ASLAN Pharmaceuticals Reports Third Quarter 2022 Financial Results and Provides Corporate Update

  • Company maintains healthy operating position with US$68.9 million in cash, cash equivalents and short-term investments as of September 30, 2022; expected runway through late 2023
  • New TREK-DX clinical program studying eblasakimab’s potential in dupilumab experienced atopic dermatitis (AD) patients on track to enroll first patient by the end of 2022
  • The Phase 2b TREK-AD trial for eblasakimab in biologic naïve moderate-to-severe AD patients is on track and anticipated to generate topline data in Q2 2023

SAN MATEO, Calif. and SINGAPORE, Oct. 28, 2022 (GLOBE NEWSWIRE) -- ASLAN Pharmaceuticals (Nasdaq: ASLN), a clinical-stage, immunology-focused biopharmaceutical company developing innovative treatments to transform the lives of patients, today announced financial results for the third quarter ended September 30, 2022, and provided an update on recent corporate activities.

“In the third quarter we presented a number of new and important insights on eblasakimab’s differentiated mechanism of action in neuronal itch and inflammatory pathways, and the potential improvements for AD patients related to itch and sleep loss, which are often the most burdensome symptoms reported by these patients,” shared Dr Carl Firth, CEO, ASLAN Pharmaceuticals. “We look forward to the topline readout of Phase 2b data evaluating eblasakimab in biologic naïve moderate-to-severe AD patients in Q2 2023. In the lead up to the new data that we will generate from both TREK-AD and TREK-DX, we are building a robust set of insights from ongoing research collaborations that will be presented early next year, to support eblasakimab's potential as a differentiated treatment for moderate-to-severe AD with broad therapeutic potential in Type 2-driven inflammatory diseases.”

Third quarter 2022 and recent business highlights


  • In August, the Company signed a licensing agreement with for the use of belleStudy™ digital image capture software across several global sites in the ongoing TREK-AD study of eblasakimab in AD. The easy-to-use solution enables standardized recording of AD disease severity scores through image capture and the technology will allow ASLAN to further enhance its quality control procedures in the TREK-AD study.
  • In September, three posters with new data on biomarkers, efficacy measures and patient reported outcome measures from the previously reported Phase 1b proof-of-concept trial of eblasakimab were presented at the 31st European Academy of Dermatology and Venereology (EADV) annual congress. The data showed eblasakimab suppresses downstream inflammatory biomarkers of AD, and this effect continues four to six weeks after the last dose administered. Patients treated with eblasakimab demonstrated notable improvements in quality-of-sleep measures and eblasakimab was shown to reduce P-NRS (itch) scores versus placebo, with improvements throughout the eight-week course of treatment across all dose cohorts. The posters can be found in the News and Publications section of the Company’s website.
  • In September, the Company commenced TREK-DX (TRials in EblasaKimab in Dupilumab eXperienced AD patients), a new clinical trial studying eblasakimab in dupilumab-experienced moderate-to-severe AD patients. The trial consists of a 16-week treatment period and a 12-week safety follow-up period. The primary efficacy endpoint is percentage change in Eczema Area Severity Index (EASI) score from baseline to week 16. In combination with the data from biologic naïve AD patients in the TREK-AD trial, we believe the results from the TREK-DX study in the biologic-experienced population could position eblasakimab as a preferred first choice treatment for moderate-to-severe AD.
  • The Company hosted a Research and Development Day in September where management gave a comprehensive update on the eblasakimab development program. Dr Peter A Lio, from Northwestern University Feinberg School of Medicine, and Dr Shawn Kwatra, from Johns Hopkins University, discussed the emerging unmet needs, therapeutic landscape and underlying molecular mechanisms in AD and Type 2-driven diseases. A replay of the event and presentation materials can be found in the Investor Relations section of the Company’s website.
  • In September, the Company presented new translational data on eblasakimab at the late-breaker session of the European Society for Dermatological Research (ESDR) annual meeting. The first data from the ongoing collaboration with Dr Shawn Kwatra and Dr Madan Kwatra showed increased IL-13Rα1 expression on mast cells and eosinophils in skin samples from AD patients, reinforcing the central role of IL-13Rα1 in AD. In human neuron models, eblasakimab significantly reduced neuronal itch sensitization caused by distinct IL-4 and IL-13 itch pathways and an emerging role of IL-13Rα1 signaling in mediating neuronal excitability and sensitivity beyond AD was also identified.

Farudodstat (ASLAN003)

  • A clinical development plan in skin autoimmune diseases is being finalized and a Phase 2 trial is expected to commence in the first half of 2023. 

Anticipated upcoming milestones

  • First patient enrolled in the TREK-DX trial by the end of 2022.
  • New translational data highlighting the unique effects of eblasakimab’s mechanism of action will be presented in early 2023.
  • Topline data from the Phase 2b TREK-AD trial of eblasakimab is expected in Q2 2023.

Third quarter 2022 financial highlights

  • Cash used in operating activities for the third quarter of 2022 was US$9.1 million compared to US$7.6 million in the same period in 2021.
  • Cash, cash equivalents and short-term investments as of September 30, 2022, were US$68.9 million.
  • Research and development expenses were US$8.0 million in the third quarter of 2022 compared to US$5.3 million in the third quarter of 2021. The increase was due to clinical development and manufacturing costs for eblasakimab.
  • General and administrative expenses were US$2.3 million in the third quarter of 2022 compared to US$2.8 million in the third quarter of 2021.
  • Net loss attributable to stockholders for the third quarter of 2022 was US$10.9 million compared to a net loss of US$8.6 million for the third quarter of 2021.
  • The weighted average number of American Depositary Shares (ADS) outstanding in the computation of basic loss per share for the third quarter of 2022 was 69.7 million (representing 348.7 million ordinary shares), the same as the third quarter of 2021. One ADS is the equivalent of five ordinary shares.

ASLAN Pharmaceuticals Limited
(In US Dollars)

   December 31, 2021
   September 30, 2022
Cash and cash equivalents $90,167,967  $57,752,827 
Short-term investments  -   11,196,343 
Total cash, cash equivalents, and short-term investments  90,167,967   68,949,170 
Other assets  3,612,846   3,225,270 
Total current assets $93,780,813  $72,174,440 
Investment in associate company  494,728   54,102 
Property, plant and equipment  34,979   44,064 
Right-of-use assets  197,746   332,803 
Intangible assets  9,956   6,866 
Total non-current assets  737,409   437,835 
TOTAL ASSETS $94,518,222  $72,612,275 
Trade payables $3,116,786  $11,043,988 
Other payables  2,817,909   2,724,539 
Lease liabilities - current  199,124   282,737 
Financial liabilities at fair value through profit or loss  223,352   143,712 
Total current liabilities  6,357,171   14,194,976 
Long-term borrowings  30,857,308   36,352,304 
Total non-current liabilities  30,857,308   36,352,304 
Total liabilities  37,214,479   50,547,280 
Ordinary shares  63,019,962   63,019,962 
Capital surplus  221,467,061   223,129,687 
Accumulated deficits  (227,004,332)  (263,905,706)
Other reserves  (178,948)  (178,948)
Total equity attributable to stockholders of the Company  57,303,743   22,064,995 
Total equity  57,303,743   22,064,995 
TOTAL LIABILITIES AND EQUITY $94,518,222  $72,612,275 

ASLAN Pharmaceuticals Limited
(In US Dollars, other than shares or share data)

 For the Three Months Ended
September 30

For the Nine Months Ended
September 30
 2021  2022  2021  2022 
General and administrative expenses$(2,768,498) $(2,318,889) $(9,653,235) $(7,173,938)
Research and development expenses (5,261,740)  (7,975,962)  (13,057,003)  (27,315,008)
Total operating expenses (8,030,238)  (10,294,851)  (22,710,238)  (34,488,946)





Other income 4,271   66,677   335,959   223,427 
Interest income 20   86,642   177   130,439 
Other gains and losses 103,130   246,923   1,250,241   541,496 
Finance costs (498,150)  (937,111)  (1,113,052)  (2,897,432)
Total non-operating income and expenses (390,729)  (536,869)  473,325   (2,002,070)
Share in losses of associated company, accounted for using equity method (133,523)  (78,144)  (215,403)  (390,516)
LOSS BEFORE INCOME TAX (8,554,490)  (10,909,864)  (22,452,316)  (36,881,532)
INCOME TAX EXPENSE -   (19,842)  -   (19,842)
NET LOSS FOR THE PERIOD (8,554,490)  (10,929,706)  (22,452,316)  (36,901,374)










Stockholders of the Company$(8,554,490) $(10,929,706) $(22,452,316) $(36,901,374)
 $(8,554,490) $(10,929,706) $(22,452,316) $(36,901,374)
Stockholders of the Company$(8,554,490) $(10,929,706) $(22,452,316) $(36,901,374)
 $(8,554,490) $(10,929,706) $(22,452,316) $(36,901,374)

Basic and diluted$(0.02) $(0.03) $(0.07) $(0.11)
Basic and diluted$(0.12) $(0.16) $(0.35) $(0.53)
Weighted-average number of ordinary shares in the computation of basic loss per ordinary share 

Weighted-average number of ADS in the computation of basic loss per ADS

Each ADS represents five ordinary shares

About ASLAN Pharmaceuticals

ASLAN Pharmaceuticals (Nasdaq: ASLN) is a clinical-stage, immunology-focused biopharmaceutical company developing innovative treatments to transform the lives of patients. ASLAN is currently evaluating eblasakimab, a potential first-in-class antibody targeting the IL-13 receptor, in atopic dermatitis, and farudodstat, a potent oral inhibitor of the enzyme DHODH, in autoimmune disease. ASLAN has a team in California and in Singapore. For additional information please visit or follow ASLAN on LinkedIn.

Forward-looking statements

This release contains 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 and clinical development plans; the Company’s plans to develop and commercialize eblasakimab and farudodstat; the safety and efficacy of eblasakimab and farudodstat; the Company’s plans and expected timing with respect to clinical trials, clinical trial enrollment and clinical trial results for eblasakimab and farudodstat; the potential of eblasakimab as a first-in-class treatment for atopic dermatitis and of farudodstat as a treatment for autoimmune disease; and the Company’s cash runway. 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 many risks and uncertainties, which include, unexpected safety or efficacy data observed during preclinical or clinical studies; clinical site activation rates or clinical trial enrollment rates that are lower than expected; the impact of the COVID-19 pandemic or the ongoing conflict between Ukraine and Russia on the Company’s business and the global economy; general market conditions; changes in the competitive landscape; and the Company’s ability to obtain sufficient financing to fund its strategic and clinical development plans. Other factors that may cause actual results to differ from those expressed or implied in such forward-looking statements are described in the Company’s US Securities and Exchange Commission filings and reports (Commission File No. 001-38475), including the Company’s Annual Report on Form 20-F filed with the US Securities and Exchange Commission on March 25, 2022. 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.

Media and IR contacts

Emma Thompson
Spurwing Communications
Tel: +65 6206 7350
Ashley R. Robinson
LifeSci Advisors, LLC
Tel: +1 (617) 430-7577

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