Kronos Bio Reports Recent Business Progress and Fourth-Quarter and Full-Year 2023 Financial Results
March 21 2024 - 7:05AM
Kronos Bio, Inc. (Nasdaq: KRON), a company dedicated to
transforming the lives of those affected by cancer, today reported
recent business progress and fourth-quarter and full-year 2023
financial results.
“In 2023, we made great progress across our
portfolio and business. We demonstrated that KB-0742 has a safety
profile that is clearly differentiated from all other CDK9
inhibitors, and we believe our extended dosing schedule will show
increased efficacy signals while maintaining a favorable safety
profile,” said Nobert Bischofberger, Ph.D., president and chief
executive officer of Kronos Bio. “We also announced our second
development candidate, KB-9558, which is designed to target the KAT
domain of p300 and downregulate IRF4 transcription in multiple
myeloma. We are looking forward to completing the IND-enabling
studies in 2024 and expect to dose our first patients in the first
half of 2025.”
Clinical Program and Recent Company
Updates
KB-0742
- At the 2023 AACR-NCI-EORTC
International Conference, the Company reported target engagement,
tumor regressions, and an acceptable safety profile for KB-0742
dosed at 60mg three-days-on, four-days-off in heavily pre-treated
patients with transcriptionally addicted solid tumors. Out of
fourteen “all-comer” patients, two patients with myxoid liposarcoma
exhibited tumor regressions: one (7th line) had a partial response
(per RECIST v1.1) lasting 113 days and the second achieved a 26%
reduction in tumor diameters with stable disease. KB-0742 also
cleared the 80mg three-days-on, four-days-off schedule in dose
escalation and is currently enrolling patients in the KB-0742 60mg
four-days-on, three-days-off dose escalation cohort of the Phase
1/2 trial.
- At a medical conference in
mid-2024, the Company intends to share an update on the clinical
data to date from patients with transcriptionally addicted tumors
who were dosed with 60mg three-days-on, four-days-off, and from
“all-comer” patients in the dose-escalation cohort who received
80mg three-days-on, four-days-off.
- In the third quarter of 2024, the
Company expects to clear the 80mg four-days-on, three-days-off dose
escalation cohort, and begin enrolling patients in an expansion
cohort including one or more of the following: non-small cell lung
cancer, small cell lung cancer, ovarian cancer, and triple negative
breast cancer.
- The Company expects to announce
topline data from the expansion cohort at the 80mg four-days-on,
three-days-off dose in the first half of 2025.
KB-9558
- In December 2023, the Company
announced the nomination of KB-9558, a p300 KAT inhibitor, as a
development candidate.
- KB-9558 is the second development
candidate to emerge from Kronos Bio’s product engine, where the
Company identified that inhibition of the lysine acetyltransferase
(KAT) domain on p300 inhibits expression of interferon regulatory
factor 4 (IRF4) and thus collapses the transcription regulatory
network that is required for the survival of multiple myeloma
cells.
- The Company plans to present data
on KB-9558 at the American Association for Cancer Research (AACR)
annual meeting, being held from April 5-10, 2024 in San Diego,
California, including how targeting p300’s enzymatic KAT domain can
selectively downregulate IRF4.
- Pending completion of IND-enabling
studies in 2024, the Company intends to initiate a first-in-human
trial in relapsed or refractory multiple myeloma in the first half
of 2025.
Lanraplenib
- In December 2023, after a review of
data from the Phase 1b portion of its Phase 1b/2 trial of
lanraplenib in combination with gilteritinib in FLT3-mutated
relapsed/refractory acute myeloid leukemia (AML), the Company
decided not to proceed to Phase 2.
Company Update
- Kronos Bio extended its expected
cash runway by a year, into the second half of 2026, through
restructurings and resource optimization.
Fourth-Quarter and Full-Year 2023
Financial Highlights
- Cash, Cash Equivalents and Investments: With
its ongoing and currently planned clinical programs and $175.0
million in cash, cash equivalents and investments as of
December 31, 2023, the Company anticipates sufficient
resources to fund its planned operations into the second half of
2026.
- R&D Expenses:
Research and development expenses were $18.7 million for the fourth
quarter of 2023, which includes non-cash stock-based compensation
expense of $2.5 million. For the full year of 2023, research and
development expenses were $86.4 million, which includes non-cash
stock-based compensation expense of $12.0 million.
- G&A Expenses:
General and administrative expenses were $10.9 million for the
fourth quarter of 2023, which includes non-cash stock-based
compensation expense of $2.7 million. For the full year of 2023,
general and administrative expenses were $41.7 million, which
includes non-cash stock-based compensation expense of $13.0
million.
- Net Loss: Net loss
for the fourth quarter of 2023 was $25.3 million, or $0.43 per
share, including non-cash stock-based compensation expense of $5.2
million. Net loss for the full-year 2023 was $112.7 million, or
$1.95 per share, including non-cash stock-based compensation
expense of $25.0 million.
About Kronos Bio, Inc.
Kronos Bio is a biopharmaceutical company that
is advancing an investigational CDK9 inhibitor compound, KB-0742,
in a Phase 1/2 clinical trial as a treatment for MYC-amplified
solid tumors and other transcriptionally addicted solid tumors as
well as a preclinical development candidate, KB-9558, targeting the
KAT domain of p300 for multiple myeloma. The Company’s scientific
focus is on developing medicines that target deregulated
transcription, the hallmark of cancer and other serious
diseases.
Kronos Bio is based in San Mateo, Calif., and
has a research facility in Cambridge, Mass. For more information,
visit https://www.kronosbio.com/ or follow the Company on
LinkedIn.
Forward-Looking Statements
Statements in this press release that are not
statements of historical fact are forward-looking statements for
purposes of the safe harbor provisions of the Private Securities
Litigation Reform Act of 1995. The press release, in some cases,
uses terms such as “anticipate,” “believe,” “could,” “expect,” “on
track,” “plan,” “potential,” “promising,” “will,” or other words
that convey uncertainty of future events or outcomes to identify
these forward-looking statements. Forward-looking statements
include statements regarding Kronos Bio’s intentions, beliefs,
projections, outlook, analyses or current expectations concerning,
among other things, the Phase 1/2 study of KB-0742 being on track
to clear 80mg four-days-on, three-days-off schedule in Q3 2024;
expected clinical results from the KB-0742 study; the expected
timing for additional clinical data from the Phase 1/2 KB-0742
study; the potential completion of IND-enabling studies and the
initial of a clinical trial for KB-9558 and the timing thereof;
future pipeline development activities or outcomes; the potential
of Kronos Bio’s product candidates; Kronos Bio’s expected cash
runway; and other statements that are not historical fact. Actual
results and the timing of events could differ materially from those
anticipated in such forward-looking statements as a result of
various risks and uncertainties, including, without limitation:
risks associated with changes to the assumptions underlying
estimated expenses and savings; changes in the macroeconomic
environment or competitive landscape that impact Kronos Bio’s
business; whether Kronos Bio will be able to progress its clinical
trials on the timelines anticipated, including due to risks
inherent in the clinical development of novel therapeutics; risks
related to Kronos Bio’s limited experience as a company in
conducting clinical trials; the risk that results of preclinical
studies and early clinical trials (including preliminary results)
are not necessarily predictive of future results; and risks
associated with the sufficiency of Kronos Bio’s cash resources and
need for additional capital. These and other risks are described in
greater detail in Kronos Bio’s filings with the Securities and
Exchange Commission (SEC), including under the heading “Risk
Factors” in its Quarterly Report on Form 10-Q for the quarter ended
September 30, 2023, filed with the SEC on November 13, 2023, and in
its Annual Report on Form 10-K for the year ended December 31,
2023, being filed with the SEC today. Any forward-looking
statements that are made in this press release speak only as of the
date of this press release and are based on management’s
assumptions and estimates as of such date. Except as required by
law, Kronos Bio assumes no obligation to update the forward-looking
statements whether as a result of new information, future events or
otherwise, after the date of this press release.
Kronos Bio, Inc.Statements of Operations
and Comprehensive Loss(in thousands, except per share
data)(Unaudited) |
|
|
Three Months Ended December 31, |
|
Year Ended December 31, |
|
|
2023 |
|
|
|
2022 |
|
|
|
2023 |
|
|
|
2022 |
|
Revenue |
$ |
2,286 |
|
|
$ |
— |
|
|
$ |
6,288 |
|
|
$ |
— |
|
Operating expenses: |
|
|
|
|
|
|
|
Research and development |
|
18,704 |
|
|
|
23,168 |
|
|
|
86,379 |
|
|
|
93,715 |
|
General and administrative |
|
10,926 |
|
|
|
10,514 |
|
|
|
41,739 |
|
|
|
43,400 |
|
Total operating expenses |
|
29,630 |
|
|
|
33,682 |
|
|
|
128,118 |
|
|
|
137,115 |
|
Loss from operations |
|
(27,344 |
) |
|
|
(33,682 |
) |
|
|
(121,830 |
) |
|
|
(137,115 |
) |
Other income (expense),
net: |
|
|
|
|
|
|
|
Interest and other income, net |
|
2,024 |
|
|
|
1,900 |
|
|
|
9,157 |
|
|
|
3,911 |
|
Total other income (expense),
net |
|
2,024 |
|
|
|
1,900 |
|
|
|
9,157 |
|
|
|
3,911 |
|
Net loss |
|
(25,320 |
) |
|
|
(31,782 |
) |
|
|
(112,673 |
) |
|
|
(133,204 |
) |
Other comprehensive income
(loss): |
|
|
|
|
|
|
|
Net unrealized gain (loss) on available-for-sale securities |
|
274 |
|
|
|
258 |
|
|
|
811 |
|
|
|
(753 |
) |
Net comprehensive loss |
$ |
(25,046 |
) |
|
$ |
(31,524 |
) |
|
$ |
(111,862 |
) |
|
$ |
(133,957 |
) |
Net loss per share, basic and
diluted |
$ |
(0.43 |
) |
|
$ |
(0.56 |
) |
|
$ |
(1.95 |
) |
|
$ |
(2.37 |
) |
Weighted-average number of
shares used to compute net loss per share, basic and diluted |
|
58,268 |
|
|
|
56,523 |
|
|
|
57,744 |
|
|
|
56,201 |
|
Kronos Bio, Inc.Selected Balance Sheet
Data(in thousands)(Unaudited) |
|
|
December 31, 2023 |
|
December 31, 2022 |
Cash, cash equivalents and investments |
$ |
174,986 |
|
$ |
247,947 |
Total assets |
$ |
213,279 |
|
$ |
294,938 |
Total liabilities |
$ |
54,201 |
|
$ |
50,439 |
Total stockholders’
equity |
$ |
159,078 |
|
$ |
244,499 |
|
Investor & Media Contact:Margaux
BennettVice President, Corporate Development and Investor
Relations, Kronos Bio650-781-5026mbennett@kronosbio.com
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