Biocept, Inc. (Nasdaq: BIOC), a leading provider of molecular
diagnostic assays, products and services, reports financial results
for the three and six months ended June 30, 2023 and provides a
business update.
“Biocept’s primary focus is establishing our proprietary
cerebrospinal fluid assay CNSide™ as standard of care. We continue
to diligently work towards submission to the National Comprehensive
Cancer Network® (NCCN®) for consideration to include CNSide in
their standard-of-care guidelines. We believe securing this status
will broaden physician adoption and support reimbursement that
reflects our test’s value in clinical decision-making,” said
Antonino Morales, Biocept President and CEO. “Our ongoing FORESEE
clinical trial is powered to generate data in support of this goal
by assessing CNSide’s impact on physicians’ treatment decisions.
I’m exceptionally pleased that patient enrollment in FORESEE has
passed the midpoint, with four clinical sites open around the
country for patient recruitment and several additional medical
centers expected to join in the coming weeks.
“We plan to provide further evidence of CNSide’s clinical
utility through publication in peer-reviewed medical journals. We
have submitted a manuscript with a description of our assay and its
features, validation from pilot studies and compelling case studies
showing actual use in patient management. Four additional
manuscripts are being prepared in collaboration with leading
neuro-oncologists for submission to scientific journals, including
several documenting their clinical experiences with CNSide in their
practices,” Mr. Morales continued.
“We right sized our business to align with our primary focus,
which is helping to extend our cash runway. Progressing towards
standard of care, completing the FORESEE clinical trial, and
reducing expenses are key to Biocept becoming a self-sustaining
business,” Mr. Morales added.
Earlier today Biocept announced that Priya U. Kumthekar, MD, a
United Counsel for Neurologic Subspecialties (UCNS)-certified
neuro-oncologist at Northwestern University, and David Piccioni,
MD, PhD, Director of Neuro-Oncology at University of California,
San Diego, discussed the use of CNSide in presentations at the 2023
SNO/ASCO CNS Cancer Conference, which was held last week.
Biocept intends to host a business update call later in August
to present a progress report on the FORESEE trial and discuss other
recent developments. Details of the call will be announced in a
press release.
Second Quarter Financial Results
Net revenues for the second quarter of 2023 were $0.6 million,
compared with $5.8 million for the second quarter of 2022, with the
decline due to lower RT-PCR COVID-19 testing volume. As previously
reported, the Company ceased providing COVID-19 testing services in
February 2023. The number of commercial accessions delivered for
the second quarters of 2023 and 2022 were 322 and 77,779,
respectively.
Cost of revenues for the second quarter of 2023 was $2.6
million, compared with $8.0 million for the second quarter of 2022,
with the decrease primarily due to the cessation of COVID-19
testing services and reduced headcount.
Research and development (R&D) expenses for the second
quarter of 2023 were $0.4 million, compared with $1.7 million for
the second quarter of 2022, with the decrease primarily due to a
reduction in headcount and lower purchases of materials and
supplies.
General and administrative (G&A) expenses for the second
quarter of 2023 were $3.5 million, compared with $4.3 million for
the second quarter of 2022. The decrease was primarily due to lower
headcount and consulting fees.
Sales and marketing expenses for the second quarter of 2023 were
$0.3 million, compared with $1.7 million for the second quarter of
2022, with the decrease primarily due to a reduction in headcount,
and lower consulting, promotion and outside service-related
expenses.
Non-cash change in the fair value of warrant liability for the
second quarter of 2023 was $2.4 million. There was no comparable
item for the second quarter of 2022.
Net loss attributable to common stockholders for the second
quarter of 2023 was $3.6 million, or $3.50 per share, compared with
a net loss attributable to common stockholders for the second
quarter of 2022 of $10.0 million, or $17.82 per share.
Six Month Financial Results
Net revenues for the first half of 2023 were $1.3 million,
compared with $25.8 million for the first half of 2022.
Operating expenses for the first half of 2023 were $14.5
million, and included cost of revenues of $5.6 million, R&D
expenses of $1.4 million, G&A expenses of $6.5 million and
sales and marketing expenses of $1.0 million.
Net loss attributable to common stockholders for the first half
of 2023 was $10.8 million, or $13.25 per share, compared with net
loss attributable to common stockholders for the first half of 2022
of $12.3 million, or $21.78 per share.
Biocept reported cash of $6.6 million as of June 30, 2023,
compared with $12.9 million as of December 31, 2022. In May 2023,
the Company received net cash proceeds of approximately $3.6
million from an underwritten public offering, after deducting
underwriting discounts and other expenses payable by the
Company.
About the FORESEE Clinical Trial
The multi-center, prospective FORESEE clinical trial is a
longitudinal therapy response monitoring study in subjects with
leptomeningeal metastases (LM) using CNSide™ (CSF Tumor Cells)
compared to standard of care (CSF cytology, clinical evaluation,
and imaging). The goal of the FORESEE trial is to evaluate the
performance of CNSide in monitoring the response of LM to treatment
and to assess the impact of CNSide on treatment decisions made by
physicians. The trial is enrolling up to 40 patients with breast or
non-small cell lung cancer (NSCLC) who have suspected or confirmed
LM. Standard of care methods to diagnose or assess the treatment
response of LM have limited sensitivity and specificity. This
creates challenges for physicians to manage LM or determine the
best course of treatment. CNSide is a Laboratory Developed Test
(LDT) that is used commercially at the physician’s discretion in
Biocept’s CLIA-certified, CAP-accredited laboratory.
About Biocept
Biocept is a molecular diagnostics company with commercialized
assays for patients with carcinomas or melanomas. Our experts have
spent years working to change the way physicians look at
cerebrospinal fluid in cancer patients. Biocept has developed a
unique, patented methodology to isolate cancer material that is
shed from the primary tumor, such as CSF tumor cells (CSF-TCs) and
cell-free DNA (cfDNA). As such, Biocept is a leading commercial
provider of testing services designed to enable clinicians to
rapidly detect and monitor cancer biomarkers from a cerebrospinal
fluid sample.
Forward-Looking Statements Disclaimer Statement
This news release contains forward-looking statements that are
based upon current expectations or beliefs, as well as a number of
assumptions about future events. Although we believe that the
expectations reflected in the forward-looking statements and the
assumptions upon which they are based are reasonable, we can give
no assurance that such expectations and assumptions will prove to
be correct. Forward-looking statements are generally identifiable
by the use of words like "will," "expect," “goal,” “objective,”
"believe" or "intend" or the negative of these words or other
variations on these words or comparable terminology. To the extent
that statements in this news release are not strictly historical,
including, without limitation, statements regarding FORESEE’s
potential to generate evidence of CNSide’s clinical utility to
support adoption into clinical care guidelines and broaden
physician adoption and support reimbursements, our expectation that
several additional medical centers will join the FORESEE clinical
trial in the coming weeks, our plan to provide further evidence of
CNSide’s clinical utility through publication in peer-reviewed
medical journals, additional manuscripts to be submitted for peer
review, our cash runway, and other statements that are not
historical fact, are forward-looking, and are made pursuant to the
safe harbor provisions of the Private Securities Litigation Reform
Act of 1995. The reader is cautioned not to put undue reliance on
these forward-looking statements, as these statements are subject
to numerous risks and uncertainties, including that the results of
the FORESEE clinical trial may not support the inclusion of CNSide
in clinical care guidelines; Medicare and private payors may not
provide coverage and reimbursement or may breach, rescind or modify
their contracts or reimbursement policies or delay payments; risks
related to our need for additional capital; and the risk that our
products and services may not perform as expected. These and other
factors are described in greater detail under the "Risk Factors"
heading in our Quarterly Report on Form 10-Q for the quarter ended
March 31, 2023, filed with the Securities and Exchange Commission
(SEC) on May 10, 2023, and in our Quarterly Report on Form 10-Q for
the quarter ended June 30, 2023, being filed with the SEC today.
The effects of such risks and uncertainties could cause actual
results to differ materially from the forward-looking statements
contained in this news release. We do not plan to update any such
forward-looking statements and expressly disclaim any duty to
update the information contained in this press release except as
required by law. Readers are advised to review our filings with the
SEC at http://www.sec.gov/.
Biocept, Inc.
Condensed Balance
Sheets
(In thousands, except share
and per share data)
June 30,
December 31,
2023
2022
Assets
(unaudited)
Current assets:
Cash
$
6,633
$
12,897
Accounts receivable
800
2,151
Inventories, net
551
757
Prepaid expenses and other current
assets
876
538
Total current assets
8,860
16,343
Fixed assets, net
2,395
2,572
Lease right-of-use asset - operating
8,190
8,486
Lease right-of-use assets - finance
2,272
3,086
Other non-current assets
386
386
Total assets
$
22,103
$
30,873
Liabilities and
Stockholders' Equity
Current liabilities:
Accounts payable
$
1,467
$
1,523
Accrued liabilities
1,529
2,249
Current portion of lease liability -
operating
565
518
Current portion of lease liabilities -
finance
815
1,099
Financed insurance premiums
526
117
Total current liabilities
4,902
5,506
Non-current portion of lease liability -
operating
8,849
9,175
Non-current portion of lease liabilities -
finance
836
1,200
Payor liability
6,149
6,132
Warrant liability
1,077
—
Total liabilities
21,813
22,013
Commitments and contingencies
Stockholders’ equity:
Preferred stock, $0.0001 par value,
5,000,000 shares authorized; 2,090 shares issued and outstanding at
June 30, 2023 and December 31, 2022
—
—
Common stock, $0.0001 par value,
150,000,000 shares authorized; 2,407,381 shares and 568,994 shares
issued and outstanding at June 30, 2023 and December 31, 2022,
respectively.
—
—
Additional paid-in capital
309,503
307,298
Accumulated deficit
(309,213
)
(298,438
)
Total stockholders’ equity
290
8,860
Total liabilities and stockholders’
equity
$
22,103
$
30,873
Biocept, Inc.
Condensed Statements of
Operations
(In thousands, except shares
and per share data)
(Unaudited)
For the Three Months Ended
June 30,
For the Six Months Ended June
30,
2023
2022
2023
2022
Net revenues
$
589
$
5,819
$
1,262
$
25,763
Costs and expenses:
Cost of revenues
2,550
8,023
5,578
18,357
Research and development expenses
409
1,729
1,449
3,574
General and administrative expenses
3,494
4,300
6,482
10,556
Sales and marketing expenses
250
1,656
965
5,314
Total costs and expenses
6,703
15,708
14,474
37,801
Loss from operations
(6,114
)
(9,889
)
(13,212
)
(12,038
)
Other income (expense):
Interest expense, net
(50
)
(155
)
(96
)
(217
)
Other income, net
91
—
91
—
Change in fair value of warrant
liability
2,442
—
2,442
—
Total other income (expense):
2,483
(155
)
2,437
(217
)
Loss before income taxes
(3,631
)
(10,044
)
(10,775
)
(12,255
)
Income tax expense
—
—
—
—
Net loss
(3,631
)
(10,044
)
(10,775
)
(12,255
)
Net loss attributable to common
stockholders
$
(3,631
)
$
(10,044
)
$
(10,775
)
$
(12,255
)
Weighted-average shares outstanding used
in computing net loss per share attributable to common
stockholders:
Basic
1,036,529
563,528
813,180
562,561
Diluted
1,036,529
563,528
813,180
562,561
Net loss per common share:
Basic
$
(3.50
)
$
(17.82
)
$
(13.25
)
$
(21.78
)
Diluted
$
(3.50
)
$
(17.82
)
$
(13.25
)
$
(21.78
)
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Investor & Media
Contact: LHA Investor Relations Jody Cain Jcain@lhai.com
(310) 691-7100
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