarter 2020 Financial
Results
and Recent Business Highlights
- New clinical trial collaborations with pharmaceutical companies
on track to close -
- Cash burn rate steady -
- Cash and cash equivalents of $13.7 million as of September 30,
2020, which is expected to support operations through 2021
-
- Conference Call on Monday, November 9th at 4:30pm (ET)
-
Minneapolis,
Minnesota—November 9, 2020—Celcuity Inc. (Nasdaq:
CELC), a clinical stage biotechnology company translating
discoveries of new cancer sub-types into 3rd generation
diagnostics and expanded therapeutic options for cancer patients,
announced financial results for the third quarter ended September
30, 2020 and summarized recent business progress.
“During
the third quarter, we continued to advance our collaboration
discussions with pharmaceutical companies. We expect to close
several pharmaceutical company collaborations over the next few
months,” said Brian Sullivan, Chairman and Chief Executive
Officer of Celcuity. “Each collaboration will evaluate
different drug combinations in HER2-negative metastatic breast
cancer patients selected with our CELsignia Multipathway Activity
test. The collaborations we expect to close first will evaluate
patients with either hyperactive HER2 signaling tumors or those
with hyperactive c-Met and HER2 signaling tumors. Our discussions
with pharmaceutical companies to evaluate PI3K inhibitors in breast
or ovarian cancer patients with hyperactive PI3K signaling are also
progressing. These discussions are at an earlier stage than those
involving patients with hyperactive HER2 or c-Met signaling. We are
also very excited about the clinical investigators we expect to
partner with to field these trials. They are amongst the most
respected oncology researchers and thought leaders in the
country.
“We
continued to make progress advancing additional new tests during
the quarter. Our goal is to develop new CELsignia tests that
identify RAS pathway driven cancers undetectable with molecular
tests in breast and ovarian cancer. Dysregulated signaling
involving RAS network nodes is responsible for a significant
percentage of all cancers, which has led many pharmaceutical
companies to sponsor research in this area.
“Our
CELsignia platform also provides unique insights into the relative
potency and efficacy of the different therapies targeting RAS
nodes. This enables us to determine the relative superiority of the
different RAS-node approved and investigational targeted therapies,
which will help guide our collaboration activities.
“Finally,
we continue to expect interim results from our FACT-1 and FACT-2
trials in the second half of 2021. However, as you would expect, we
are monitoring the recent increase in COVD-19 related
hospitalizations for potential impact on enrollment activities for
these trials.”
Recent Highlights and Upcoming Milestones
-
Multiple clinical
trial collaborations amongst several major pharmaceutical companies
advancing towards close.
-
Data for two new
CELsignia tests in two different tumor types announced during past
nine months.
-
Expect to complete
development of a CELsignia RAS test for breast cancer patients by
next quarter.
-
Interim results
from the FACT-1 and FACT-2 trials are expected in the second half
of 2021
Third Quarter 2020 Financials
Total
operating expenses were $2.48 million for the third quarter of
2020, compared to $2.09 million for the third quarter of 2019.
Operating expenses for the first nine months of 2020 were $7.0
million, compared to $5.91 million for the first nine months of
2019.
Research
and development (R&D) expenses were $1.96 million for the third
quarter of 2020, compared to $1.71 million for the third quarter of
2019. R&D expenses for the first nine months of 2020 were $5.57
million, compared to $4.77 million for the first nine months of
2019. The approximately $0.80 million increase during the first
nine months of fiscal year 2020, compared to the first nine months
of fiscal year 2019, resulted primarily from a $0.71 million
increase in compensation related expenses, including approximately
$0.45 million of non-cash stock-based compensation expense. In
addition, other research and development expenses increased $0.09
million due to clinical validation and laboratory studies, and
operational and business development activities.
General
and administrative (G&A) expenses were $0.52 million for the
third quarter of 2020, compared to $0.38 million for the third
quarter of 2019. G&A expenses for the first nine months of 2020
were $1.43 million, compared to $1.13 million for the first nine
months of 2019. The approximately $0.30 million increase during
fiscal year 2020, compared to fiscal year 2019, resulted primarily
from a $0.24 million increase in compensation related expenses,
including approximately $0.21 million of non-cash stock-based
compensation. In addition, other general and administrative
expenses increased $0.06 million primarily due to professional fees
associated with being a public company.
Net
loss for the third quarter of 2020 was $2.47 million, or $0.24 per
share, compared to a net loss of $1.98 million, or $0.19 per share,
for the third quarter of 2019. Net loss for the first nine months
of 2020 was $6.92 million, or $0.67 per share, compared to $5.55
million, or $0.54 per share, for the first nine months of 2019.
Non-GAAP adjusted net loss for the third quarter of 2020 was $2.03
million, or $0.20 per share, compared to non-GAAP adjusted net loss
of $1.68 million, or $0.16 per share, for the third quarter of
2019. Non-GAAP adjusted net loss for the first nine months of 2020
was $5.59 million, or $0.54 per share, compared to non-GAAP
adjusted net loss of $4.87 million, or $0.47 per share, for the
first nine months of 2019. Non-GAAP adjusted net loss excludes
stock-based compensation expense. Because this item has no impact
on Celcuity’s cash position, management believes non-GAAP adjusted net loss
better enables Celcuity to focus on cash used in operations.
For a reconciliation of financial measures calculated in accordance
with generally accepted accounting principles in the United States
(GAAP) to non-GAAP financial measures, please see the financial
tables at the end of this press release.
Net
cash used in operating activities for the third quarter of 2020 was
$1.65 million, compared to $1.48 million for the third quarter of
2019.
At
September 30, 2020, Celcuity had cash and cash equivalents of $13.7
million, compared to cash and cash equivalents of $18.7 million at
December 31, 2019.
Conference Call
Management
will host a conference call at 4:30 PM Eastern Time today to
discuss the results. Anyone interested in participating should dial
1-866-831-8616 and use passcode 33954. Participants are asked to
dial in 5 to 10 minutes prior to the start of the
call.
About Celcuity
Celcuity is a clinical stage biotechnology company translating
discoveries of new cancer sub-types into pioneering companion
diagnostics and expanded therapeutic options for cancer patients.
Celcuity’s 3rd
generation diagnostic platform,
CELsignia, analyzes living tumor cells to untangle the complexity
of the cellular activity driving a patient’s cancer. This
allows Celcuity to discover new cancer sub-types molecular
diagnostics cannot detect. Celcuity is driven to improve outcomes
for patients and to transform how pharmaceutical companies define
the patient populations for their targeted therapies. Celcuity is
headquartered in Minneapolis, MN. Further information about
Celcuity can be found at www.celcuity.com.
Forward-Looking Statements
This press release contains statements that constitute
“forward-looking statements.” In some cases, you can
identify forward-looking statements by terminology such as
“may,” “should,” “expects,”
“plans,” “anticipates,”
“believes,” “estimates,”
“predicts,” “potential,”
“intends” or “continue,” and other similar
expressions that are predictions of or indicate future events and
future trends, or the negative of these terms or other comparable
terminology. Forward looking statements in this press release
include, without limitation, expectations with respect to new
clinical trial collaborations and the timing or outcomes of such
collaborations, the use of cash, the discovery of additional cancer
sub-types, the development of additional CELsignia tests, the uses
and breadth of application of CELsignia tests, the outcome of the
FACT 1 and FACT 2 clinical trials, clinical trial patient
enrollment and timing of results, anticipated benefits that
Celcuity’s tests may provide to pharmaceutical companies and
to the clinical outcomes of cancer
patients, and expectations regarding the impact that the COVID-19
pandemic and related economic effects will have on Celcuity’s
business and results of operations. Forward-looking statements are
subject to numerous conditions, many of which are beyond the
control of Celcuity, which include, but are not limited to, the
unknown impact of the COVID-19 pandemic on Celcuity’s
business and those other risks set forth in the Risk Factors
section in Celcuity’s Annual Report on Form 10-K for the year
ended December 31, 2019 filed with the Securities and Exchange
Commission on March 13, 2020. Readers are cautioned not to place
undue reliance on these forward-looking statements, which speak
only as of the date hereof. Celcuity undertakes no obligation to
update these statements for revisions or changes after the date of
this press release, except as required by law.
Contacts:
Celcuity
Inc.
763-392-0123
Celcuity Inc.
Condensed Balance Sheets
|
|
|
|
|
|
|
|
|
Assets
|
|
|
|
Current Assets:
|
|
|
|
Cash
and cash equivalents
|
$13,696,387
|
$18,735,002
|
|
Deposits
|
22,009
|
22,009
|
|
Deferred
transaction costs
|
-
|
28,743
|
|
Payroll
tax receivable
|
190,000
|
190,000
|
|
Prepaid
assets
|
103,610
|
274,600
|
|
Total current assets
|
14,012,006
|
19,250,354
|
|
|
|
|
|
Property
and equipment, net
|
626,271
|
833,463
|
|
Operating
lease right-of-use assets
|
275,696
|
196,983
|
|
Total Assets
|
$14,913,973
|
$20,280,800
|
|
|
|
|
|
Liabilities and Stockholders' Equity:
|
|
|
|
Current Liabilities:
|
|
|
|
Accounts
payable
|
$83,130
|
$142,773
|
|
Finance
lease liabilities
|
5,799
|
5,769
|
|
Operating
lease liabilities
|
189,400
|
178,466
|
|
Accrued
expenses
|
756,873
|
584,319
|
|
Total current liabilities
|
1,035,202
|
911,327
|
|
Finance
lease liabilities
|
9,756
|
14,109
|
|
Operating
lease liabilities
|
107,040
|
57,793
|
|
Total Liabilities
|
1,151,998
|
983,229
|
|
Total Stockholders' Equity
|
13,761,975
|
19,297,571
|
|
Total Liabilities and Stockholders' Equity
|
$14,913,973
|
$20,280,800
|
Celcuity Inc.
Condensed Statements of Operations
(unaudited)
|
|
Three Months Ended
September 30,
|
Nine Months Ended
September 30,
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating expenses:
|
|
|
|
|
|
|
|
|
|
|
|
Research
and development
|
$1,962,610
|
$1,711,597
|
$5,576,250
|
$4,772,286
|
|
General
and administrative
|
517,465
|
379,718
|
1,428,578
|
1,135,251
|
|
Total
operating expenses
|
2,480,075
|
2,091,315
|
7,004,828
|
5,907,537
|
|
Loss
from operations
|
(2,480,075)
|
(2,091,315)
|
(7,004,828)
|
(5,907,537)
|
|
|
|
|
|
|
|
Other
income (expense)
|
|
|
|
|
|
Interest
expense
|
(28)
|
(39)
|
(93)
|
(123)
|
|
Interest
income
|
5,805
|
107,100
|
81,639
|
357,321
|
|
Other
income, net
|
5,777
|
107,061
|
81,546
|
357,198
|
|
Net loss before income taxes
|
(2,474,298)
|
(1,984,254)
|
(6,923,282)
|
(5,550,339)
|
|
Income
tax benefits
|
-
|
-
|
-
|
-
|
|
Net loss
|
$(2,474,298)
|
$(1,984,254)
|
$(6,923,282)
|
$(5,550,339)
|
|
|
|
|
|
|
|
Net
loss per share, basic and diluted
|
$(0.24)
|
$(0.19)
|
$(0.67)
|
$(0.54)
|
|
|
|
|
|
|
|
Weighted
average common shares outstanding, basic and diluted
|
10,273,567
|
10,239,957
|
10,262,636
|
10,217,443
|
Cautionary Statement Regarding Non-GAAP Financial
Measures
This press release contains references to non-GAAP adjusted net
loss and non-GAAP adjusted net loss per share. Management believes
these non-GAAP financial measures are useful supplemental measures
for planning, monitoring, and evaluating operational performance as
they exclude stock-based compensation expense from net loss and net
loss per share. Management excludes this item because it does not
impact Celcuity’s cash position, which management believes
better enables Celcuity to focus on cash used in operations.
However, non-GAAP adjusted net loss and non-GAAP adjusted net loss
per share are not recognized measures under GAAP and do not have a
standardized meaning prescribed by GAAP. As a result,
management’s method of calculating non-GAAP adjusted net loss
and non-GAAP adjusted net loss per share may differ materially from
the method used by other companies. Therefore, non-GAAP adjusted
net loss and non-GAAP adjusted net loss per share may not be
comparable to similarly titled measures presented by other
companies. Investors are cautioned that non-GAAP adjusted net loss
and non-GAAP adjusted net loss per share should not be construed as
alternatives to net loss, net loss per share or other statements of
operations data (which are determined in accordance with GAAP) as
an indicator of Celcuity’s performance or as a measure of
liquidity and cash flows.
Celcuity Inc.
Reconciliation of GAAP Net Loss to Non-GAAP Adjusted Net Loss
and
GAAP Net Loss Per Share to Non-GAAP Adjusted Net Loss Per
Share
|
|
Three Months Ended
September 30,
|
Nine Months Ended
September 30,
|
|
|
|
|
|
|
|
|
|
|
|
|
|
GAAP
net loss
|
$(2,474,298)
|
$(1,984,254)
|
$(6,923,282)
|
$(5,550,339)
|
|
Adjustments:
|
|
|
|
|
|
Stock-based
compensation
|
|
|
|
|
|
Research and development(1)
|
254,537
|
163,343
|
813,099
|
364,902
|
|
General and administrative(2)
|
194,410
|
139,901
|
523,690
|
315,232
|
|
Non-GAAP
adjusted net loss
|
$(2,025,351)
|
$(1,681,010)
|
$(5,586,493)
|
$(4,870,205)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
GAAP
net loss per share - basic and diluted
|
$(0.24)
|
$(0.19)
|
$(0.67)
|
$(0.54)
|
|
Adjustment
to net loss (as detailed above)
|
0.04
|
0.03
|
0.13
|
0.07
|
|
Non-GAAP
adjusted net loss per share
|
$(0.20)
|
$(0.16)
|
$(0.54)
|
$(0.47)
|
|
|
|
|
|
|
|
Weighted
average common shares outstanding, basic and diluted
|
10,273,567
|
10,239,957
|
10,262,636
|
10,217,443
|
(1) Reflects a non-cash charge to operating expense for Research
and Development stock-based compensation.
(2) Reflects a non-cash charge to operating expense for General and
Administrative stock-based compensation.