Aptose Biosciences(APTO)
Search documents
Aptose Announces Results from Annual and Special Meeting of Shareholders
GlobeNewswire News Room· 2024-06-18 21:30
SAN DIEGO and TORONTO, June 18, 2024 (GLOBE NEWSWIRE) -- Aptose Biosciences Inc. (“Aptose” or the “Company”) (NASDAQ: APTO, TSX: APS), a clinical-stage precision oncology company developing highly differentiated oral kinase inhibitors to treat hematologic malignancies, today announced the voting results from the Company’s annual and special meeting of shareholders held today, June 18, 2024 (the “Meeting”). A total of 8,101,527 common shares of the Company, representing 49.67% of the common shares of the Com ...
Aptose Presents Tuspetinib (TUS) Clinical and Preclinical Findings at European Hematology Association (EHA) 2024 Hybrid Congress
Newsfilter· 2024-06-14 11:30
TUS Monotherapy and TUS+Venetoclax (VEN) Doublet Therapy Show Broad Clinical Activity and Strong Safety Data in relapsed or refractory (R/R) Acute Myeloid Leukemia (AML) and Differentiate TUS from other Investigational Drugs in AML TUS Monotherapy and TUS+VEN Doublet Therapy Active in Difficult-to-treat Genetic Subgroups, FLT3 Wildtype AML TUS Shown to Target VEN Resistance Mechanisms and Retain Activity on VEN-Resistant AML Cells in Preclinical Study TUS+VEN+Azacitidine (AZA) Triplet Trial to Treat Newly D ...
Aptose Presents Tuspetinib (TUS) Clinical and Preclinical Findings at European Hematology Association (EHA) 2024 Hybrid Congress
GlobeNewswire News Room· 2024-06-14 11:30
TUS Monotherapy and TUS+Venetoclax (VEN) Doublet Therapy Show Broad Clinical Activity and Strong Safety Data in relapsed or refractory (R/R) Acute Myeloid Leukemia (AML) and Differentiate TUS from other Investigational Drugs in AML TUS Monotherapy and TUS+VEN Doublet Therapy Active in Difficult-to-treat Genetic Subgroups, FLT3 Wildtype AML TUS Shown to Target VEN Resistance Mechanisms and Retain Activity on VEN-Resistant AML Cells in Preclinical Study TUS+VEN+Azacitidine (AZA) Triplet Trial to Treat Newly D ...
Aptose Biosciences (APTO) Upgraded to Buy: What Does It Mean for the Stock?
ZACKS· 2024-06-13 17:21
Investors might want to bet on Aptose Biosciences (APTO) , as it has been recently upgraded to a Zacks Rank #2 (Buy). This rating change essentially reflects an upward trend in earnings estimates -- one of the most powerful forces impacting stock prices.The sole determinant of the Zacks rating is a company's changing earnings picture. The Zacks Consensus Estimate -- the consensus of EPS estimates from the sell-side analysts covering the stock -- for the current and following years is tracked by the system.T ...
Aptose Announces Closing of $4.43 Million Registered Direct Offering Priced At-the-Market Under Nasdaq Rules
Newsfilter· 2024-06-03 20:30
Core Viewpoint - Aptose Biosciences Inc. has successfully closed a registered direct offering of 3,855,000 common shares at a price of $1.15 per share, raising approximately $4.43 million in gross proceeds, which will be used for working capital and general corporate purposes [1][2]. Group 1: Offering Details - The offering included both registered common shares and unregistered series A and B warrants, each exercisable at $1.15 per share [1]. - The series A warrants will expire five years from shareholder approval, while the series B warrants will expire eighteen months from the same approval [1]. - H.C. Wainwright & Co. acted as the exclusive placement agent for the offering [2]. Group 2: Company Overview - Aptose Biosciences is a clinical-stage biotechnology company focused on developing precision medicines for oncology, particularly in hematology [5]. - The company's pipeline includes two clinical-stage oral kinase inhibitors: tuspetinib, which is being developed for acute myeloid leukemia (AML), and luxeptinib, aimed at treating relapsed or refractory hematologic malignancies [5].
Aptose Announces $4.43 Million Registered Direct Offering Priced At-the-Market Under Nasdaq Rules
Newsfilter· 2024-05-31 12:00
SAN DIEGO and TORONTO, May 31, 2024 (GLOBE NEWSWIRE) -- Aptose Biosciences Inc. ("Aptose" or the "Company") (NASDAQ:APTO, TSX:APS), a clinical-stage precision oncology company developing highly differentiated oral targeted agents to treat hematologic malignancies, today announced that it has entered into a definitive agreement for the issuance and sale of 3,855,000 of its common shares (or common share equivalents in lieu thereof) at a purchase price of $1.15 per share (or per common share equivalent in lie ...
Aptose Biosciences(APTO) - 2024 Q1 - Earnings Call Transcript
2024-05-15 03:12
Aptose Biosciences Inc. (NASDAQ:APTO) Q1 2024 Earnings Conference Call May 14, 2024 5:00 PM ET Company Participants Susan Pietropaolo - MD, Corporate Communications and IR William Rice - Chairman, President and CEO Rafael Bejar - SVP and CMO Fletcher Payne - SVP, CFO, and CBO Conference Call Participants Joe Pantginis - H.C. Wainwright Operator Good afternoon. My name is Josh and I will be your conference operator today. I would like to welcome everyone to the Aptose Biosciences' Conference Call for the Fir ...
Aptose Biosciences(APTO) - 2024 Q1 - Quarterly Report
2024-05-14 21:06
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 10-Q ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the Quarterly Period Ended March 31, 2024 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the Transition Period from to Commission File Number: 1-32001 APTOSE BIOSCIENCES INC. (Exact Name of Registrant as Specified in Its Charter) Canada (State or other jurisdiction of incorporation or ...
Aptose Biosciences(APTO) - 2024 Q1 - Quarterly Results
2024-05-14 20:15
[Corporate and Clinical Update](index=1&type=section&id=Corporate%20and%20Clinical%20Update) Aptose is advancing its lead drug, Tuspetinib, into a frontline triplet therapy for newly diagnosed AML, with key milestones planned through 2025, while also addressing Nasdaq listing compliance [Key Corporate Highlights](index=1&type=section&id=Key%20Corporate%20Highlights) Aptose has advanced its lead drug, Tuspetinib, into a frontline triplet therapy (TUS+VEN+HMA) for newly diagnosed Acute Myeloid Leukemia (AML), with the protocol submitted to the FDA and clinical sites being activated, supported by extensive data showing a favorable safety profile and broad activity, while also addressing Nasdaq listing compliance issues - The TUS+VEN+HMA triplet therapy protocol for newly diagnosed (ND) AML was submitted to the FDA in Q1 2024 and is now being activated at clinical sites[1](index=1&type=chunk)[4](index=4&type=chunk) - The triplet therapy aims to improve upon the current VEN+HMA standard of care by increasing response rates and prolonging survival, particularly for patients who respond poorly to VEN-containing regimens[2](index=2&type=chunk) - Tuspetinib has demonstrated a favorable safety profile with no treatment-related QTc prolongation, differentiation syndrome, or drug-related deaths in prior trials[3](index=3&type=chunk) - Aptose regained compliance with a Nasdaq listing rule concerning a private placement after amending warrant terms with Hanmi Pharmaceutical[7](index=7&type=chunk) - The company received a second Nasdaq non-compliance notice for its stockholders' equity falling below the **$2.5 million** minimum as of December 31, 2023, but equity has since turned positive to **$137,000** as of March 31, 2024[8](index=8&type=chunk) [Upcoming Milestones](index=2&type=section&id=Multiple%20Planned%20Value-creating%20Milestones%20Ahead) Aptose has outlined a series of key milestones for its Tuspetinib triplet therapy program, starting with data presentation at EHA 2024, followed by the initiation and dose escalation of the pilot study in 2024, and culminating in the planned initiation of a pivotal Phase 2/3 program in the second half of 2025 Planned Milestones for Tuspetinib Triplet Program | Milestone | Expected Timing | | :--- | :--- | | TUS+VEN data presentation in R/R AML | EHA 2024 | | Triplet pilot dose initiation in ND AML | Summer 2024 | | Triplet pilot early data (CR/MRD/safety) | ASH 2024 | | Triplet pilot completion and dose selection | EHA 2025 | | Triplet Ph2/Ph3 pivotal program initiation | 2H 2025 | [Financial Results for Q1 2024](index=2&type=section&id=FINANCIAL%20RESULTS%20OF%20OPERATIONS) Aptose reported a reduced net loss in Q1 2024 due to decreased operating expenses, with its financial position showing positive stockholders' equity and sufficient cash to fund operations through August 2024 [Summary of Operations](index=2&type=section&id=Summary%20of%20Operations) For the first quarter of 2024, Aptose reported a net loss of $9.6 million, or $0.73 per share, representing a significant reduction from the $13.7 million net loss, or $2.22 per share, in the same period of 2023, driven by decreased operating expenses Q1 2024 Statement of Operations Highlights (in thousands, except per share data) | Metric | Q1 2024 | Q1 2023 | | :--- | :--- | :--- | | Research and development | $6,445 | $8,811 | | General and administrative | $3,315 | $5,285 | | **Operating expenses** | **$9,760** | **$14,096** | | **Net loss** | **$(9,640)** | **$(13,676)** | | Net Loss per share | $(0.73) | $(2.22) | - The decrease in net loss was primarily due to a **$2.4 million** reduction in R&D costs and a **$2.0 million** reduction in general and administrative costs compared to Q1 2023[13](index=13&type=chunk) [Financial Position](index=3&type=section&id=Financial%20Position) As of March 31, 2024, Aptose had $9.3 million in cash, cash equivalents, and short-term investments, with stockholders' equity turning positive to $0.14 million from a deficit of $2.9 million at the end of 2023, and management expects the current cash position to fund operations through August 2024 Balance Sheet Data (in thousands) | Metric | March 31, 2024 | Dec 31, 2023 | | :--- | :--- | :--- | | Cash, cash equivalents and short-term investments | $9,328 | $9,252 | | Working capital | $(318) | $(3,375) | | Total assets | $12,796 | $12,989 | | Stockholders' equity | $137 | $(2,901) | - The company projects its current cash and available capital are sufficient to fund planned operations through August 2024[14](index=14&type=chunk) [Research and Development (R&D) Expenses Analysis](index=3&type=section&id=RESEARCH%20AND%20DEVELOPMENT%20EXPENSES) R&D expenses for Q1 2024 decreased by $2.4 million to $6.4 million compared to the same period in 2023, primarily driven by lower program costs for Tuspetinib due to the near completion of APTIVATE trials and a significant decrease in costs for the Luxeptinib program as certain clinical activities concluded R&D Expenses Breakdown (in thousands) | Program | Q1 2024 | Q1 2023 | | :--- | :--- | :--- | | Tuspetinib | $3,923 | $4,774 | | Luxeptinib | $208 | $1,289 | | Personnel related expenses | $1,954 | $2,078 | | Stock-based compensation | $328 | $652 | | **Total R&D Expenses** | **$6,445** | **$8,811** | - Tuspetinib program costs decreased due to the near completion of APTIVATE clinical trials and reduced manufacturing costs[17](index=17&type=chunk) - Luxeptinib program costs fell by approximately **$1.1 million** due to the conclusion of certain clinical trial and manufacturing activities[18](index=18&type=chunk) [Corporate Information](index=4&type=section&id=Corporate%20Information) Aptose Biosciences is a clinical-stage biotechnology company focused on precision oncology, with its report containing forward-looking statements subject to inherent risks and uncertainties [About Aptose](index=4&type=section&id=About%20Aptose) Aptose Biosciences is a clinical-stage biotechnology company focused on developing precision oncology medicines, particularly for hematologic malignancies, with a pipeline featuring two oral kinase inhibitors: tuspetinib for AML and luxeptinib for other relapsed or refractory hematologic malignancies - Aptose is a clinical-stage biotech company developing precision medicines for unmet needs in oncology, with an initial focus on hematology[21](index=21&type=chunk) - The company's pipeline includes two oral kinase inhibitors: tuspetinib for AML and luxeptinib for relapsed or refractory hematologic malignancies[21](index=21&type=chunk) [Forward-Looking Statements](index=5&type=section&id=Forward%20Looking%20Statements) This press release includes forward-looking statements concerning the company's clinical development plans, the potential of its drug candidates, trial timelines, and its financial runway, which are subject to significant risks and uncertainties, and actual results may differ materially from expectations - The report contains forward-looking statements regarding clinical development plans, the potential of tuspetinib, clinical trial timelines, and the company's capital resources[22](index=22&type=chunk) - These statements are subject to risks and uncertainties, and the company does not assume any obligation to update them[23](index=23&type=chunk)
Aptose Reports Results for the First Quarter 2024
Newsfilter· 2024-05-14 20:01
TUS+VEN+HMA Triplet Protocol in 1L Therapy for Newly Diagnosed AML was Submitted to the FDA During Q1 and is Now Being Activated at Clinical Sites TUS+VEN+HMA Triplet 1L Therapy for Newly Diagnosed AML is Supported by Extensive TUS and TUS+VEN Data from Completed Trials with R/R AML Conference Call and Webcast at 5:00 pm ET Today SAN DIEGO and TORONTO, May 14, 2024 (GLOBE NEWSWIRE) -- Aptose Biosciences Inc. ("Aptose" or the "Company") (NASDAQ:APTO, TSX:APS), a clinical-stage precision oncology company de ...