ASLAN Pharmaceuticals Reports First Quarter 2019 Financial Results and Provides Corporate Update
Dr
First quarter 2019 and recent business highlights
Clinical development
Varlitinib
- The varlitinib global pivotal TreeTopp (TREatmEnT OPPortunity) study completed patient enrolment ahead of schedule with the recruitment of 127 patients with biliary tract cancer (BTC) who failed first line therapy from 56 sites worldwide including the US,
Europe ,Australia ,Japan ,Korea , and otherAsia Pacific countries. The trial is ongoing and proceeding according to plan. - In January, positive varlitinib data was presented in first-line biliary tract cancer in combination with chemotherapy at the
American Society of Clinical Oncology Gastrointestinal Cancers Symposium (ASCO GI). The data demonstrated a response rate of 44% across all evaluable patients and a 60% response rate in the highest dose cohort, compared to historical rates of 26% with current standard of care treatment.
ASLAN003
- Completed the third cohort (100mg BID) in phase 2a trial testing ASLAN003 in acute myeloid leukemia (AML). Six patients recruited into the fourth cohort (200mg BID). All patients are currently ongoing.
ASLAN004
- Completed the first part of the phase 1 single ascending dose (SAD) study testing the intravenous formulation of the first-in-class therapeutic antibody ASLAN004 in healthy volunteers. ASLAN004 is a fully human monoclonal antibody that binds to the IL-13 receptor α1 subunit (IL-13Rα1), blocking signalling of two pro-inflammatory cytokines, IL-4 and IL-13, which are central to triggering symptoms of atopic dermatitis, such as redness and itching of the skin. Analysis of downstream mediators demonstrated complete inhibition within one hour of dosing, which was then maintained for more than 29 days, suggesting monthly dosing may be achievable.
- Last patient dosed in the second part of the ongoing SAD trial on 27 March. ASLAN is testing a subcutaneous formulation and expects to report data from this part of the study in May. Initiation of a multiple ascending dose study in patients with moderate to severe atopic dermatitis is planned for the second half of 2019.
Corporate updates
- In February, ASLAN entered into an agreement with
BioGenetics Co Ltd that granted exclusive commercialisation rights for varlitinib in all indications inSouth Korea . ASLAN received an upfront payment ofUS$2 million and can receive up toUS$11 million in sales and development milestones. ASLAN is also eligible to receive tiered royalties on net sales from the high-teens to the mid-twenties range. - In March, ASLAN entered into a second agreement with
BioGenetics Co Ltd that granted exclusive commercialisation rights for ASLAN003 in all indications inSouth Korea . Under terms of the agreement, ASLAN received an upfront payment ofUS$1 million and is eligible to receive up toUS$8 million in sales and development milestones. ASLAN is also eligible to receive tiered royalties on net sales from the high-teens to the mid-twenties range.
Anticipated upcoming milestones
- Topline global pivotal trial (TreeTopp) data on varlitinib as second line treatment for biliary tract cancer in the second half of 2019.
- Part 1 readout of ASLAN003 phase 2 trial in the second quarter of 2019.
- Completion of single ascending dose trial for ASLAN004 in atopic dermatitis in the second quarter of 2019.
- Initiation of a multiple ascending dose trial for ASLAN004 in patients with moderate to severe atopic dermatitis in the second half of 2019.
First quarter 2019 financial results
- Cash used in operations for the quarter ended
31 March 2019 wasUS$7.2 million compared toUS$10.0 million in the same period in 2018. - Research and development (R&D) expense was
US$4.4 million and general and administrative (G&A) expense wasUS$2.3 million for the first quarter of 2019, compared toUS$5.6 million andUS$2.8 million , respectively, in the same period in 2018. The decrease in R&D expense was due to the completion of clinical studies and lower manufacturing expenses. The decrease in G&A expense was the result of the restructuring implemented inJanuary 2019 . - Net loss for the first quarter of 2019 was
US$4.3 million compared to a net loss ofUS$8.7 million for the first quarter of 2018. The narrower loss in the first quarter of 2019 was due primarily to recognition of theUS$3 million upfront payment from the licensing agreements withBioGenetics Co Ltd and lower operational costs. - Cash, cash equivalents and short-term investments totaled
US$21.6 million as of31 March 2019 compared toUS$28.9 million as of31 December 2018 . Weighted average shares outstanding for the first quarter of 2019 was 160.2 million compared to 130.2 million for the first quarter of 2018. One American Depositary Share is the equivalent of five ordinary shares.
Consolidated Balance Sheet1
(in US dollars, unaudited)
March 31, 2019 (Reviewed) |
December 31, 2018 (Audited) |
||||||||||
ASSETS | Amount | Amount | |||||||||
CURRENT ASSETS | |||||||||||
Cash and cash equivalents | $ | 21,620,307 | $ | 28,908,901 | |||||||
Accounts receivable | 1,000,000 | - | |||||||||
Prepayments | 248,300 | 183,599 | |||||||||
Total current assets | 22,868,607 | 29,092,500 | |||||||||
NON-CURRENT ASSETS | |||||||||||
Financial assets at fair value through profit or loss | 60,004 | 60,004 | |||||||||
Financial assets at fair value through other comprehensive income | 187,244 | 187,244 | |||||||||
Property, plant and equipment | 226,149 | 288,418 | |||||||||
Right-of-use assets | 267,111 | - | |||||||||
Intangible assets | 23,079,180 | 23,080,592 | |||||||||
Refundable deposits | 174,206 | 172,080 | |||||||||
Total non-current assets | 23,993,894 | 23,788,338 | |||||||||
TOTAL | $ | 46,862,501 | $ | 52,880,838 | |||||||
LIABILITIES AND EQUITY | |||||||||||
CURRENT LIABILITIES | |||||||||||
Trade payables | $ | 3,706,431 | $ | 5,315,737 | |||||||
Other payables | 2,094,057 | 2,682,661 | |||||||||
Lease liabilities - current | 223,833 | - | |||||||||
Total current liabilities | 6,024,321 | 7,998,398 | |||||||||
NON-CURRENT LIABILITIES | |||||||||||
Long-term borrowings | 14,139,819 | 13,974,794 | |||||||||
Lease liabilities - non-current | 42,238 | - | |||||||||
Other non-current liabilities | 365,230 | 289,613 | |||||||||
Total non-current liabilities | 14,547,287 | 14,264,407 | |||||||||
Total liabilities | 20,571,608 | 22,262,805 | |||||||||
EQUITY | |||||||||||
Ordinary shares | 51,627,219 | 51,627,219 | |||||||||
Capital surplus | 111,476,574 | 111,459,672 | |||||||||
Accumulated deficits | (136,812,900 | ) | (132,468,858 | ) | |||||||
Total equity | 26,290,893 | 30,618,033 | |||||||||
TOTAL | $ | 46,862,501 | $ | 52,880,838 | |||||||
Consolidated Statements of Comprehensive Income1
(in US dollars, unaudited)
For the Three Months Ended March 31 | |||||||||||||
2019 | 2018 | ||||||||||||
Amount |
Amount | ||||||||||||
SALES | $ | 3,000,000 | $ | - | |||||||||
OPERATING COSTS | 100,000 | - | |||||||||||
GROSS PROFIT | 2,900,000 | - | |||||||||||
OPERATING EXPENSES | |||||||||||||
General and administrative | (2,256,361 | ) | (2,807,871 | ) | |||||||||
Research and development | (4,449,532 | ) | (5,622,802 | ) | |||||||||
Total operating expenses | (6,705,893 | ) | (8,430,673 | ) | |||||||||
LOSS FROM OPERATIONS | (3,805,893 | ) | (8,430,673 | ) | |||||||||
NON-OPERATING INCOME AND EXPENSES | |||||||||||||
Interest income | 69,024 | 61,546 | |||||||||||
Other gains and losses | (404,555 | ) | (262,426 | ) | |||||||||
Finance costs | (199,700 | ) | (112,275 | ) | |||||||||
Total non-operating income and expenses | (535,231 | ) | (313,155 | ) | |||||||||
LOSS BEFORE INCOME TAX | (4,341,124 | ) | (8,743,828 | ) | |||||||||
INCOME TAX EXPENSE | (2,918 | ) | - | ||||||||||
NET LOSS FOR THE PERIOD | (4,344,042 | ) | (8,743,828 | ) | |||||||||
TOTAL COMPREHENSIVE LOSS FOR THE PERIOD | $ | (4,344,042 | ) | $ | (8,743,828 | ) | |||||||
LOSS PER SHARE | |||||||||||||
Basic | $ | (0.03 | ) | $ | (0.07 | ) | |||||||
Avg. Shares Outstanding | 160,248,940 | 130,128,940 |
1 Financial statements in US dollars are prepared by the Company
Media and IR contacts
Emma Thompson Spurwing Communications Tel: +65 6751 2021 Email: ASLAN@spurwingcomms.com |
Robert Uhl Westwicke Partners Tel: +1 858 356 5932 Email: robert.uhl@westwicke.com |
About
Forward looking statements
This release and the accompanying financial information, contain forward-looking statements. These statements are based on the current beliefs and expectations of the management of ASLAN Pharmaceuticals Limited and/or its affiliates (the "Company"). These forward-looking statements may include, but are not limited to, statements regarding the Company’s business strategy, the Company’s plans to develop and commercialise its product candidates, the safety and efficacy of the Company’s product candidates, the Company’s plans and expected timing with respect to regulatory filings and approvals, and the size and growth potential of the markets for the Company’s product candidates. The Company’s estimates, projections and other forward-looking statements are based on management's current assumptions and expectations of future events and trends, which affect or may affect the Company’s business, strategy, operations or financial performance, and inherently involve significant known and unknown risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation the risk factors described in the Company’s US Securities and Exchange Commission filings and reports (Commission File No. 001-38475), including the Company’s prospectus dated May 8, 2018 filed with the US Securities and Exchange Commission on such date.
All statements other than statements of historical fact are forward-looking statements. The words “believe,” “may,” “might,” “could,” “will,” “aim,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “plan,” or the negative of those terms, and similar expressions that convey uncertainty of future events or outcomes are intended to identify estimates, projections and other forward-looking statements. Estimates, projections and other forward-looking statements speak only as of the date they were made, and, except to the extent required by law, the Company undertakes no obligation to update or review any estimate, projection or forward-looking statement.
Source: ASLAN Pharmaceuticals Limited