Submitted New Drug Application (NDA) to the
U.S. Food and Drug Administration (FDA) for KarXT for the treatment
of schizophrenia in the third quarter of 2023
Initiated the Phase 3 ADEPT-2 and ADEPT-3
trials evaluating KarXT for the treatment of psychosis in
Alzheimer’s disease in the third quarter of 2023
$1.3 billion in cash expected to fund
operations through 2026
Conference call and webcast to take place today
at 8:00 a.m. ET
Karuna Therapeutics, Inc. (NASDAQ: KRTX), a biopharmaceutical
company driven to discover, develop, and deliver transformative
medicines for people living with psychiatric and neurological
conditions, today announced financial results for the third quarter
of 2023 and provided a general business update.
“The third quarter was highlighted by our NDA submission to the
FDA for KarXT for the treatment of schizophrenia, a significant
milestone for Karuna, as well as for patients living with this
serious mental illness,” said Bill Meury, president and chief
executive officer of Karuna Therapeutics. “There remains an unmet
need for new treatment options and, if approved, KarXT would
represent the first novel pharmacological approach to treating
schizophrenia in decades.”
“In parallel to our submission, we continue to advance our
commercialization plans ahead of the potential approval and launch
of KarXT in the U.S. in the second half of next year,” Mr. Meury
added. "Additionally, we have made important progress across our
ongoing KarXT Phase 3 programs, highlighted by the initiation of
the ADEPT-2 and ADEPT-3 trials in psychosis in Alzheimer’s disease.
Beyond our primary indications in schizophrenia and Alzheimer’s
disease, we’re also focused on building our pipeline with potential
new opportunities for KarXT, as well as advancing other early-stage
compounds across a broad range of neuropsychiatric conditions.”
KEY PIPELINE HIGHLIGHTS
Karuna is advancing a pipeline of novel drug candidates for the
treatment of various psychiatric and neurological conditions led by
KarXT (xanomeline-trospium), an oral, investigational
M1/M4-preferring muscarinic agonist.
KarXT
KarXT is being evaluated in Phase 3 clinical trials as a
potential treatment for schizophrenia, for adjunctive treatment in
schizophrenia, as well as for psychosis in Alzheimer’s disease.
- Schizophrenia
- Submitted an NDA to the FDA for KarXT for the treatment of
schizophrenia in adults in the third quarter of 2023.
- The Company anticipates the potential approval and launch of
KarXT in the second half of 2024.
- Presented additional data analyses from the EMERGENT program
at the 36th European College of Neuropsychopharmacology (ECNP)
Congress in the fourth quarter of 2023. Poster presentations
included previously reported cognition data from the EMERGENT-2 and
EMERGENT-3 trials, as well as new efficacy and safety analyses from
the EMERGENT-3 trial where:
- KarXT demonstrated a statistically significantly greater
percentage of Positive and Negative Syndrome Scale (PANSS)
responders (≥30% reduction in PANSS total score) at week 5 compared
to placebo (p<0.01), a pre-specified secondary endpoint in the
trial.
- KarXT was associated with statistically significant
improvements from baseline to week 5 compared to placebo in the
PANSS Marder 5-Factor symptom domains, including the PANSS Marder
positive (p<0.001), disorganized thoughts (p<0.05),
uncontrolled hostility/excitement (p<0.001), and
anxiety/depression (p<0.01) factors. While not meeting the
threshold for statistical significance at week 5, KarXT did
demonstrate a statistically significant reduction in the PANSS
negative Marder factor score compared to placebo at week 4
(p<0.05).
- KarXT was generally well-tolerated, with the most common
treatment emergent adverse events (TEAEs) being cholinergic in
nature, consistent with prior trials of KarXT. The majority of
these common TEAEs occurred within the first two weeks of
treatment, were mild in severity, and transient in nature.
- Additional data analyses to be presented at upcoming medical
congresses in the fourth quarter of 2023. Presentations will
highlight new pooled efficacy and safety data from the EMERGENT-1,
EMERGENT-2, and EMERGENT-3 trials.
- Topline data from the EMERGENT-4 and EMERGENT-5 trials
evaluating the long-term safety of KarXT in schizophrenia are
anticipated in the second half of 2024.
- The Company remains on track to report topline data from the
Phase 1b trial evaluating the effect of KarXT on 24-hour ambulatory
blood pressure in the fourth quarter of 2023.
- Adjunctive treatment in
schizophrenia
- Topline data from the Phase 3 ARISE trial evaluating the
efficacy and safety of KarXT in schizophrenia when combined with a
background antipsychotic is anticipated in the second half of
2024.
- Psychosis in Alzheimer’s disease
- The Phase 3 ADEPT-2 and ADEPT-3 trials initiated in the
third quarter of 2023.
- Topline data from ADEPT-1 and ADEPT-2 are anticipated in
2025.
Early-stage and discovery programs
The Karuna pipeline also includes clinical-stage candidate
KAR-2618, a TRPC4/5 inhibitor for the treatment of mood and anxiety
disorders, as well as pre-clinical muscarinic, TRPC4/5, and
target-agnostic compounds for the treatment of psychiatric and
neurological conditions.
- The Company plans to evaluate KAR-2618 for the treatment of
major depressive disorder (MDD).
- The initiation of a Phase 1b clinical trial of KAR-2618 is
anticipated in 2024, with additional details to be shared early
next year.
ANTICIPATED UPCOMING MILESTONES
- Topline data from the Phase 3 EMERGENT-4 trial (2H 2024)
- Topline data from the Phase 3 EMERGENT-5 trial (2H 2024)
- Launch of KarXT in schizophrenia, if approved (2H 2024)
- Topline data from the Phase 3 ARISE trial (2H 2024)
- Initiation of the Phase 1b trial of KAR-2618 (2024)
- Topline data from the Phase 3 ADEPT-1 trial (2025)
- Topline data from the Phase 3 ADEPT-2 trial (2025)
THIRD QUARTER 2023 FINANCIAL RESULTS
The Company reported a net loss of $119.1 million for the third
quarter of 2023, as compared to $77.0 million for the prior year
period. The increase in net loss for the quarter was driven by
research and development expenses related to the Company’s ongoing
KarXT clinical programs, pre-commercialization activities,
increased employee headcount across the organization, and higher
stock-based compensation.
Research and development expenses were $104.0 million for the
third quarter of 2023, as compared to $62.0 million for the prior
year period. The increase in research and development expenses for
the quarter was primarily driven by expenses related to the KarXT
clinical programs, increased employee headcount, and higher
stock-based compensation.
General and administrative expenses were $32.3 million for the
third quarter of 2023, as compared to $19.1 million for the prior
year period. The increase in general and administrative expenses
for the quarter was primarily driven by the Company’s
pre-commercialization activities, increased employee headcount, and
higher stock-based compensation.
The Company ended the quarter with $1.3 billion in cash, cash
equivalents, and available-for-sale investment securities compared
to $1.1 billion as of December 31, 2022. The increase was primarily
the result of the completion of the Company’s follow-on public
offering in March 2023, which resulted in net proceeds of $436.7
million. The Company expects that current cash, cash equivalents,
and available-for-sale investment securities as of September 30,
2023, will enable the Company to fund its operating expenses and
capital expenditure requirements through 2026.
CONFERENCE CALL AND WEBCAST DETAILS
The third quarter 2023 financial results and business update
will be discussed during a conference call and webcast today at
8:00 a.m. ET. A webcast of the live call may be accessed on the
Investor Relations page of Karuna’s website at
investors.karunatx.com. A replay of the webcast will be available
for up to 30 days following the event.
About Karuna Therapeutics
Karuna Therapeutics is a biopharmaceutical company driven to
discover, develop, and deliver transformative medicines for people
living with psychiatric and neurological conditions. At Karuna, we
understand there is a need for differentiated and more effective
treatments that can help patients navigate the challenges presented
by serious mental illness. Utilizing our extensive knowledge of
neuroscience, we are harnessing the untapped potential of the brain
in pursuit of novel pathways to develop medicines that make
meaningful differences in peoples’ lives. For more information,
please visit www.karunatx.com.
Forward Looking Statements
This press release contains forward looking statements within
the meaning of Section 27A of the Securities Act of 1933, as
amended, and Section 21E of the Securities Exchange Act of 1934, as
amended, including statements regarding our expectations about the
timing of our ongoing and planned clinical trials and regulatory
filings, our goals to develop and commercialize our product
candidates, our liquidity and capital resources, and other
statements identified by words such as “could,” “expects,”
“intends,” “may,” “plans,” “potential,” “should,” “will,” “would,”
or similar expressions and the negatives of those terms. Forward
looking statements are not promises or guarantees of future
performance, and are subject to a variety of risks and
uncertainties, many of which are beyond our control, and which
could cause actual results to differ materially from those
contemplated in such forward-looking statements. These factors
include risks related to our limited operating history, our ability
to obtain necessary funding, our ability to generate positive
clinical trial results for our product candidates and other risks
inherent in clinical development, the timing and scope of
regulatory approvals, changes in laws and regulations to which we
are subject, competitive pressures, our ability to identify
additional product candidates, risks relating to business
interruptions, and other risks set forth under the heading “Risk
Factors” of our Annual Report on Form 10-K for the year ended
December 31, 2022 and in our subsequent filings with the Securities
and Exchange Commission. Our actual results could differ materially
from the results described in or implied by such forward looking
statements. Forward-looking statements speak only as of the date
hereof, and, except as required by law, we undertake no obligation
to update or revise these forward-looking statements.
Karuna Therapeutics, Inc. Unaudited Consolidated
Statements of Operations (in thousands, except share and per
share data)
Three Months Ended
Nine Months Ended
September 30,
September 30,
2023
2022
2023
2022
License and other revenue
$
-
$
81
$
654
$
5,359
Operating expenses:
Research and development
103,952
61,950
281,909
158,243
General and administrative
32,266
19,125
83,936
51,756
Total operating expenses
136,218
81,075
365,845
209,999
Loss from operations
(136,218
)
(80,994
)
(365,191
)
(204,640
)
Other income, net:
Interest income
16,952
3,884
44,894
4,611
Sublease income
147
147
441
433
Total other income, net
17,099
4,031
45,335
5,044
Net loss before income taxes
(119,119
)
(76,963
)
(319,856
)
(199,596
)
Income tax provision
—
—
—
(528
)
Net loss attributable to common
stockholders
$
(119,119
)
$
(76,963
)
$
(319,856
)
$
(200,124
)
Net loss per share, basic and diluted
$
(3.16
)
$
(2.38
)
$
(8.72
)
$
(6.52
)
Weighted average common shares outstanding
used in computing net loss per share, basic and diluted
37,689,144
32,349,111
36,682,056
30,693,117
Karuna Therapeutics, Inc. Unaudited Consolidated
Balance Sheet Data (in thousands)
September 30, 2023
December 31, 2022
Cash, cash equivalents and investments
$
1,339,477
$
1,124,044
Working capital
1,316,429
1,120,823
Total assets
1,385,097
1,163,334
Total stockholders’ equity
$
1,322,316
$
1,126,238
View source
version on businesswire.com: https://www.businesswire.com/news/home/20231102261375/en/
Investors: Alexis Smith +1 (617) 352-9917
asmith@karunatx.com
Media: Julie Ciardiello +1 (917) 647-0159
julie.ciardiello@karunatx.com
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