Dr. William Rice reports

APTOSE REPORTS RESULTS FOR THE FOURTH QUARTER AND FULL YEAR 2022

Aptose Biosciences Inc. today released its financial results for the fourth quarter and year ended Dec. 31, 2022, and has provided a corporate update.

The net loss for the quarter ended Dec. 31, 2022, was $10.0-million (11 cents per share) compared with $24.3-million (27 cents per share) for the quarter ended Dec. 31, 2021. The net loss for the year ended Dec. 31, 2022, was $41.8-million (45 cents per share) compared with $65.4-million (73 cents per share) for the year ended Dec. 31, 2021. Total cash and cash equivalents and investments as of Dec. 31, 2022, were $47.0-million. Based on current operations, Aptose expects that cash on hand and available capital provide the company with sufficient resources to finance planned company operations including research and development into the first quarter of 2024.

"To expand on the clinically significant response data observed across a broad population of acute myeloid leukemia (AML) patients during the dose escalation and exploration phase of our trial, we rapidly transitioned to our Aptivate phase 1/2 expansion trial with tuspetinib. Aptivate already is running smoothly with several AML patients being treated in the monotherapy arm, and patient enrolment now is under way in the doublet combination treatment arm with tuspetinib and venetoclax (TUS/VEN). And we are eager to bring additional data to you throughout the year," said William G. Rice, PhD, chairman, president and chief executive officer. "We anticipate enrolling up to 100 patients in the Aptivate study, from which we expect to demonstrate single agent activity that can guide multiple paths for potential accelerated approval in patients with adverse mutations, and to demonstrate activity in doublet and then triplet combination therapies, which we believe represent the future directions of AML treatment. Tuspetinib's single-agent activity targets more AML populations than SYK inhibitors, IRAK4 inhibitors or menin inhibitors, and, its distinctly favourable safety profile also lends itself to an ideal combination treatment to potentially treat larger AML patient populations in earlier lines of therapy."

Key corporate highlights

• Tuspetinib Aptivate expansion trial initiated -- In January, Aptose announced the initiation of dosing in the monotherapy arm in the Aptivate phase 1/2 clinical trial of tuspetinib (formerly HM43239), a once-daily oral, mutation agnostic tyrosine kinase inhibitor being developed for the treatment of patients with relapsed or refractory acute myeloid leukemia (R/R AML). The Aptivate expansion trial is designed to confirm monotherapy activity through patient enrichment of specific mutationally defined AML populations, including TP53-mutant patients and FLT3-mutant patients who have been failed by a prior FLT3 inhibitor, as supported by FDA fast-track designation and a clinically significant response rate to date. In the Aptivate expansion trial, tuspetinib also will be tested in combination with venetoclax (TUS/VEN), and the TUS/VEN doublet arm already has begun enrolment. While Aptivate is early in the treatment of patients with tuspetinib monotherapy, the company already has observed initial signs of antileukemic activity, and it will provide additional colour as the clinical data evolve.
  • Tuspetinib is designed to simultaneously target SYK, JAK1/2, FLT3, RSK and other kinases operative in AML. As a monotherapy treatment during dose escalation and exploration in the company's phase 1/2 trial, tuspetinib safely delivered multiple complete remissions and clinical responses across four dose levels (40 milligrams, 80 mg, 120 mg and 160 mg) in AML patients that previously had been failed by chemotherapy, BCL2 inhibitors, hypomethylating agents, FLT3 inhibitors and hematopoietic stem cell transplants. Data presented in December at the 2022 American Society of Hematology (ASH) annual meeting by lead investigator Naval G. Daver, MD, associate professor in the Department of Leukemia at MD Anderson Cancer Center, showed tuspetinib delivers single-agent responses without prolonged myelosuppression or life-threatening toxicities in these very ill and heavily pretreated R/R AML patients. Responses were observed in a broad range of mutationally defined populations, including those with mutated forms of NPM1, MLL, TP53, DNMT3A, RUNX1, wild-type FLT3, ITD or TKD mutated FLT3, various splicing factors, and other genes. Unexpectedly, the company observed a 29-per-cent CR/CRh response rate with tuspetinib monotherapy in patients having mutations in the RAS gene or other genes in the RAS pathway. Responses in RAS-mutated patients are important because the RAS pathway is often mutated in response to therapy by other agents as the AML cells mutate toward resistance to those other agents.
  • With dose escalation and exploration successfully completed, the company now is focusing on execution of the Aptivate phase 1/2 expansion trial. While it plans to report data throughout the year, the company also will plan an incremental update from Aptivate around the European Hematology Association (EHA) conference in June, a more complete data set at the European School of Haematology (ESH) meeting in October, and even more data, including from the TUS/VEN combination cohort, during the ASH meeting in December.
• Rationale for Tuspetinib's superior safety -- Clinical responses by kinase inhibitors typically require high plasma exposures and near-complete suppression of a target kinase, but such agents often cause undesired toxicities because they cause extensive inhibition of that same target in normal cells. In contrast, tuspetinib to date has demonstrated no drug-related adverse events or dose-limiting toxicities over four active dose levels, and Aptose recently elucidated a rationale for the superior safety profile of tuspetinib. Rather than causing near-complete suppression of a single kinase, tuspetinib achieves clinical responses at lower plasma exposures by simultaneous fractional suppression of a small suite of kinases critical for leukemogenesis. This approach triggers apoptotic death of AML cells but does not result in extensive pathway suppression in normal cells that would lead to greater toxicities. Consequently, fractional suppression of a handful of key kinases and avoidance of safety-related kinases by tuspetinib circumvents many of the toxicities observed with competing agents.
• Continuous dosing of Luxeptinib "G3" formulation continuing; additional Luxeptinib activity noted -- In the fourth quarter of 2022, Aptose announced the initiation of dosing of the G3 formulation of luxeptinib, an oral, lymphoid and myeloid kinase inhibitor, in the continuing phase 1 a/b clinical trial in patients with R/R AML. G3 was developed for more rapid and efficient absorption of luxeptinib and it demonstrated a significant improvement in bioavailability, thereby enabling lower doses, longer retention and higher steady state levels of the drug. Initial pharmacokinetic (PK) data from continuous dosing of the 50 mg G3 formulation show plasma exposure levels roughly equivalent to the 900 mg dose (18-fold greater dose) of the original G1 formulation. Aptose will be reviewing all data with the data monitoring committee and will make the determination to escalate and at what dose.
  • Separately, a small number of B-cell patients are still receiving the original G1 formulation of luxeptinib at the 900 mg dose level. During ASH in December, the company announced that a CR was achieved with a diffuse large B-cell lymphoma patient at the 900 mg dose level of the original G1 formulation, and the company had previously reported an MRD-negative CR with an R/R AML patient receiving 450 mg BID of the original G1 formulation. Together, these findings demonstrate activity of luxeptinib in lymphoid malignancies and AML.
  • Research on luxeptinib continues, and a non-clinical paper was published earlier this month in PLOS One, a highly respected on-line scientific publication. Titled, "Luxeptinib interferes with LYN-mediated activation of SYK and modulates BCR signaling in lymphoma," the paper helps to elucidate the mechanism by which Lux suppresses the B-cell receptor pathway in a manner distinct from the BTK inhibitor ibrutinib. Lux was more effective than ibrutinib at reducing both steady state and anti-IgM-induced phosphorylation of the LYN and SYK kinases upstream of BTK where ibrutinib has little or no effect, suggesting Lux can play a role in B-cell malignancies and inflammatory diseases distinct from ibrutinib and other BTK inhibitors.
• Aptose appoints vice-president, controller -- During the fourth quarter, Aptose appointed Brooks Ensign, vice-president and controller. Mr. Ensign has more than 20 years of pharmaceutical industry experience in accounting, finance and corporate development, and has served in finance roles for multiple public and private companies, including Sunesis Pharmaceuticals, ISTA Pharmaceuticals and Amylin Pharmaceuticals. Mr. Ensign holds an MBA from Harvard Business School and a masters in accounting from National University.

Results of operations

A summary of the results of operations for the years ended Dec. 31, 2022, and 2021 is presented in the attached table.

Net loss of $41.8-million for the year ended Dec. 31, 2022, decreased by approximately $23.5-million as compared with $65.4-million for the year ended Dec. 31, 2021, primarily as of a result of a reduction in research and development program costs and personnel expenses of $5.4-million, the $12.5-million in licence fees paid to Hanmi in 2021 for development rights of tuspetinib, and a $5.0-million decrease in general and administrative costs.

Research and development expenses

Research and development expenses consist primarily of costs incurred related to the research and development of the company's product candidates. Costs are shown in the attached table.

• External research and development expenses incurred under agreements with third parties, such as CROs, consultants, members of the company's scientific advisory boards, external labs and CMOs;
• Employee-related expenses, including salaries, benefits, travel and stock-based compensation for personnel directly supporting the company's clinical trials and manufacturing, and development activities;
• Licence fees.

The company has continuing clinical trials for its product candidates tuspetinib and luxeptinib. Tuspetinib was licensed into Aptose in November, 2021, and the company assumed sponsorship, and the related costs, of the tuspetinib study effective Jan. 1, 2022. In December, 2021, the company discontinued the APTO-253 program and is exploring strategic alternatives for this compound.

The company expects its research and development expenses to be higher as compared with 2022 for the foreseeable future as it continues to advance tuspetinib into larger clinical trials.

The research and development (R&D) expenses for the years ended Dec. 31, 2022, and 2021 were as displayed herein.

R&D expenses decreased by $17.9-million to $28.1-million for the year ended Dec. 31, 2022, as compared with $46.0-million for the comparative period in 2021. Changes to the components of the company's R&D expenses presented in the attached table are primarily as a result of the following activities:

• Licence fees paid in the year ended Dec. 31, 2021, to Hanmi of $12.5-million for global development rights of tuspetinib, including $5.0-million in cash and $7.5-million in common shares. There were no licence fee paid in the year ended Dec. 31, 2022.
• Program costs for tuspetinib increased by $10.0-million. The company in-licensed the development rights for tuspetinib in the fourth quarter of 2021 and assumed sponsorship, and the related costs, of the study effective Jan. 1, 2022.
• Program costs for luxeptinib decreased by approximately $10.1-million, primarily due to lower manufacturing costs because the current formulation requires less API than the prior formulation, and lower clinical trial costs.
• Program costs for APTO-253 decreased by approximately $3.4-million due to the company's decision on Dec. 20, 2021, to discontinue further development of APTO-253.
• Personnel-related expenses decreased by $400,000, due to lower headcount in 2022.
• Stock-based compensation decreased by approximately $1.6-million in the year ended Dec. 31, 2022, compared with the year ended Dec. 31, 2021, primarily due to stock options granted with lower grant date fair values in the current period.

General and administrative expenses

General and administrative expenses consist primarily of salaries, benefits and travel, including stock-based compensation for the company's executive, finance, business development, human resource and support functions. Other general and administrative expenses and professional fees for auditing, and legal services, investor relations and other consultants, insurance, and facility-related expenses.

The company expects that its general and administrative expenses will increase for the foreseeable future as it incurs additional costs associated with being a publicly traded company and to support the company's expanding pipeline of activities. The company also expects its intellectual property related legal expenses to increase as its intellectual property portfolio expands.

The general and administrative expenses for the years ended Dec. 31, 2022, and 2021 are as shown in the attached table.

• General and administrative expenses for the year ended Dec. 31, 2022, were approximately $14.5-million as compared with $19.5-million for the comparative period in 2021, a decrease of approximately $5.0-million. The decrease was primarily as a result of a decrease in stock-based compensation costs of $6.2-million, but was partially offset by higher salaries expenses, higher travel expenses and higher professional fees.
• Stock-based compensation decreased by approximately $6.2-million mostly as a result of a lower number of options granted in the year ended Dec. 31, 2022, with those options having a lower grant date fair value as compared with the options granted in the comparative period, and additional compensation recognized in the comparative period for modifications made to then vested and unvested stock options for one former company officer, as part of a separation and release agreement.

COVID-19 did not have a significant impact on the company's results of operations for the years ended Dec. 31, 2022, and 2021. The company has not experienced and does not foresee material delays to the enrolment of patients or timelines for the tuspetinib phase 1/2 trial or the luxeptinib phase 1a/b trials due to the variety of clinical sites that it has actively recruited for these trials. As of the date of this press release, the company has not experienced material delays in the manufacturing of tuspetinib or luxeptinib related to COVID-19. Should the company's manufacturers be required to shut down their facilities due to COVID-19 for an extended period of time, the company's trials may be negatively impacted.

Conference call and webcast

Date:  Thursday, March 23, 2023

Time:  5 p.m. ET

* Analysts interested in participating in the question-and-answer session will preregister for the event to receive the dial-in numbers and a personal pin, which are required to access the conference call. They also will have the option to take advantage of a call me button and the system will automatically dial out to connect to the Q&A session.

The audio webcast also can be accessed through a link on the investor relations section of Aptose's website. A replay of the webcast will be available on the company's website for 30 days.

The press release, the financial statements and the management's discussion and analysis for the quarter and year ended Dec. 31, 2022, will be available on SEDAR and EDGAR.

About Aptose Biosciences Inc.

Aptose is a clinical-stage biotechnology company committed to developing precision medicines addressing unmet medical needs in oncology, with an initial focus on hematology. The company's small-molecule cancer therapeutic pipeline includes products designed to provide single-agent efficacy and to enhance the efficacy of other anti-cancer therapies and regimens without overlapping toxicities. The company has two clinical-stage oral kinase inhibitors under development for hematologic malignancies: tuspetinib (HM43239), an oral, myeloid kinome inhibitor being studied as monotherapy and in combination therapy in the Aptivate international phase 1/2 expansion trial in patients with relapsed or refractory acute myeloid leukemia (AML); and luxeptinib (CG-806), an oral, dual lymphoid and myeloid kinome inhibitor in a phase 1a/b trial in patients with relapsed or refractory B-cell malignancies who have failed or are intolerant to standard therapies and, in a separate phase 1a/b trial, in patients with relapsed or refractory AML or high-risk myelodysplastic syndrome (MDS).

We seek Safe Harbor.