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8-K ·Filed Aug 11, 2026

AIM

AIM ImmunoTech Inc.
NEUTRAL
Impact 3/10
Horizonweeks Processed2mo ago SEC0001493152-26-036996
8-K context-dependent: Items 7.01
Actionable Insight • Neutral

This is a routine promotional article with no new clinical data or regulatory milestones. Monitor for any actual government funding announcements or FDA interactions, but the filing itself provides no trading catalyst.

DirectionNeutral
Confidencemedium
Horizonweeks
Latest settled — T+20d ⚠ clustered
AIM ▼ -6.72% at T+20d
NEUTRAL call ✗ call lost -6.72% · α vs SPY -5.66% · entry $0.2500 → $0.2332
Next anchor: T+60d in 9d
Latest observation: T+52 -59.61% FF3 residual α
Entry anchored
Aug 11, 08:40 AM ET
via 1-min bar
T+1d
+2.80%
call +2.80% · α +2.55%
$0.2570
settled 3mo ago
T+5d
-6.44%
call -6.44% · α -6.04%
$0.2339
settled 2mo ago
T+20d
-6.72%
call -6.72% · α -5.66%
$0.2332
settled 7w ago
T+60d
Pending
in 9d

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Executive Summary

AIM ImmunoTech filed an 8-K furnishing a sponsored article by CEO Thomas Equels in Breaking Defense, promoting Ampligen (rintatolimod) as a potential broad-spectrum prophylactic antiviral for Ebola and COVID-19. The article cites preclinical mouse-model data showing 100% survival in one treated cohort vs. 100% mortality in controls, but Ampligen is not FDA-approved for any biodefense indication. This is a routine Regulation FD disclosure with no new financial data, clinical results, or material corporate developments.

Key Facts

  • CEO Thomas Equels authored a sponsored article in Breaking Defense on August 11, 2026, discussing Ampligen's potential as a broad-spectrum prophylactic antiviral.
  • Preclinical mouse-model data from USAMRIID showed 100% survival in one rintatolimod-treated cohort vs. 100% mortality in controls for Ebola.
  • Ampligen is not FDA-approved for Ebola virus disease, Bundibugyo virus disease, coronaviruses, or any biodefense indication.
  • The filing contains no financial data, guidance, or material corporate events.

Financial Impact

No financial impact disclosed in the filing.

Risk Factors

  • Ampligen has no FDA approval for any biodefense indication; preclinical results may not replicate in humans.
  • The company has limited financial resources and depends on government funding for further development.
  • Forward-looking statements about broad-spectrum antiviral potential are speculative and not evidence of clinical efficacy.

Market Snapshot

Exchange
NYSE
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
83% bullish (6 analysts)

Investment Themes

Biotech & Drug Discovery

Documents Analyzed

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

DocumentAccession Number
8-K Filing (Primary)0001493152-26-036996
Exhibit: ex99-1.htm0001493152-26-036996
Document: 0001493152-26-036996-index-headers.html0001493152-26-036996
Document: 0001493152-26-036996-index.html0001493152-26-036996
Document: 0001493152-26-036996.txt0001493152-26-036996
31 reports for AIM
Performance horizon
63% Hit rate @ T+20 10 of 16 directional calls Went positive at some point 14 of 19 best @ T+20▲ +57.69%May 14, 2026
Filters
Rows
Reports for AIM — sortable, filterable
TypeNow
Sep 30, 2026
25d ago
DEF 14A
NEUTRAL ★ 3/10
$0.1877awaiting T+20—$0.1600 (−14.76%)
Sep 22, 2026
4w ago
Press Release
NEUTRAL ★ 3/10
$0.2156 $0.1662▼ −22.91%▼ −22.35%$0.1600 (−25.79%)
Sep 14, 2026
5w ago
8-K
BEARISH ★ 7/10
$0.2100awaiting T+20—$0.1600 (+23.81%)
Aug 11, 2026
10w ago
8-K
NEUTRAL ★ 3/10
$0.2500 $0.2332▼ −6.72%▼ −5.66%$0.1600 (−36.00%)
Aug 10, 2026
10w ago
8-K
BEARISH ★ 5/10
$0.2630awaiting T+20—$0.1600 (+39.16%)
Aug 10, 2026
10w ago
Press Release
BEARISH ★ 5/10
$0.2630awaiting T+20—$0.1600 (+39.16%)
Aug 5, 2026
11w ago
8-K
MIXED ★ 6/10
$0.2800 $0.2346▼ −16.21%▼ −15.61%$0.1600 (−42.86%)
Aug 3, 2026
11w ago
Press Release
NEUTRAL ★ 4/10
$0.2600 $0.2260▼ −13.08%▼ −14.31%$0.1600 (−38.46%)
Jun 24, 2026
17w ago
EFFECT
BEARISH ★ 7/10
$0.3740 $0.2534▲ +32.25%▲ +34.18%$0.1600 (+57.22%)
Jun 18, 2026
18w ago
S-1
BEARISH ★ 7/10
$0.3799 $0.2730▲ +28.14%▲ +28.67%$0.1600 (+57.88%)
Showing 10 of 31

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