Allakos Provides Business Update and Reports First Quarter 2024 Financial Results
09 Maio 2024 - 5:02PM
Allakos Inc. (the “Company”) (Nasdaq: ALLK), a biotechnology
company developing antibodies for the treatment of allergic,
inflammatory and proliferative diseases, today provided a business
update and reported financial results for the first quarter ended
March 31, 2024.
Recent Allakos Events
- Completed dosing in the single ascending dose (SAD) cohorts and
multiple ascending dose (MAD) cohorts of the randomized,
double-blind, placebo-controlled Phase 1 trial of Intravenous (IV)
AK006 in healthy volunteers.
- Completed dosing in the randomized, double-blind,
placebo-controlled subcutaneous (SC) AK006 cohort in healthy
volunteers.
- Initiated the randomized, double-blind, placebo-controlled
Phase 1 trial of IV AK006 in patients with chronic spontaneous
urticaria.
- Published preclinical research in Allergy showing that AK006
controls mast cell function through interaction with multiple
activating receptors and key signaling pathways.
- Presented preclinical data at the American Academy of Allergy,
Asthma & Immunology (AAAAI) Annual Meeting 2024 highlighting
AK006’s mechanism of action and ability to reduce MRGPRX2-induced
skin inflammation.
Upcoming Allakos Anticipated
Milestones
- Report safety, pharmacokinetics (PK), and pharmacodynamic (PD)
results from the Phase 1 trial of IV AK006 in healthy volunteers,
including data to confirm Siglec-6 receptor occupancy in skin
biopsy samples in Q2 2024.
- Report safety, PK, and PD results from the Phase 1 trial of SC
AK006 in healthy volunteers, including data to confirm Siglec-6
receptor occupancy in skin biopsy samples in Q3 2024.
- Report topline data from the Phase 1 trial of IV AK006 in
patients with CSU at year end 2024.
Cash Guidance
Allakos’ financial outlook, restructuring
activities and estimated cash runway as reported by the Company in
January 2024 remain unchanged. The Company reiterates that the
restructuring activities will extend the cash runway into mid-2026
and continues to expect to end 2024 with total cash, cash
equivalents and investments in the range of $81 to $86 million. The
Company reiterates that an estimated $30 million of closeout,
severance and other costs will be paid in 2024 in connection with
the lirentelimab development program. Approximately $12 million of
these payments were made in the first quarter of 2024 and the
majority of the remaining approximately $18 million is expected to
be made over the second and third quarters of 2024.
First Quarter 2024 Financial
Results
Allakos ended the first quarter of 2024 with
$139.3 million in cash, cash equivalents and investments resulting
in a net decrease in cash, cash equivalents and investments of
$31.5 million during the first quarter of 2024.
Research and development expenses were $34.8
million in the first quarter of 2024 compared to $33.1 million in
the first quarter of 2023, an increase of $1.7 million. This
quarter over quarter increase is attributed to $6.3 million of
increased manufacturing costs primarily due to lirentelimab, the
development of which was halted in January 2024, offset partially
by $2.2 million of decreased compensation costs and a $2.4 million
decrease in other research and development expenses.
General and administrative expenses were $10.9
million for the first quarter of 2024 compared to $12.0 million for
the first quarter of 2023, a decrease of $1.1 million. The quarter
over quarter change included $0.7 million of decreased compensation
costs and $0.4 million of decreased other general and
administrative expenses.
In the first quarter of 2024, Allakos recognized a
non-cash impairment charge following the significant sustained
decline observed in the Company’s market capitalization and halting
of the lirentelimab development program. The non-cash charge
totaled $27.3 million comprising of the write-down of long-term
assets associated with our office lease and related assets to
estimated fair market value.
Allakos reported a net loss of $71.1 million in
the first quarter of 2024 compared to $42.4 million in the first
quarter of 2023. Net loss per basic and diluted share was $0.81 for
the first quarter of 2024 compared to $0.49 in the first quarter of
2023.
About Allakos
Allakos is a clinical stage biotechnology company
developing therapeutics that target immunomodulatory receptors
present on immune effector cells involved in allergy, inflammatory
and proliferative diseases. Activating these immunomodulatory
receptors allows for the direct targeting of cells involved in
disease pathogenesis and, in the setting of allergy and
inflammation, has the potential to result in broad inhibition of
inflammatory cells. The Company’s most advanced product candidate
is AK006. AK006 targets Siglec-6, an inhibitory receptor expressed
on mast cells. Mast cells are widely distributed in the body and
play a central role in the inflammatory response. Inappropriately
activated mast cells have been identified as key drivers in a
number of severe diseases affecting the gastrointestinal tract,
eyes, skin, lungs and other organs. In preclinical studies, AK006
appears to provide deep mast cell inhibition and, in addition to
its inhibitory activity, reduce mast cell numbers. For more
information, please visit the Company’s website at
www.allakos.com.
Forward-Looking Statements
This press release contains forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995 as contained in Section 27A of the Securities
Act of 1933, as amended, and Section 21E of the Securities Exchange
Act of 1934, as amended. Such forward-looking statements include,
but are not limited to, Allakos’ expected timing of reporting data
from its clinical trial of AK006; cash guidance and runway; and
restructuring. Such statements are subject to numerous important
factors, risks and uncertainties that may cause actual events or
results to differ materially from current expectations and beliefs,
including but not limited to: Allakos’ stages of clinical drug
development; Allakos’ ability to timely initiate and complete
clinical trials for AK006; Allakos’ ability to obtain required
regulatory approvals for its clinical trials; uncertainties related
to the enrollment of patients in its clinical trials; Allakos’
ability to demonstrate sufficient safety and efficacy of its
product candidates in its clinical trials; uncertainties related to
the success of clinical trials, regardless of the outcomes of
preclinical testing or early-stage trials; Allakos’ ability to
obtain regulatory approvals to market its product candidates;
market acceptance of Allakos’ product candidates; uncertainties
related to the projections of the size of patient populations
suffering from the diseases Allakos is targeting; Allakos’ ability
to advance additional product candidates beyond AK006;
uncertainties related to Allakos’ ability to realize the
contemplated benefits of its restructuring and related reduction in
force; Allakos’ ability to accurately forecast financial results;
Allakos’ ability to obtain additional capital to finance its
operations, research and drug development; general economic and
market conditions, both domestic and international; domestic and
international regulatory obligations; and other risks. Information
regarding the foregoing and additional risks may be found in the
section entitled “Risk Factors” in documents that Allakos files
from time to time to with the SEC. These documents contain and
identify important factors that could cause the actual results for
Allakos to differ materially from those contained in Allakos’
forward-looking statements. Any forward-looking statements
contained in this press release speak only as of the date hereof,
and Allakos specifically disclaims any obligation to update any
forward-looking statement, except as required by law. These
forward-looking statements should not be relied upon as
representing Allakos’ views as of any date subsequent to the date
of this press release.
Source: Allakos Inc.
Investor Contact: Adam Tomasi, President Alex
Schwartz, VP Strategic Finance and Investor Relations
ir@allakos.com
Media Contact: Denise Powell
denise@redhousecomms.com
|
ALLAKOS
INC.UNAUDITED STATEMENTS OF OPERATIONS AND
COMPREHENSIVE LOSS (in thousands, except per share
data) |
|
|
|
Three Months
Ended |
|
|
|
March 31, |
|
|
|
2024 |
|
|
2023 |
|
Operating expenses |
|
|
|
|
|
|
Research and development |
|
$ |
34,824 |
|
|
$ |
33,078 |
|
General and administrative |
|
|
10,898 |
|
|
|
11,968 |
|
Impairment of long-lived assets |
|
|
27,347 |
|
|
|
— |
|
Total operating expenses |
|
|
73,069 |
|
|
|
45,046 |
|
Loss from operations |
|
|
(73,069 |
) |
|
|
(45,046 |
) |
Interest income |
|
|
1,995 |
|
|
|
2,678 |
|
Other expense, net |
|
|
(72 |
) |
|
|
(36 |
) |
Net loss |
|
|
(71,146 |
) |
|
|
(42,404 |
) |
Unrealized gain (loss) on investments |
|
|
(30 |
) |
|
|
296 |
|
Comprehensive loss |
|
$ |
(71,176 |
) |
|
$ |
(42,108 |
) |
Net loss per common share: |
|
|
|
|
|
|
Basic and diluted |
|
$ |
(0.81 |
) |
|
$ |
(0.49 |
) |
Weighted-average number of common shares outstanding: |
|
|
|
|
|
|
Basic and diluted |
|
|
88,042 |
|
|
|
85,845 |
|
|
ALLAKOS
INC.UNAUDITED CONDENSED BALANCE SHEETS
(in thousands) |
|
|
|
March
31, |
|
|
December
31, |
|
|
|
2024 |
|
|
2023 |
|
Assets |
|
|
|
|
|
|
Current assets: |
|
|
|
|
|
|
Cash and cash equivalents |
|
$ |
43,060 |
|
|
$ |
66,440 |
|
Investments |
|
|
96,192 |
|
|
|
104,354 |
|
Prepaid expenses and other current assets |
|
|
8,382 |
|
|
|
9,095 |
|
Total current assets |
|
|
147,634 |
|
|
|
179,889 |
|
Property and equipment, net |
|
|
17,364 |
|
|
|
33,369 |
|
Operating lease right-of-use assets |
|
|
10,577 |
|
|
|
24,136 |
|
Other long-term assets |
|
|
1,737 |
|
|
|
6,216 |
|
Total assets |
|
$ |
177,312 |
|
|
$ |
243,610 |
|
Liabilities and stockholders’ equity |
|
|
|
|
|
|
Current liabilities: |
|
|
|
|
|
|
Accounts payable |
|
$ |
15,748 |
|
|
$ |
1,764 |
|
Accrued expenses and other current liabilities |
|
|
20,173 |
|
|
|
34,814 |
|
Total current liabilities |
|
|
35,921 |
|
|
|
36,578 |
|
Operating lease liabilities, net of current portion |
|
|
37,408 |
|
|
|
38,215 |
|
Total liabilities |
|
|
73,329 |
|
|
|
74,793 |
|
Stockholders’ equity: |
|
|
|
|
|
|
Common stock |
|
|
89 |
|
|
|
88 |
|
Additional paid-in capital |
|
|
1,293,497 |
|
|
|
1,287,156 |
|
Accumulated other comprehensive gain (loss) |
|
|
20 |
|
|
|
50 |
|
Accumulated deficit |
|
|
(1,189,623 |
) |
|
|
(1,118,477 |
) |
Total stockholders’ equity |
|
|
103,983 |
|
|
|
168,817 |
|
Total liabilities and stockholders’ equity |
|
$ |
177,312 |
|
|
$ |
243,610 |
|
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