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8-K ·Filed Sep 18, 2026

ATOS

ATOSSA THERAPEUTICS, INC.
NEUTRAL
Impact 3/10
Horizonweeks Processed1mo ago SEC0001193125-26-395694
8-K context-dependent: Items 7.01
Actionable Insight • Neutral

Monitor EVANGELINE Phase 2 top-line data expected in 4Q26 and IND clearance for MAS/DMD programs in 2H26 as key near-term catalysts. Cash runway into 2027 provides no immediate financing urgency.

DirectionNeutral
Confidencehigh
Horizonweeks
Latest settled — T+20d
ATOS ▲ +13.78% at T+20d
NEUTRAL call +13.78% · α vs SPY +14.69% · entry $2.25 → $2.56
Next anchor: T+60d in 7w
Latest observation: T+24 +7.86% FF3 residual α
Entry = T+0 close
Sep 18, 2026
via day close
T+1d
+0.44%
call +0.44% · α +0.46%
$2.26
settled 5w ago
T+5d
-12.89%
call -12.89% · α -11.87%
$1.96
settled 5w ago
T+20d
+13.78%
call +13.78% · α +14.69%
$2.56
settled 11d ago
T+60d
Pending
in 7w

Price Chart

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Executive Summary

Atossa Therapeutics filed an 8-K on September 18, 2026, to make available an updated corporate investor presentation (Exhibit 99.1). The presentation highlights the company's lead drug candidate (Z)-Endoxifen across oncology (breast cancer) and rare disease (MAS, DMD) programs, reports $26.1M cash and equivalents with no debt at June 30, 2026, and notes EVANGELINE Phase 2 enrollment completed with top-line data anticipated in 4Q26. This is a routine disclosure of existing strategy and financial position with no new material financial data or catalysts.

Key Facts

  • $26.1M cash and equivalents at June 30, 2026
  • No debt outstanding at June 30, 2026
  • Total operating expenses of $8.7M in Q2 2026
  • June 2026 registered direct offering raised $4.0M (net)
  • Up to $12M additional from Series A and short-term Series B warrants, assuming full cash exercise
  • EVANGELINE Phase 2 enrollment completed as of June 30, 2026; top-line data anticipated in 4Q26
  • IND clearance in MAS and DMD anticipated in 2H26
  • FDA Rare Pediatric Disease designation for both MAS and DMD; Orphan Drug Designation for DMD
  • ~800 patients dosed with (Z)-endoxifen to date

Financial Impact

No new financial data or guidance provided; cash position of $26.1M as of June 30, 2026, with $8.7M quarterly operating burn rate

cashdebtoperating expenses

Risk Factors

  • Pre-revenue clinical-stage biotech with no approved products
  • Relies on capital markets for future funding beyond 2027
  • Clinical trial results may not support regulatory approval
  • Warrant exercise is optional and may not provide additional capital

Investment Themes

Documents Analyzed

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

DocumentAccession Number
8-K Filing (Primary)0001193125-26-395694
Document: atos-ex99_1.htm0001193125-26-395694
Document: 0001193125-26-395694-index-headers.html0001193125-26-395694
Document: 0001193125-26-395694-index.html0001193125-26-395694
Document: 0001193125-26-395694.txt0001193125-26-395694
7 reports for ATOS
Performance horizon

Track record builds as more directional reports settle.

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Reports for ATOS — sortable, filterable
TypeNow
Oct 9, 2026
17d ago
8-K
NEUTRAL ★ 4/10
$2.44awaiting T+60—$2.45 (+0.41%)
Sep 29, 2026
27d ago
8-K
NEUTRAL ★ 4/10
$1.99awaiting T+60—$2.45 (+23.12%)
Sep 18, 2026
5w ago
8-K
NEUTRAL ★ 3/10
$2.25awaiting T+60—$2.45 (+8.89%)
Aug 7, 2026
11w ago
8-K
NEUTRAL ★ 4/10
$2.36awaiting T+60—$2.45 (+3.81%)
Aug 7, 2026
11w ago
Press Release
NEUTRAL ★ 4/10
$2.36awaiting T+60—$2.45 (+3.81%)
Jun 12, 2026
19w ago
424B5
BEARISH ★ 6/10
$2.46 $2.52▼ −2.24%▲ +1.03%$2.45 (+0.41%)
Apr 16, 2026
27w ago
8-K
BULLISH ★ 7/10
$5.77 $2.40▼ −58.41%▼ −65.45%$2.45 (−57.54%)
Showing 7 of 7

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Report published Sep 18, 2026