Unum Therapeutics Reports First Quarter Financial Results and Provides Corporate Updates
May 11 2020 - 4:30PM
Unum Therapeutics Inc. (NASDAQ: UMRX), a biopharmaceutical company
focused on developing curative cell therapies for solid tumors,
today announced financial results for the first quarter ended March
31, 2020, and provided corporate updates.
Recent Program and Corporate
Highlights
- Announced plans to prioritize
resources towards advancing its preclinical program, BOXR1030, for
the treatment of solid tumor cancers: On March 2nd, Unum
announced a corporate restructuring plan 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 cGMP
manufacturing readiness activities, to support filing an
investigational new drug (IND) application for BOXR1030 in late
2020.
- 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
announced on March 20th, 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.
- Exploring strategic options to maximize shareholder
value: Following a review of its business, the
Company recently initiated and continues a process to explore
strategic alternatives focused on maximizing shareholder value,
with Ladenburg Thalmann & Co. Inc. acting as Unum Therapeutics’
strategic financial advisor during this process. 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.
First Quarter 2020 Financial
Results
- Collaboration Revenue:
Collaboration revenue recognized during the first quarter ended
March 31, 2020 of $7.0 million compared to $3.1 million in the same
period of 2019. Collaboration revenue includes the recognition of a
portion of the upfront payment received from Seattle Genetics,
Inc. as reimbursements for research and development costs, and
increased during the quarter ended March 31, 2020 as a result of
the conclusion of the ATTCK-17-01 Phase 1 clinical trial and the
termination of the collaboration agreement.
- R&D Expenses: Research and
development expenses of $9.5 million for the first quarter
ended March 31, 2020 compared to $12.4 million for the same
period of 2019. Research and development expenses relate to
ongoing costs for Phase 1 trials and the BOXR1030 preclinical
program, as well as personnel-related costs to support these
programs.
- G&A
Expenses: General and administrative
expenses for the first quarter ended March 31, 2020 were $3.7
million, compared to $2.5 million for the same period of 2019.
The increase is primarily related to increased personnel-related
costs, including severance costs, as well as expenses required to
operate as a public company.
- Net Loss: Net loss attributable to common
stockholders was $6.1 million, or $0.20 per
share, for the first quarter ended March 31, 2020 compared with a
net loss attributable to common stockholders of $11.7 million,
or $0.39 per share, for the same period of
2019.
- Cash and Cash Equivalents: As of March
31, 2020, Unum had cash and cash equivalents of $29.6 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.
UNUM THERAPEUTICS INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited, $ in thousands, except share and per share
amounts)
|
|
Three Months Ended March 31, |
|
|
|
2020 |
|
|
2019 |
|
Collaboration revenue |
|
$ |
7,031 |
|
|
$ |
3,053 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
Research and development |
|
|
9,498 |
|
|
|
12,403 |
|
General and administrative |
|
|
3,674 |
|
|
|
2,491 |
|
Total operating expenses |
|
|
13,172 |
|
|
|
14,894 |
|
Loss from operations |
|
|
(6,141 |
) |
|
|
(11,841 |
) |
Other income (expense): |
|
|
|
|
|
|
|
|
Interest income |
|
|
47 |
|
|
|
150 |
|
Total other income (expense), net |
|
|
47 |
|
|
|
150 |
|
Net loss |
|
$ |
(6,094 |
) |
|
$ |
(11,691 |
) |
Net loss per common share, basic
and diluted |
|
$ |
(0.20 |
) |
|
$ |
(0.39 |
) |
Weighted average common shares
outstanding, basic and diluted |
|
|
30,136,749 |
|
|
|
30,083,006 |
|
|
UNUM THERAPEUTICS INC. CONSOLIDATED
SELECTED BALANCE SHEET DATA (unaudited, in thousands)
|
|
March 31, 2020 |
|
|
December 31, 2019 |
|
Cash, cash equivalents and marketable securities |
|
$ |
29,604 |
|
|
$ |
37,424 |
|
Working capital |
|
$ |
21,935 |
|
|
$ |
27,343 |
|
Total assets |
|
$ |
38,939 |
|
|
$ |
49,423 |
|
Total liabilities |
|
$ |
13,237 |
|
|
$ |
17,661 |
|
Total stockholders’ equity |
|
$ |
25,702 |
|
|
$ |
31,762 |
|
Media Contact:
Lissette Steele, 202-930-4762
lsteele@vergescientific.com
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