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APTOF

Aptose Biosciences Inc.

Biopharma developer (SEC filing verified)·Toronto, ON, Canada·CEO: Dr. William G. Rice Ph.D.

APTOF evidence brief

What we can confirm

Market Cap:
$4.3M

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $4.3M
BioSniper AIPage evidence connected

Prepared research question

What matters most for APTOF—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · APTOF

Aptose Biosciences Inc. is a clinical-stage precision oncology company developing tuspetinib, a novel kinase inhibitor, for frontline combination therapy in newly diagnosed acute myeloid leukemia (AML), but faces imminent financial distress.

Key risk: Imminent bankruptcy risk

Market Cap

$4.3M

Cash Runway

—

Lead Asset

—

Next Catalyst

—

Financial data as of Mar 31, 2026.

Tracking 1 clinical trial for Aptose Biosciences Inc..

AI OverviewAI overview is shown in English only.

Aptose Biosciences Inc. is a clinical-stage precision oncology company developing tuspetinib, a novel kinase inhibitor, for frontline combination therapy in newly diagnosed acute myeloid leukemia (AML), but faces imminent financial distress.

  • Aptose's lead program is tuspetinib (TUS), being developed for frontline combination therapy in newly diagnosed AML patients [sec_mda · as of 2026-03-31].
  • The FDA granted orphan drug designation to tuspetinib for the treatment of AML in October 2018 [sec_mda · as of 2026-03-31].
  • As of 2026-03-31, the company reported total revenue of $0.0M, net income of -$7.6M, and shareholders' equity of -$34.7M [sec].
  • The company has disclosed a risk of imminent bankruptcy and needs substantial funding immediately to continue operations [sec_mda · as of 2026-05-13].
  • Aptose is continuing a Phase 1/2 clinical trial (TUSCANY) evaluating tuspetinib in combination with venetoclax and azacitidine in newly diagnosed AML patients [sec_mda · as of 2026-03-31].

What works

  • Tuspetinib has demonstrated an excellent safety profile and retains nanomolar potency against AML cells with resistance mechanisms to venetoclax, positioning it as a potential component of triplet therapy [sec_mda · as of 2026-03-31].
  • The company completed a successful End of Phase 1 Meeting with the US FDA for tuspetinib, with all development paths remaining open, including a single-arm accelerated approval path [sec_mda · as of 2026-03-31].
  • The National Cancer Institute (NCI) has selected the TUSCANY study for presentation at the 2025 ASH Annual Meeting, indicating external scientific interest [news · published 2025-11-03].

What to weigh

  • Aptose has disclosed a risk of imminent bankruptcy and states it needs substantial funding immediately to continue operations [sec_mda · as of 2026-05-13].
  • The company has no revenue and a negative shareholders' equity of -$34.7M as of 2026-03-31, reflecting a structurally challenged financial position [sec].
  • Aptose has maximum obligations for clinical development and global regulatory milestones totaling $64.5 million for the first potential indication of tuspetinib, with additional sales-based milestones and royalty payments [sec_mda · as of 2026-03-31].
  • The company's suppliers may choose to stop working on programs or change contract terms, and there are risks to maintaining an adequate supply of clinical drug product [sec_mda · as of 2026-05-13].

From the filings

Quoted directly from source documents.

  • Risk of imminent bankruptcy

    “our risk of imminent bankruptcy;”

    SEC MD&A · May 13, 2026

  • Tuspetinib orphan drug designation

    “The FDA granted orphan drug designation to tuspetinib for the treatment of patients with AML in October 2018.”

    SEC MD&A · March 31, 2026

  • Successful End of Phase 1 Meeting with FDA

    “Aptose also reported completion of a successful End of Phase 1 Meeting with the US FDA for tuspetinib, that a monotherapy RP2D was selected as 80mg daily, and that all development paths remain open, including the single arm accelerated path.”

    SEC MD&A · March 31, 2026

  • Need for immediate funding

    “we need to obtain substantial funding immediately in order to continue operations and our exploration of strategic alternatives;”

    SEC MD&A · May 13, 2026

Risks & what to watch (4)›

Key risks

  • Imminent bankruptcy risk — Company has disclosed a risk of imminent bankruptcy and needs substantial funding immediately to continue operations [sec_mda · as of 2026-05-13].
  • Negative shareholders' equity — Shareholders' equity is -$34.7M as of 2026-03-31, indicating liabilities exceed assets [sec].
  • Supply chain vulnerability — Suppliers may stop working or change terms, and there are risks to maintaining clinical drug product supply [sec_mda · as of 2026-05-13].
  • Milestone payment obligations — Up to $64.5M in development milestones due for first indication, plus sales milestones and royalties [sec_mda · as of 2026-03-31].

What to watch

  • Ability to secure additional financing to avoid bankruptcy and continue operations [sec_mda · as of 2026-05-13].
  • Clinical data from the TUSCANY trial, including CR/CRh and MRD negativity rates, expected over the next 6 to 12 months [sec_mda · as of 2026-03-31].
  • Presentation of TUSCANY study data at the 2025 ASH Annual Meeting [news · published 2025-11-03].
  • Progress of the arrangement to continue from the Canada Business Corporations Act to the Business Corporations Act (Alberta), expected to close in first half of 2026 [sec_mda · as of 2026-03-31].

Sources: News · SEC MD&A · Generated October 2, 2026 · How we verify sources →

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Evidence & data

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

4

Total value held

$40K

Short Interest

as of May 20, 2026
% of float
2.6%
Days to cover
0.1
Shares short
53,154
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

APTOF short interest

Governance

Frequently asked questions

What is the AI investment thesis for Aptose Biosciences Inc.?

Aptose Biosciences Inc. is a clinical-stage precision oncology company developing tuspetinib, a novel kinase inhibitor, for frontline combination therapy in newly diagnosed acute myeloid leukemia (AML), but faces imminent financial distress.

Who is the CEO of Aptose Biosciences Inc.?

Dr. William G. Rice Ph.D. is the chief executive officer of Aptose Biosciences Inc. (APTOF).

Where is Aptose Biosciences Inc. headquartered?

Aptose Biosciences Inc. (APTOF) is headquartered in Toronto, ON, Canada.

923 companies304,840 SEC filings22,639 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.