TLC Reports Second Quarter 2020 Financial Results and Provides Business Update
“I am happy to report that we have recently reached the halfway mark in patient enrollment in our EXCELLENCE trial and are on schedule to complete enrollment by the end of this year,” commented
Clinical Pipeline Update and Upcoming Milestones
- 50% enrollment complete in EXCELLENCE for TLC599. The Phase III, multi-center, randomized, double-blind, placebo- and active comparator- controlled pivotal study evaluating the efficacy and safety of both a single and a repeated dose of TLC599 for symptomatic knee osteoarthritis has enrolled half of all 500 patients. Some patients have proceeded to receive a second injection at week 24. EXCELLENCE remains on-track to complete enrollment before the end of 2020, with topline data expected in late 2021.
- Subgroup analyses of TLC599 Phase II data confirm robustness of response through 24 weeks. The pattern of responsiveness seen in the overall population, with greater reductions in pain by TLC599 than with placebo, sustaining from Week 1 to Week 24, was remarkably consistent between the subgroups, which were categorized based on gender, age, Kellgren-Lawrence grade, unilateral or bilateral knee pain, baseline Visual Analog scale pain scores and baseline
Western Ontario and McMaster Universities Index (WOMAC) pain scores. These findings were accepted as an abstract atOsteoarthritis Research Society International (OARSI) 2020 and published in the Osteoarthritis and Cartilage journal (#722).
- Positive results for TLC590 Phase II trial for postsurgical pain following bunionectomy. In this randomized, double-blind, placebo- and comparator-controlled study of 150 patients, TLC590 demonstrated greater reductions in pain than both placebo and bupivacaine through 168 hours. TLC590 achieved statistically significant pain relief over placebo and bupivacaine from 0-12, 0-24, 0-36 and 0-48 hours as measured by area under the curve on the numerical pain rating scale. TLC590 significantly delayed the time to first opioid use; total opioid consumption of TLC590 was less than placebo and bupivacaine at every time point through 168 hours. TLC590 was well-tolerated, with a safety profile comparable to bupivacaine and placebo.
- Introduction of inhalable liposomal hydroxychloroquine (HCQ) to potentially treat COVID-19. A manuscript pre-print that has been made publicly available found that TLC’s sustained release, liposomal formulation of HCQ, with targeted delivery of a tiny but therapeutic dose directly to the lung, can dramatically reduce systemic and cardiac adverse events, which was cause for termination in several global clinical trials involving orally administered – and extremely high doses – of HCQ.
Corporate Highlights
- Completed
US$23 million financing along with aUS$12 million venture financing fromCathay Bank , which, along with existing cash and equivalents, we expect will provide sufficient funding for operations into EXCELLENCE’s data readout.
- Scheduled to present at several conferences in September.
TLC will be virtually attending and presenting at Baird’s 2020Virtual Global Healthcare Conference (September 9-10 ), HC Wainwright 22nd AnnualGlobal Investment Conference (September 14-16 ),Cantor Virtual Global Healthcare Conference (September 15-17 ) and Oppenheimer Fall Healthcare Life Sciences & MedTech Summit (September 21-23 ). Details on presentations times will follow closer to the dates.
- Ampholipad™ receives approval for scale-up production. Production of TLC’s AmBisome® generic can now exceed a million vials a year, a capacity capable of meeting global demands.
- Expanded global intellectual property protection to 234 patents spanning 41 countries/territories, with 149 patents granted and 85 applications worldwide as of
June 30, 2020 .
Financial Results
Operating revenue for the second quarter of fiscal 2020 was
The Company’s cash and cash equivalents were
Financial Summary
Selected Consolidated Balance Sheet Data
Cash and cash equivalents | $ | 1,023,874 | $ | 34,232 | $ | 1,234,795 | $ | 41,943 | |||||||
Total current assets | 1,095,614 | 36,631 | 1,405,944 | 47,756 | |||||||||||
Total assets | 1,385,978 | 46,339 | 1,727,859 | 58,691 | |||||||||||
Total current liabilities | 556,697 | 18,612 | 241,242 | 8,194 | |||||||||||
Long-term borrowings | 55,508 | 1,856 | 451,370 | 15,332 | |||||||||||
Total liabilities | 664,068 | 22,202 | 775,865 | 26,354 | |||||||||||
Total equity | 721,910 | 24,137 | 951,994 | 32,337 |
Selected Consolidated Statements of Operations Data
Three-month periods ended |
Six-month periods ended |
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2019 | 2020 | 2019 | 2020 | |||||||||||||||||||||||||||||||||||||
Operating revenue | $ | 20,592 | $ | 664 | $ | 11,776 | $ | 400 | $ | 178,357 | $ | 5,751 | $ | 23,750 | $ | 807 | ||||||||||||||||||||||||
Operating expenses | ||||||||||||||||||||||||||||||||||||||||
General and administrative expenses | ( | 38,126 | ) | ( | 1,230 | ) | ( | 39,487 | ) | ( | 1,341 | ) | ( | 78,903 | ) | ( | 2,544 | ) | ( | 72,367 | ) | ( | 2,458 | ) | ||||||||||||||||
Research and development expenses | ( | 224,217 | ) | ( | 7,230 | ) | ( | 228,881 | ) | ( | 7,774 | ) | ( | 453,372 | ) | ( | 14,620 | ) | ( | 420,659 | ) | ( | 14,289 | ) | ||||||||||||||||
Total operating expenses | ( | 262,343 | ) | ( | 8,460 | ) | ( | 268,368 | ) | ( | 9,115 | ) | ( | 532,275 | ) | ( | 17,164 | ) | ( | 493,026 | ) | ( | 16,747 | ) | ||||||||||||||||
Loss before income tax | ( | 240,622 | ) | ( | 7,759 | ) | ( | 242,089 | ) | ( | 8,223 | ) | ( | 352,030 | ) | ( | 11,352 | ) | ( | 456,253 | ) | ( | 15,498 | ) | ||||||||||||||||
Income tax expense | ( | 854 | ) | ( | 28 | ) | ( | 348 | ) | ( | 12 | ) | ( | 1,131 | ) | ( | 36 | ) | ( | 769 | ) | ( | 26 | ) | ||||||||||||||||
Net loss | $ | ( | 241,476 | ) | $ | ( | 7,787 | ) | $ | ( | 242,437 | ) | $ | ( | 8,235 | ) | $ | ( | 353,161 | ) | $ | ( | 11,388 | ) | $ | ( | 457,022 | ) | $ | ( | 15,524 | ) | ||||||||
Total other comprehensive income (loss) | $ | 374 | $ | 12 | $ | 1,698 | $ | 58 | $ | 916 | $ | 29 | $ | ( | 1,808 | ) | $ | ( | 61 | ) | ||||||||||||||||||||
Total comprehensive loss | $ | ( | 241,102 | ) | $ | ( | 7,775 | ) | $ | ( | 240,739 | ) | $ | ( | 8,177 | ) | $ | ( | 352,245 | ) | $ | ( | 11,359 | ) | $ | ( | 458,830 | ) | $ | ( | 15,585 | ) | ||||||||
Loss per share of common stock | ||||||||||||||||||||||||||||||||||||||||
Basic and diluted loss per share (in dollars) | $ | ( | 3.79 | ) | $ | ( | 0.12 | ) | $ | ( | 3.28 | ) | $ | ( | 0.11 | ) | $ | ( | 5.55 | ) | $ | ( | 0.18 | ) | $ | ( | 6.18 | ) | $ | ( | 0.21 | ) |
About
Cautionary Note on Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements contained in this press release include, without limitation, statements regarding TLC’s expectations regarding the clinical development of TLC’s product candidates, including TLC599 and TLC590, the clinical benefits of TLC’s product candidates, the timing, scope, progress and outcome of TLC’s clinical trials, how sufficient cash and equivalents will be to fund operations, the anticipated timelines for the release of clinical data and progress of TLC’s manufacturing capabilities. Words such as "may," "believe," "will," "expect," "plan," "anticipate," "estimate," "intend" and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are not guarantees of future performance and involve a number of risks, assumptions, uncertainties and factors, including risks that the outcome of any clinical trial is inherently uncertain and product candidates may prove to be unsafe or ineffective, or may not achieve commercial approval, and delays or disruptions on our business or clinical trials due to the COVID-19 pandemic. Other risks are described in the Risk Factors section of
TLC Contact:Dawn Chi Corporate Communications dawn@tlcbio.com
Source: TLC