Allakos Reports Fourth Quarter and Full Year 2018 Financial Results and 2018 Corporate Highlights
Key Accomplishments in 2018
- Orphan drug designation granted in
February 2018by U.S. Food and Drug Administration( FDA) for the treatment of Eosinophilic Gastritis (EG) and Eosinophilic Gastroenteritis (EGE) with AK002.
- Initiated a placebo-controlled double-blind Phase 2 study in patients with EG and/or EGE. Topline results from the study are expected mid-2019.
- Initiated and completed an open-label Phase 2 study in patients with Chronic Urticaria (CU). Topline results from the study were reported in the first quarter of 2019.
- Completed an open-label Phase 1 study in patients with Indolent Systemic Mastocytosis (ISM). Topline results from the study were reported in the first quarter of 2019.
- Initiated an open-label Phase 1 study in patients with Severe Allergic Conjunctivitis (SAC). Topline results from the study are expected in the first or second quarter of 2019.
- Closed an initial public offering (IPO) and concurrent private placement in
July 2018, issuing 8,453,332 shares of common stock at an offering price of $18.00per share. Aggregate cash proceeds received from the IPO and concurrent private placement were approximately $138.4 million, net of underwriting discounts, commissions and offering expenses.
Fourth Quarter and Full Year 2018 Financial Results
Research and development expenses were $11.0 million in the fourth quarter of 2018 as compared to $5.1 million in the same period in 2017, an increase of
General and administrative expenses were $4.5 million in the fourth quarter of 2018 as compared to $1.4 million in the same period in 2017, an increase of
Allakos is a clinical stage biotechnology company developing antibodies that target immunomodulatory receptors present on immune effector cells involved in allergic, inflammatory, and proliferative diseases. The Company’s lead antibody, AK002, targets Siglec-8, an inhibitory receptor selectively expressed on human mast cells and eosinophils. Inappropriately activated eosinophils and mast cells have been identified as key drivers in a number of severe diseases affecting the gastrointestinal tract, eyes, skin, lungs and other organs. AK002 has completed Phase 1 studies in healthy volunteers, indolent systemic mastocytosis, and a Phase 2 trial in patients with chronic urticaria. AK002 demonstrated pharmacodynamic activity in trials and in the trials involving patients with chronic urticaria and indolent systemic mastocytosis, patients reported improvements in their symptoms. AK002 is being tested in a double-blind, placebo-controlled Phase 2 trial for the treatment of eosinophilic gastritis and eosinophilic gastroenteritis. In addition, Allakos is conducting multiple-dose trials with AK002 in severe allergic conjunctivitis. For more information, please visit the Company's website at www.allakos.com.
This press release contains forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Such forward-looking statements include, but are not limited to, the timing of top-line results from Allakos’ ongoing clinical trials. 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’ early stages of clinical drug development; Allakos’ ability to timely complete clinical trials for, and if approved, commercialize AK002, its lead compound; Allakos’ ability to obtain required regulatory approvals for its product candidates; 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 later-stage clinical trials, regardless of the outcomes of preclinical testing and early-stage trials; market acceptance of Allakos’ product candidates; uncertainties related to the projections of the size of patient populations suffering from the diseases
|Investor Contact:||Media Contact:|
|Adam Tomasi, COO, CFO||Denise Powell|
|STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS|
|(in thousands, except per share data)|
|Three Months Ended||Year Ended|
|December 31,||December 31,|
|Research and development||$ 11,031||$ 5,051||$ 33,287||$ 18,506|
|General and administrative||4,482||1,395||12,434||3,748|
|Total operating expenses||15,513||6,446||45,721||22,254|
|Loss from operations||(15,513||)||(6,446||)||(45,721||)||(22,254||)|
|Interest income (expense), net||1,023||(586||)||2,375||(1,302||)|
|Other expense, net||(38||)||(177||)||(192||)||(287||)|
|Loss before benefit from income taxes||(14,528||)||(7,209||)||(43,538||)||(23,843||)|
|Provision for (benefit from) income taxes||—||675||—||(291||)|
|Unrealized loss on marketable securities, net of
|Comprehensive loss||$ (14,510||)||$ (7,884||)||$ (43,553||)||$ (23,552||)|
|Net loss per common share:|
|Basic and diluted||$ (0.35||)||$ (4.08||)||$ (2.20||)||$ (14.54||)|
|Weighted-average number of common shares
|Basic and diluted||42,068||1,930||19,833||1,620|
|CONDENSED BALANCE SHEETS|
|Cash and cash equivalents||$ 33,660||$ 85,207|
|Investments in marketable securities||145,246||—|
|Prepaid expenses and other current assets||2,703||1,037|
|Total current assets||181,609||86,244|
|Property and equipment, net||8,848||445|
|Other long-term assets||802||340|
|Total assets||$ 191,259||$ 87,029|
|Liabilities, convertible preferred stock and stockholders' equity (deficit)|
|Accounts payable||$ 2,092||$ 1,703|
|Accrued expenses and other current liabilities||3,164||1,089|
|Total current liabilities||5,256||2,792|
|Other long-term liabilities||2,009||36|
|Convertible preferred stock||—||142,969|
|Stockholders' equity (deficit):|
|Additional paid-in capital||288,079||1,803|
|Accumulated other comprehensive income||(15||)||—|
|Total stockholders’ equity (deficit)||183,994||(58,768||)|
|Total liabilities, convertible preferred stock and stockholders’ equity (deficit)||$ 191,259||$ 87,029|
Source: Allakos Inc.