Biora Therapeutics, Inc. (Nasdaq: BIOR), the biotech company
reimagining therapeutic delivery, today provided a corporate update
and reported financial results for the third quarter ended
September 30, 2024. The company will not host a conference
call.
“We’ve made much faster progress than anticipated developing a
smaller BioJet device that is highly desired by pharma companies,”
said Adi Mohanty, Chief Executive Officer of Biora Therapeutics.
“We recently presented initial animal data on our 00-size, clinical
BioJet device. We were able to increase device capacity while
decreasing overall size, giving BioJet the largest payload capacity
of anything in the ingestible injectables category, and further
increasing the number of drugs that can be delivered.”
“The rapid development allowed us to reassess our partnering
strategy, making the decision to shift from a co-development model
to a focus on licensing the 00-size clinical BioJet device. We
expect to pursue licensing agreements within multiple verticals in
the near term, which we believe is preferable to a single
co-development partner for a period of time. There has been
tremendous interest from our pharma collaborators, both existing
and new parties, and our capacity for testing various molecules
during Q1 is starting to fill up. We continue to believe, based on
our extensive engagement with many pharma companies, that BioJet is
the category-leading technology for oral delivery of
macromolecules. We look forward to testing in a more advanced
animal model during Q4 and enabling progress into IND-enabling
studies,” stated Mr. Mohanty.
“Regarding our NaviCap platform, following a successful Phase 1
trial of BT-600, our team has concluded that the results may
support proceeding to a larger clinical trial in ulcerative colitis
patients, instead of the smaller Phase 1B trial we had been
planning. We are working to facilitate the proper regulatory
interactions to determine the next steps for this program,”
continued Mr. Mohanty.
“We are working with our noteholders and investors to
potentially increase the company’s capitalization with the goal of
maintaining our Nasdaq listing status after December 9. We
appreciate the support of many of these investors as they have
continued to provide funds to progress our programs, although their
commitment cannot be guaranteed going forward. We are actively
engaged with many parties regarding strategic alternatives and plan
to provide a more detailed update soon,” stated Mr. Mohanty.
Third Quarter 2024 and Recent Highlights
NaviCap™ Targeted Oral Delivery Platform and BT-600 in
ulcerative colitis
- Presented Phase 1 Clinical
Trial Data at ACG 2024. Biora presented a summary of the
Phase 1 clinical trial results for BT-600 at the American College
of Gastroenterology Annual Meeting, receiving a Presidential Poster
Award from ACG for high quality, novel research. The poster can be
viewed on the company’s website.
BioJet™ Systemic Oral Delivery Platform Preclinical
Development
- Smaller, 00-Size BioJet Clinical Device. Biora
recently announced a smaller version of the BioJet device based on
market research indicating strong patient preference for a smaller,
00-size capsule. The smaller device uses the same core technology
of internal, liquid jet injection that has been proven in over 30
animal studies to date.
- Payload capacity was increased while
decreasing the overall size of the device from a 000-size capsule
to a 00-size. The BioJet device now has a payload capacity of over
300 microliters, enabling delivery of upwards of 50 milligram
doses, even for molecules that are difficult to concentrate, such
as antibodies.
- The 00-size BioJet device is designed
to be more easily tested in non-human primates. It has also been
designed for compatibility with human clinical trial requirements
and ease of automated manufacturing, including sterile fill and
finish. Biora’s clinical and regulatory experience with the NaviCap
platform informed this work and helped to streamline BioJet
development.
- Biora has tested the trigger function
of the 00-size device on the bench as well as in animals, achieving
almost 100% device performance. The company is now conducting
further animal studies to confirm complete device function with a
test molecule.
Other Matters
- Recent Financings.
Biora partially drew down the facility put in place in August with
its lead investors and complemented this funding source with
approximately $4M in equity raises through registered direct and
ATM program routes.
- Nasdaq Compliance.
Biora received an extension to December 9 from Nasdaq to comply
with the market value of securities requirement. No further
extensions are available beyond that date. The company is in active
negotiations with its lead investors to increase the company’s
capitalization.
- Operating Expenses.
Biora recently realigned its resources to focus on its BioJet
program to ensure it can deliver in the short term the results
needed by large pharma collaborators to progress licensing and
partnering discussions. The company was able to reduce operating
expenses and effective operating cash burn by about 40%, to less
than $2.5 million per month on a going forward basis.
Anticipated Milestones
- Biora anticipates sharing data from
additional canine studies with the double-zero size BioJet device
during Q4 2024.
- Biora plans to perform studies of the
double-zero Biora device with its own molecules in non-human
primates during Q4 2024.
- The company anticipates announcing an
additional expanded collaboration agreement to test the double-zero
BioJet device in primates during Q4 2024.
- Testing of collaborators’ molecules in
primates is anticipated to begin in early 2025, with that round of
testing completed during Q1 2025.
Third Quarter 2024 Financial Results
Comparison of Three Months Ended September 30, 2024
and June 30, 2024
Operating expenses were $16.3 million for the three months ended
September 30, 2024, including $1.3 million in non-cash
stock-based compensation expenses, compared to $16.1 million for
the three months ended June 30, 2024, including $1.6 million in
non-cash stock-based compensation expenses.
Net loss was $18.4 million, including non-cash items of $4.0
million attributable to an extinguishment loss and the change in
fair value of warrant and derivative liabilities, and a gain from
discontinued operations of $3.8 million, while net loss per share
was $5.04 for the three months ended September 30, 2024,
compared to net income of $6.5 million, including non-cash items of
$22.8 million attributable to the change in fair value of warrant
and derivative liabilities, while diluted net loss per share was
$0.35 for the three months ended June 30, 2024.
Comparison of Three Months Ended September 30, 2024
and 2023
Operating expenses were $16.3 million for the three months ended
September 30, 2024, including $1.3 million in non-cash
stock-based compensation expenses, compared to $23.3 million for
the three months ended September 30, 2023, including $10.5
million in non-cash stock-based compensation expenses, primarily
attributable to a one-time charge of approximately $9.0 million
related to vesting of employees' restricted stock units (RSUs) in
2023.
Net loss was $18.4 million, net of non-cash items of $4.0
million attributable to the change in fair value of warrant and
derivative liabilities, and a gain from discontinued operations of
$3.8 million, while net loss per share was $5.04 for the three
months ended September 30, 2024, compared to a net loss of
$73.5 million, including non-cash items of $62.2 million
attributable to an inducement loss of $53.2 million and a one-time
stock-based compensation charge noted above, while net loss per
share was $48.89 for the three months ended September 30,
2023.
About Biora TherapeuticsBiora Therapeutics is a
clinical-stage biotech company developing two smart pill-based
therapeutics platforms: the NaviCap™ platform for colon-targeted
treatment of IBD, designed to improve patient outcomes through
treatment at the site of disease in the gastrointestinal tract, and
the BioJet™ platform for oral delivery of large molecules, designed
to replace injection with needle-free, oral
delivery.
For more information, visit bioratherapeutics.com or follow the
company on LinkedIn or Twitter.
Safe Harbor Statement or Forward-Looking
StatementsThis press release contains “forward-looking
statements” within the meaning of the “safe harbor” provisions of
the Private Securities Litigation Reform Act of 1995, which
statements are subject to substantial risks and uncertainties and
are based on estimates and assumptions. All statements, other than
statements of historical facts included in this press release,
including statements concerning the progress and future
expectations and goals of our research and development, preclinical
and clinical trial activities, and partnering and collaboration
efforts with third parties, are forward-looking statements. In some
cases, you can identify forward-looking statements by terms such as
“envision,” “may,” “might,” “will,” “objective,” “intend,”
“should,” “could,” “can,” “would,” “expect,” “anticipate,”
“forward,” “believe,” “design,” “estimate,” “predict,” “projects,”
“projecting,” “potential,” “plan,” “goal(s),” “target,” or the
negative of these terms, and similar expressions intended to
identify forward-looking statements. These statements reflect our
plans, estimates, and expectations, as of the date of this press
release. These statements involve known and unknown risks,
uncertainties and other factors that could cause our actual results
to differ materially from the forward-looking statements expressed
or implied in this press release. Such risks, uncertainties, and
other factors include, among others, our ability to innovate in the
field of therapeutics, our ability to make future FDA filings and
initiate and execute clinical trials on expected timelines or at
all, our ability to obtain and maintain regulatory approval or
clearance of our products on expected timelines or at all, our
plans to research, develop, and commercialize new products, the
unpredictable relationship between preclinical study results and
clinical study results, our expectations regarding allowed patents
or intended grants to result in issued or granted patents, our
expectations regarding opportunities with current or future
pharmaceutical collaborators or partners, our need of and ability
to raise sufficient capital to achieve our business objectives or
continue our operations, our ability to maintain our listing on the
Nasdaq Global Market or other Nasdaq market by regaining compliance
by the December 9 deadline, the fact that delisting from the Nasdaq
Global Market is a “fundamental change” under the indentures for
our convertible notes triggering an obligation to offer to
repurchase the convertible notes, the fact that we do not have cash
sufficient to repurchase the notes if the noteholders accept such
an offer, and those risks described in “Risk Factors” and
“Management’s Discussion and Analysis of Financial Condition and
Results of Operations” in our Annual Report on Form 10-K for the
year ended December 31, 2023 filed with the Securities and Exchange
Commission (SEC) and other subsequent documents, including
Quarterly Reports on Form 10-Q, that we file with the SEC.
Biora Therapeutics expressly disclaims any obligation to update
any forward-looking statements whether as a result of new
information, future events or otherwise, except as required by
law.
Investor ContactChuck PadalaManaging Director,
LifeSci AdvisorsIR@bioratherapeutics.com(646) 627-8390
Media ContactLiz RobinsonCG
lifelrobinson@cglife.com
Biora Therapeutics, Inc. |
Condensed Consolidated Statements of
Operations |
(Unaudited) |
(In thousands, except share and per share
amounts) |
|
|
|
Three Months Ended |
|
|
|
September 30,2024 |
|
|
June 302024 |
|
Revenues |
|
$ |
32 |
|
|
$ |
318 |
|
Operating expenses: |
|
|
|
|
|
|
Research and development |
|
|
5,610 |
|
|
|
7,704 |
|
Selling, general and administrative |
|
|
10,649 |
|
|
|
8,400 |
|
Total operating expenses |
|
|
16,259 |
|
|
|
16,104 |
|
Loss
from operations |
|
|
(16,227 |
) |
|
|
(15,786 |
) |
Interest expense, net |
|
|
(2,016 |
) |
|
|
(711 |
) |
Gain on warrant liabilities |
|
|
8,260 |
|
|
|
13,003 |
|
Other (expense) income, net |
|
|
(12,279 |
) |
|
|
9,892 |
|
(Loss) income before income taxes |
|
|
(22,262 |
) |
|
|
6,398 |
|
Income
tax benefit |
|
|
(44 |
) |
|
|
(67 |
) |
(Loss) income from continuing operations |
|
|
(22,218 |
) |
|
|
6,465 |
|
Gain from discontinued operations |
|
|
3,816 |
|
|
|
— |
|
Net (loss) income |
|
$ |
(18,402 |
) |
|
$ |
6,465 |
|
Net
(loss) gain per share from continuing operations: |
|
|
|
|
|
|
Basic |
|
$ |
(6.08 |
) |
|
$ |
1.81 |
|
Diluted |
|
$ |
(6.08 |
) |
|
$ |
(0.35 |
) |
Net gain
per share from discontinued operations: |
|
|
|
|
|
|
Basic |
|
$ |
1.04 |
|
|
$ |
— |
|
Diluted |
|
$ |
1.04 |
|
|
$ |
— |
|
Net
(loss) gain per share: |
|
|
|
|
|
|
Basic |
|
$ |
(5.04 |
) |
|
$ |
1.81 |
|
Diluted |
|
$ |
(5.04 |
) |
|
$ |
(0.35 |
) |
Weighted
average shares outstanding: |
|
|
|
|
|
|
Basic |
|
|
3,652,862 |
|
|
|
3,572,017 |
|
Diluted |
|
|
3,652,862 |
|
|
|
7,421,597 |
|
Biora Therapeutics, Inc. |
Condensed Consolidated Statements of
Operations |
(Unaudited) |
(In thousands, except share and per share
amounts) |
|
|
|
Three Months
EndedSeptember 30, |
|
|
|
2024 |
|
|
2023 |
|
Revenues |
|
$ |
32 |
|
|
$ |
— |
|
Operating expenses: |
|
|
|
|
|
|
Research and development |
|
|
5,610 |
|
|
|
10,547 |
|
Selling, general and administrative |
|
|
10,649 |
|
|
|
12,774 |
|
Total operating expenses |
|
|
16,259 |
|
|
|
23,321 |
|
Loss
from operations |
|
|
(16,227 |
) |
|
|
(23,321 |
) |
Interest expense, net |
|
|
(2,016 |
) |
|
|
(2,592 |
) |
Gain on warrant liabilities |
|
|
8,260 |
|
|
|
4,568 |
|
Other expense, net |
|
|
(12,279 |
) |
|
|
(52,108 |
) |
Loss before income taxes |
|
|
(22,262 |
) |
|
|
(73,453 |
) |
Income
tax (benefit) expense |
|
|
(44 |
) |
|
|
1 |
|
Loss from continuing operations |
|
|
(22,218 |
) |
|
|
(73,454 |
) |
Gain from discontinued operations |
|
|
3,816 |
|
|
|
— |
|
Net loss |
|
$ |
(18,402 |
) |
|
$ |
(73,454 |
) |
Net loss
per share from continuing operations, basic and diluted |
|
$ |
(6.08 |
) |
|
$ |
(48.89 |
) |
Net gain
per share from discontinued operations, basic and diluted |
|
$ |
1.04 |
|
|
$ |
— |
|
Net loss
per share, basic and diluted |
|
$ |
(5.04 |
) |
|
$ |
(48.89 |
) |
Weighted
average shares outstanding, basic and diluted |
|
|
3,652,862 |
|
|
|
1,502,473 |
|
Biora Therapeutics, Inc. |
Condensed Consolidated Balance Sheets |
(Unaudited) |
(In thousands) |
|
|
|
September 30,2024 |
|
|
December 31,2023 |
|
|
|
|
|
|
(1) |
|
Assets |
|
|
|
|
|
|
Current
assets: |
|
|
|
|
|
|
Cash, cash equivalents and restricted cash |
|
$ |
3,196 |
|
|
$ |
15,211 |
|
Income tax receivable |
|
|
868 |
|
|
|
830 |
|
Prepaid expenses and other current assets |
|
|
1,990 |
|
|
|
3,030 |
|
Total current assets |
|
|
6,054 |
|
|
|
19,071 |
|
Property
and equipment, net |
|
|
1,175 |
|
|
|
1,156 |
|
Right-of-use assets |
|
|
1,011 |
|
|
|
1,614 |
|
Other
assets |
|
|
193 |
|
|
|
3,302 |
|
Goodwill |
|
|
6,072 |
|
|
|
6,072 |
|
Total assets |
|
$ |
14,505 |
|
|
$ |
31,215 |
|
Liabilities and Stockholders' Deficit |
|
|
|
|
|
|
Current
liabilities: |
|
|
|
|
|
|
Accounts payable |
|
$ |
6,916 |
|
|
$ |
2,843 |
|
Accrued expenses and other current liabilities |
|
|
21,404 |
|
|
|
17,319 |
|
Warrant liabilities |
|
|
18,688 |
|
|
|
40,834 |
|
Convertible notes, net |
|
|
4,527 |
|
|
|
— |
|
Senior secured convertible notes, net |
|
|
14,344 |
|
|
|
— |
|
Related party senior secured convertible notes, net - current
portion |
|
|
19,721 |
|
|
|
1,976 |
|
Derivative liabilities |
|
|
35,018 |
|
|
|
— |
|
Total current liabilities |
|
|
120,618 |
|
|
|
62,972 |
|
Convertible notes, net |
|
|
— |
|
|
|
9,966 |
|
Senior
secured convertible notes, net |
|
|
— |
|
|
|
14,591 |
|
Related
party senior secured convertible notes, net |
|
|
— |
|
|
|
19,179 |
|
Derivative liabilities |
|
|
— |
|
|
|
22,899 |
|
Other
long-term liabilities |
|
|
516 |
|
|
|
3,029 |
|
Total liabilities |
|
$ |
121,134 |
|
|
$ |
132,636 |
|
Stockholders' deficit: |
|
|
|
|
|
|
Common stock |
|
|
3 |
|
|
|
2 |
|
Additional paid-in capital |
|
|
879,530 |
|
|
|
868,613 |
|
Accumulated deficit |
|
|
(967,084 |
) |
|
|
(950,958 |
) |
Treasury stock |
|
|
(19,078 |
) |
|
|
(19,078 |
) |
Total stockholders' deficit |
|
|
(106,629 |
) |
|
|
(101,421 |
) |
Total liabilities and stockholders' deficit |
|
$ |
14,505 |
|
|
$ |
31,215 |
|
|
|
|
|
|
|
|
|
|
(1) The condensed
consolidated balance sheet data as of December 31, 2023 has
been derived from the audited consolidated financial
statements |
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