Allakos Provides Business Update and Reports Third Quarter 2024 Financial Results
Recent Allakos Events
- Reported safety, pharmacokinetics (PK), and pharmacodynamic (PD) results from the Phase 1 trial of subcutaneous (SC) AK006 in healthy volunteers.
- Bioavailability of subcutaneous AK006 was approximately 77%.
- Subcutaneous administered AK006 showed an estimated half-life of 12-22 days.
- Consistent with the IV formulation, skin biopsies taken from subcutaneous AK006 treated healthy volunteers showed high levels of receptor occupancy confirming AK006 reaches skin tissue mast cells.
- The 720 mg dose of AK006 showed 98% receptor occupancy at day 113 suggesting the potential for infrequent dosing.
- Single and multiple doses of IV AK006 and single dose subcutaneous AK006 up to 720 mg were well tolerated with a favorable safety profile.
- Completed enrollment of over 30 patients in the randomized, double-blind, placebo-controlled Phase 1 trial of intravenous (IV) AK006 in patients with chronic spontaneous urticaria. Data from these patients expected in early Q1 of 2025.
Upcoming Allakos Anticipated Milestones
- Report randomized double-blind, placebo-controlled data on over 30 patients from the Phase 1 trial of AK006 in patients with CSU in early Q1 of 2025.
Cash Guidance
Third Quarter 2024 Financial Results
Research and development expenses were
General and administrative expenses were
About
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
Source:
Investor Contact:
ir@allakos.com
Media Contact:
media@allakos.com
UNAUDITED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS | ||||||||||||||||
(in thousands, except per share data) | ||||||||||||||||
Three Months Ended | Nine Months Ended | |||||||||||||||
2024 | 2023 | 2024 | 2023 | |||||||||||||
Operating expenses | ||||||||||||||||
Research and development | $ | 10,874 | $ | 36,749 | $ | 65,120 | $ | 97,107 | ||||||||
General and administrative | 8,876 | 11,461 | 28,985 | 33,966 | ||||||||||||
Impairment of long-lived assets | — | — | 27,347 | — | ||||||||||||
Total operating expenses | 19,750 | 48,210 | 121,452 | 131,073 | ||||||||||||
Loss from operations | (19,750 | ) | (48,210 | ) | (121,452 | ) | (131,073 | ) | ||||||||
Interest income | 1,392 | 2,590 | 5,346 | 7,965 | ||||||||||||
Other expense, net | (14 | ) | (6 | ) | (88 | ) | (42 | ) | ||||||||
Net loss | (18,372 | ) | (45,626 | ) | (116,194 | ) | (123,150 | ) | ||||||||
Unrealized gain (loss) on investments | 325 | 87 | 284 | 212 | ||||||||||||
Comprehensive loss | $ | (18,047 | ) | $ | (45,539 | ) | $ | (115,910 | ) | $ | (122,938 | ) | ||||
Net loss per common share: | ||||||||||||||||
Basic and diluted | $ | (0.21 | ) | $ | (0.52 | ) | $ | (1.31 | ) | $ | (1.42 | ) | ||||
Weighted-average number of common shares outstanding: |
||||||||||||||||
Basic and diluted | 89,024 | 87,115 | 88,571 | 86,539 | ||||||||||||
UNAUDITED CONDENSED BALANCE SHEETS | |||||||||
(in thousands) | |||||||||
2024 | 2023 | ||||||||
Assets |
|||||||||
Current assets: | |||||||||
Cash and cash equivalents | $ | 10,449 | $ | 66,440 | |||||
Investments | 82,266 | 104,354 | |||||||
Prepaid expenses and other current assets | 4,438 | 9,095 | |||||||
Total current assets | 97,153 | 179,889 | |||||||
Property and equipment, net | 15,733 | 33,369 | |||||||
Operating lease right-of-use assets | 9,880 | 24,136 | |||||||
Other long-term assets | 1,668 | 6,216 | |||||||
Total assets | $ | 124,434 | $ | 243,610 | |||||
Liabilities and stockholders’ equity |
|||||||||
Current liabilities: | |||||||||
Accounts payable | $ | 3,964 | $ | 1,764 | |||||
Accrued expenses and other current liabilities | 12,017 | 34,814 | |||||||
Total current liabilities | 15,981 | 36,578 | |||||||
Operating lease liabilities, net of current portion | 35,710 | 38,215 | |||||||
Total liabilities | 51,691 | 74,793 | |||||||
Stockholders’ equity: | |||||||||
Common stock | 89 | 88 | |||||||
Additional paid-in capital | 1,306,991 | 1,287,156 | |||||||
Accumulated other comprehensive gain (loss) | 334 | 50 | |||||||
Accumulated deficit | (1,234,671 | ) | (1,118,477 | ) | |||||
Total stockholders’ equity | 72,743 | 168,817 | |||||||
Total liabilities and stockholders’ equity | $ | 124,434 | $ | 243,610 | |||||
Source: Allakos Inc.