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8-K ·Filed Jun 15, 2026

APTOF

Aptose Biosciences Inc.
BULLISH
Impact 7/10
Horizonweeks Processed4mo ago SEC0001171843-26-004119
8-K context-dependent: Items 7.01
Actionable Insight ▲ Bullish

The strong efficacy and safety data across difficult-to-treat AML populations (TP53-mut, complex karyotype) significantly de-risks the TUS+VEN+AZA triplet program. Monitor for next clinical milestones, potential partnership interest, and upcoming financing needs as the company advances toward pivotal trials.

DirectionBullish
Confidencehigh
Horizonweeks
Latest settled — T+5d
APTOF ▼ -8.07% at T+5d
LONG call ✗ call lost -8.07% · α vs SPY -5.46% · entry $1.61 → $1.48
Next anchor: T+20d due 3mo ago
Entry = T+0 close
Jun 15, 2026
via day close
T+1d
-2.48%
call -2.48% · α -1.89%
$1.57
settled 4mo ago
T+5d
-8.07%
call -8.07% · α -5.46%
$1.48
settled 4mo ago
T+20d
Pending
due 3mo ago
T+60d
Pending
due 7w ago

Price Chart

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Executive Summary

Aptose Biosciences presented updated Phase 1/2 TUSCANY trial data for tuspetinib (TUS) triplet therapy in newly diagnosed AML at the EHA 2026 Congress. The data showed an 86.2% composite complete response (CRc) rate in evaluable patients and an 86.4% MRD-negativity rate among responders, including 100% CR in TP53-mutated patients at the 160 mg dose. No financial data or guidance was provided in this clinical data update.

Key Facts

  • Composite complete response (CRc) rate across all evaluable patients was 86.2% (25 of 29 patients).
  • MRD-negativity rate among patients achieving CR/CRh was 86.4%.
  • At the 160 mg dose (n=13), CRc rate was 76.9% (10 of 13 patients).
  • 100% composite complete remission in all 4 patients with TP53-mutation with complex karyotype at the 160 mg dose.
  • No treatment-related deaths or QTc prolongation, CPK elevations, or differentiation syndrome reported.
  • Data presented in an oral presentation at the EHA 2026 Congress in Stockholm, Sweden.

Financial Impact

No financial figures reported; clinical-stage company with no revenue or earnings data in this filing.

Risk Factors

  • Clinical-stage company with no approved products or revenue; requires additional capital to fund ongoing trials.
  • Forward-looking statements caution about ability to obtain capital and continue as a going concern.
  • Early-stage data (Phase 1/2, n=32) may not replicate in larger pivotal trials.

Market Snapshot

Exchange
OTC
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
86% bullish (7 analysts)

Investment Themes

Documents Analyzed

This report is based on 5 SEC documents filed with EDGAR.

DocumentAccession Number
8-K Filing (Primary)0001171843-26-004119
Exhibit: exh_991.htm0001171843-26-004119
Document: 0001171843-26-004119-index-headers.html0001171843-26-004119
Document: 0001171843-26-004119-index.html0001171843-26-004119
Document: 0001171843-26-004119.txt0001171843-26-004119
5 reports for APTOF
Performance horizon

Track record builds as more directional reports settle.

Filters
Rows
Reports for APTOF — sortable, filterable
TypeNow
Jul 1, 2026
16w ago
15-12G
BEARISH ★ 7/10
$1.68 $1.69▼ −0.60%▼ −0.64%—
Jun 15, 2026
19w ago
8-K
BULLISH ★ 7/10
$1.61 $1.48▼ −8.07%▼ −5.46%—
May 29, 2026
21w ago
8-K
NEUTRAL ★ 5/10
$1.65 $1.57▼ −4.85%▼ −2.32%—
May 13, 2026
23w ago
8-K
NEUTRAL ★ 5/10
$1.71 $1.71· 0.00%▲ +0.72%—
Mar 19, 2026
31w ago
8-K
BULLISH ★ 8/10
$1.62 $1.64▲ +1.23%▲ +3.45%—
Showing 5 of 5

US Market Status

Market Closed — Opens Wed (< 1m)

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Report published Jun 15, 2026