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PRESS-RELEASE ·Filed Sep 21, 2026

HELP

Helus Pharma
NEUTRAL
Impact 4/10
Horizonmonths Processed1mo ago WireGlobeNewswire
Press release · FDA
Actionable Insight • Neutral

The poster data is incremental and does not change the binary risk/reward of the Phase 3 PARADIGM program. The recent activist 13D filings (Sept 9) add a layer of potential strategic change — watch for any activist-driven announcements or shareholder proposals. The next major catalyst is the Phase 3 readout for HLP003.

DirectionNeutral
Confidencehigh
Horizonmonths
Latest settled — T+20d ⚠ clustered
HELP ▼ -21.74% at T+20d
NEUTRAL call -21.74% · α vs SPY -20.83% · entry $13.66 → $10.69
Next anchor: T+60d in 7w
Latest observation: T+24 -47.90% FF3 residual α
Entry = T+0 close
Sep 21, 2026
via day close
T+1d
+0.37%
call +0.37% · α +0.38%
$13.71
settled 5w ago
T+5d
-7.83%
call -7.83% · α -6.81%
$12.59
settled 29d ago
T+20d
-21.74%
call -21.74% · α -20.83%
$10.69
settled 8d ago
T+60d
Pending
in 7w

Price Chart

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Executive Summary

Helus Pharma presented four posters at Psych Congress 2026, including 12-month efficacy data from its Phase 1/2a study of HLP003 for MDD and a trial-in-progress overview of the ongoing Phase 3 PARADIGM program. The data further characterize the clinical profile of HLP003, which has Breakthrough Therapy Designation from the FDA. This is a routine scientific update with no new binary catalyst or regulatory decision.

Key Facts

  • Four posters presented at Psych Congress 2026 (Sept 15-19, New Orleans) on HLP003, an investigational deuterated psilocin analog for adjunctive MDD treatment.
  • Posters include 12-month efficacy results from the completed Phase 1/2a study and a trial-in-progress overview of the ongoing Phase 3 PARADIGM program.
  • HLP003 has Breakthrough Therapy Designation from the FDA.
  • HLP004 is in Phase 2 for generalized anxiety disorder.
  • Two SC 13D filings by Eric H.L. So and Paul Glavine were filed 12 days prior (Sept 9, 2026), indicating activist interest in Cybin Inc. (Helus Pharma's operating name).

Financial Impact

No financial data disclosed; clinical-stage company with no approved products or revenue.

Risk Factors

  • Phase 3 PARADIGM trial may fail to meet primary endpoints, as is common in MDD adjunctive therapy trials.
  • Regulatory approval is not guaranteed despite Breakthrough Therapy Designation.
  • Activist filings could lead to board changes or strategic shifts, creating uncertainty.
  • Company is pre-revenue and relies on equity financing, diluting existing shareholders.

Investment Themes

Documents Analyzed

This report is based on 1 press release from GlobeNewswire.

DocumentAccession Number
PRESS-RELEASE Data (Synthetic)press-3365383
36 reports for HELP
Performance horizon
50% Hit rate @ T+20 2 of 4 directional calls Went positive at some point 2 of 4 best @ T+20▲ +45.91%Aug 3, 2026
Filters
Rows
Reports for HELP — sortable, filterable
TypeNow
Oct 26, 2026
today
3
NEUTRAL ★ 2/10
$10.11awaiting T+20—$10.19 (+0.79%)
Oct 26, 2026
today
3
NEUTRAL ★ 2/10
$10.86awaiting T+20—$10.19 (−6.13%)
Oct 23, 2026
3d ago
3
NEUTRAL ★ 2/10
$10.50awaiting T+20—$10.19 (−2.95%)
Oct 23, 2026
3d ago
3
NEUTRAL ★ 2/10
$10.50awaiting T+20—$10.19 (−2.95%)
Oct 23, 2026
3d ago
3
NEUTRAL ★ 2/10
$10.50awaiting T+20—$10.19 (−2.95%)
Oct 23, 2026
3d ago
3
NEUTRAL ★ 2/10
$10.50awaiting T+20—$10.19 (−2.95%)
Oct 21, 2026
5d ago
6-K
NEUTRAL ★ 5/10
$10.50awaiting T+20—$10.19 (−2.95%)
Oct 15, 2026
11d ago
6-K
NEUTRAL ★ 3/10
$11.05awaiting T+20—$10.19 (−7.78%)
Oct 15, 2026
11d ago
Press Release
NEUTRAL ★ 3/10
$11.05awaiting T+20—$10.19 (−7.78%)
Oct 8, 2026
18d ago
6-K
NEUTRAL ★ 4/10
$10.72awaiting T+20—$10.19 (−4.94%)
Showing 10 of 36

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Market Closed — Opens Wed (12h 29m)

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Report published Sep 21, 2026