Unum Therapeutics Inc. (NASDAQ: UMRX), a biopharmaceutical company
focused on developing curative cell therapies for solid tumors,
today announced financial results for the fourth quarter and full
year ended December 31, 2019, and provided corporate updates.
“We recently announced the conclusion of our
Phase 1 ACTR707 programs and restructuring to prioritize our
capabilities and resources towards advancing our preclinical
program, BOXR1030, and BOXR platform aimed at discovering novel
‘bolt-on’ transgenes to help T cells survive longer and perform
better in the solid tumor microenvironment,” said Chuck Wilson
Ph.D., President and Chief Executive Officer of Unum. “While taking
steps internally to advance BOXR1030 and the BOXR platform given
the broad potential we see to improve cell therapies in solid
tumors, we are also taking steps to evaluate external opportunities
as well and in this context, and with alignment from our Board of
Directors, we are also actively seeking strategic alternatives to
maximize shareholder value, including a sale or merger of the
Company at this time.”
Recent Program and Corporate
Highlights
- Announced plans to prioritize
resources towards advancing its preclinical program, BOXR1030, for
the treatment of solid tumor cancers: Unum’s BOXR1030
expresses a glypican-3 (GPC3) targeted CAR and incorporates the
novel transgene glutamic-oxaloacetic transaminase 2 (GOT2) to
improve T cell function in the solid tumor microenvironment by
enhancing T cell metabolism. Unum has initiated formal preclinical
development activities, including preclinical safety testing and
GMP process development, to support filing an IND application for
BOXR1030 in late 2020. As part of this effort, and to conserve
resources for BOXR1030, Unum is concluding its ACTR707 clinical
trials, including the Phase 1 trial (ATTCK-20-03) in combination
with rituximab in relapsed/refractory non-Hodgkin lymphoma and the
Phase 1 trial (ATTCK-34-01) in combination with trastuzumab to
treat advanced HER2+ solid tumor cancers. Unum expects to continue
to leverage its BOXR discovery platform, potentially in
collaboration with partners, to create and develop new BOXR product
candidates to address a broad range of solid tumor
cancers.
- Presented preclinical data for
BOXR1030 at the Society for Immunotherapy of Cancer (SITC) Annual
Meeting (November 6-10): BOXR1030 expresses a glypican-3
(GPC3) targeted chimeric antigen receptor (CAR) with the addition
of the “bolt-on” transgene glutamic-oxaloacetic transaminase 2
(GOT2) to improve T cell function in the TME by enhancing T cell
metabolism. As presented at the SITC conference, expression of the
GOT2 mitochondrial enzyme in BOXR1030 increased the production of
key amino acids and metabolites, improved the anti-oxidant balance
of T cells, and prevented their dysfunction and exhaustion in
preclinical studies using stringent animal xenograft models that
simulate the TME. In vitro, BOXR1030 T cells were resistant to
suppressive TME-like conditions, showing improved T cell
proliferation under both hypoxic and low glucose conditions
compared with control GPC3+ CAR-T cells. In vivo, BOXR1030
demonstrated superior activity compared to the control CAR-T with
treated animals achieving complete tumor regressions under
metabolically challenging conditions. Tumor infiltrating
lymphocytes isolated from the tumors of treated animals revealed
that BOXR1030 cells were more resistant to dysfunction, had fewer
markers of exhaustion, and remained functional as compared to the
control CAR-T cells.
- Entered into a common stock purchase agreement for up
to $25 million with Lincoln Park Capital Fund, LLC
("LPC"): Under the terms of the purchase agreement, Unum
Therapeutics will have the sole discretion to direct LPC to
purchase up to $25 million in shares of its common stock over the
36-month term of the agreement based on the market prices
prevailing at the time of each sale to LPC. Unum Therapeutics
controls the timing and amount of any future sales of its stock,
subject to various limitations including those under the NASDAQ
listing rules, and there is no upper limit as to the price per
share that LPC may pay for future stock issuances under the
purchase agreement. LPC has agreed not to cause or engage in any
direct or indirect short selling or hedging of Unum Therapeutics’
common stock. Unum Therapeutics maintains the right to terminate
the common stock purchase agreement at any time, at its discretion,
without any additional cost or penalty.
- Today announced plans to explore strategic options to
maximize shareholder value. Following a
review of its business, including the status of its development
program, resources and capabilities, the Company has initiated a
process to explore strategic alternatives focused on maximizing
shareholder value. Potential strategic alternatives that may be
evaluated include, but are not limited to, an acquisition, merger,
business combination, in-licensing, or other strategic transaction.
There can be no assurance that this process will result in any such
transaction. Unum Therapeutics has not set a timetable for
completion of this review process and does not intend to comment
further unless or until the Board of Directors has approved a
definitive course of action, the review process is concluded, or it
is determined that other disclosure is appropriate.Ladenburg
Thalmann & Co. Inc. has been engaged to act as Unum
Therapeutics’ strategic financial advisor during this process to
explore and evaluate strategic alternatives to maximize shareholder
value.
Fourth Quarter and Full Year 2019
Financial Results
- Collaboration Revenue:
Collaboration revenues were $15.3 million for the fourth quarter of
2019 and $22.5 million for the year ended December 31, 2019,
compared to collaboration revenue of $3.8 million and $9.7 million,
respectively, for the same periods of 2018. Collaboration revenue,
which includes the recognition of a portion of the upfront
payment received as well as reimbursements of research and
development costs attributed to the Seattle Genetics, Inc.
collaboration agreement, increased during the fourth quarter of
2019 compared to the same period in 2018 as a result of the
recognition of a significant portion of the upfront payment from
Seattle Genetics, Inc., due to the suspension of the Phase 1
ATTCK-17-01 trial in November 2019. The collaboration agreement was
subsequently terminated in January 2020.
- R&D Expenses: Research and
development expenses were $10.4 million for the fourth quarter of
2019 and $43.7 million for the year ended December 31, 2019,
compared to $10.8 million and $38.3 million, respectively, for the
same periods of 2018. Research and development expenses relate
to costs for the Phase 1 trials and preclinical programs, as well
as personnel-related costs to support these programs.
- G&A
Expenses: General and administration
expenses were $2.7 million for the fourth quarter of 2019 and $11.0
million for the year ended December 31, 2019, compared to $2.0
million and $7.5 million, respectively, for the same periods of
2018. The increase is primarily related to increased headcount and
personnel-related costs, as well as expenses required to operate as
a public company.
- Net Loss: Net income attributable to
common stockholders was $2.3 million,
or $0.07 per share, for the fourth quarter of 2019 and a
net loss of $31.8 million, or ($1.04) per share, for the year ended
December 31, 2019, compared to a net loss attributable to common
stockholders of $8.6 million, or ($0.29) per
share, and $34.5 million, or ($1.39) per share, respectively, for
the same periods of 2018.
- Cash and Cash Equivalents: As of December
31, 2019, Unum had cash and cash equivalents of $37.4 million. Unum
believes that its existing cash and cash equivalents will fund
operating expenses and capital expenditure requirements into
mid-2021.
About Unum’s BOXR1030 and BOXR
Platform Unum’s BOXR1030 was discovered from its Bolt-on
Chimeric (BOXR) platform that is designed to discover novel
“bolt-on” transgenes to be co-expressed with CARs, a T-cell
receptor, or ACTR, to help T cells survive longer and perform
better in the solid tumor microenvironment. BOXR candidates consist
of two main components: 1) a targeting receptor that directs the T
cell to attack tumor cells, which may be a traditional CAR
receptor, a T-cell receptor, or Unum’s ACTR receptor, and 2) a
novel “bolt-on” transgene that improves the intrinsic function of
the T cell. Once discovered, BOXR transgenes are designed to be
incorporated into several different types of therapeutic T cells,
including both ACTR T cells and CAR-T cells, to impart new
functionality to T cells.
Unum’s first product candidate selected from the
BOXR platform, BOXR1030, expresses GPC3+ targeted CAR and
incorporates the bolt-on GOT2 transgene to improve T cell function
in the solid tumor microenvironment (TME) by enhancing T cell
metabolism. Preclinical data with BOXR1030 was presented at the
Society for Immunotherapy of Cancer (SITC) Annual Meeting in
November 2019. In preclinical studies, BOXR1030 T cells were
resistant to suppressive TME-like conditions, showing improved T
cell proliferation under both hypoxic and low glucose conditions
compared with control GPC3+ CAR-T cells. In vivo, BOXR1030
demonstrated superior activity compared to the parental CAR-T with
treated animals achieving complete tumor regressions. Tumor
infiltrating lymphocytes isolated from the tumors of treated
animals revealed that BOXR1030 cells were more resistant to
dysfunction and had fewer markers of exhaustion as compared to the
control CAR-T cells.
About Unum TherapeuticsUnum
Therapeutics is a biopharmaceutical company focused on developing
curative cell therapies to treat patients with solid tumor cancers.
Unum’s novel proprietary technology includes BOXR, which is
designed to improve the functionality of engineered T cells by
incorporating a “bolt-on” transgene to overcome resistance of the
solid tumor microenvironment to T cell attack. Unum’s preclinical
program BOXR1030 expresses the GOT2 transgene and targets GPC3+
solid tumor cancers. The Company is headquartered in Cambridge,
MA.
Follow Unum Therapeutics on social media:
@UnumRx, and LinkedIn.
Forward looking Statements
This press release contains forward-looking
statements including, without limitation, statements regarding our
future expectations, plans and prospects, including the Company’s
strategic alternatives review process and the potential
transactions that may be identified and explored as a result of
that process, projections regarding our long-term growth,
enrollment and results for our preclinical and clinical activities,
the development of our product candidate, BOXR1030, and the
anticipated timing and success of any of our preclinical studies,
clinical trials and regulatory filings, and our strategies,
business plans, and focus, as well as other statements containing
the words "anticipate," "believe," "continue," "could," "estimate,"
"expect," "intend," "may," "might," "plan," "potential," "predict,"
"project," "should," "target," "will," or "would" and similar
expressions, constitute forward-looking statements within the
meaning of the safe harbor provisions of The Private Securities
Litigation Reform Act of 1995, as amended. We may not actually
achieve the forecasts disclosed in our forward-looking statements,
and you should not place undue reliance on our forward-looking
statements. Actual results could differ materially from the
projections disclosed in the forward-looking statements we make as
a result of a variety of risks and uncertainties, including risks
related to the ability of the Company to identify and consummate
strategic alternatives that yield additional value for
shareholders; the timing, benefits and outcome of the Company's
strategic alternatives review process, including the determination
of whether or not to pursue or consummate any strategic
alternative; the structure, terms and specific risks and
uncertainties associated with any potential strategic transaction;
potential disruptions in our business and the stock price as a
result of our exploration, review and pursuit of strategic
alternatives or the public announcement thereof and any decision or
transaction resulting from such review; the accuracy of our
estimates regarding expenses, future revenues, capital
requirements, and the need for additional financing, the success,
cost and timing of our product development activities and clinical
trials, our ability to obtain and maintain regulatory approval for
our product candidates, the impact of COVID-19 on our business,
preclinical and clinical activities and strategic alternatives
review, and the other risks and uncertainties described in the
"Risk Factors" sections of our public filings with the Securities
and Exchange Commission. In addition, the forward-looking
statements included in this press release represent our views as of
the date hereof. We anticipate that subsequent events and
developments may cause our views to change. However, while we may
elect to update these forward-looking statements at some point in
the future, we specifically disclaim any obligation to do so. These
forward-looking statements should not be relied upon as
representing our views as of any date subsequent to the date
hereof.
Investor Contact: Stern Investor Relations, Inc. Stephanie
Ascher, 212-362-1200 stephanie@sternir.com
Media Contact:Lissette Steele,
202-930-4762lsteele@vergescientific.com
UNUM THERAPEUTICS INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited, $ in thousands, except share and per share
amounts)
|
|
Year Ended December 31, |
|
3 months ended December 31, |
|
|
|
2019 |
|
|
|
2018 |
|
|
|
2019 |
|
|
|
2018 |
|
Collaboration revenue |
|
$ |
22,499 |
|
|
$ |
9,734 |
|
|
$ |
15,288 |
|
|
$ |
3,805 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
Research and development |
|
|
43,709 |
|
|
|
38,285 |
|
|
|
10,354 |
|
|
|
10,765 |
|
General and administrative |
|
|
10,968 |
|
|
|
7,454 |
|
|
|
2,694 |
|
|
|
2,044 |
|
Total operating expenses |
|
|
54,677 |
|
|
|
45,739 |
|
|
|
13,048 |
|
|
|
12,809 |
|
Loss from operations |
|
|
(32,178 |
) |
|
|
(36,005 |
) |
|
|
2,240 |
|
|
|
(9,004 |
) |
Other income (expense): |
|
|
|
|
|
|
|
|
Interest income |
|
|
267 |
|
|
|
1,153 |
|
|
|
61 |
|
|
|
408 |
|
Other income, net |
|
|
78 |
|
|
|
320 |
|
|
|
(4 |
) |
|
|
(10 |
) |
Total other income, net |
|
|
345 |
|
|
|
1,473 |
|
|
|
57 |
|
|
|
398 |
|
Net loss |
|
|
(31,833 |
) |
|
|
(34,532 |
) |
|
|
2,297 |
|
|
|
(8,606 |
) |
Accretion of redeemable
convertible preferred stock to redemption value |
|
|
— |
|
|
|
(16 |
) |
|
|
— |
|
|
|
— |
|
Net loss attributable to common
stockholders |
|
$ |
(31,833 |
) |
|
$ |
(34,548 |
) |
|
$ |
2,297 |
|
|
$ |
(8,606 |
) |
Net loss per share attributable
to common stockholders, basic |
|
$ |
(1.04 |
) |
|
$ |
(1.39 |
) |
|
$ |
0.07 |
|
|
$ |
(0.29 |
) |
Weighted average common shares
outstanding, basic |
|
|
30,480,330 |
|
|
|
24,895,670 |
|
|
|
30,663,054 |
|
|
|
30,018,342 |
|
Net loss per share attributable
to common stockholders, diluted |
|
$ |
(1.04 |
) |
|
$ |
(1.39 |
) |
|
$ |
0.07 |
|
|
$ |
(0.29 |
) |
Weighted average common shares
outstanding, diluted |
|
|
30,480,330 |
|
|
|
24,895,670 |
|
|
|
31,195,620 |
|
|
|
30,018,342 |
|
UNUM THERAPEUTICS INC. CONSOLIDATED
SELECTED BALANCE SHEET DATA (unaudited, in thousands)
|
|
December 31, 2019 |
|
|
December 31, 2018 |
|
Cash, cash equivalents and
marketable securities |
|
$ |
37,424 |
|
|
$ |
78,594 |
|
Working capital |
|
$ |
27,343 |
|
|
$ |
56,057 |
|
Total assets |
|
$ |
49,423 |
|
|
$ |
85,927 |
|
Total liabilities |
|
$ |
17,661 |
|
|
$ |
25,693 |
|
Total stockholders’ equity |
|
$ |
31,762 |
|
|
$ |
60,234 |
|
Unum Therapeutics (NASDAQ:UMRX)
Historical Stock Chart
From Oct 2024 to Nov 2024
Unum Therapeutics (NASDAQ:UMRX)
Historical Stock Chart
From Nov 2023 to Nov 2024