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HELPNasdaq

CYBIN INC.

Pharmaceutical preparations·Phase 3·Toronto, ON, Canada·CEO: Mr. Michael I. Halstead J.D.
NeurologyPsychiatry

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Prepared research question

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BioSniper AI · HELP

Cybin Inc., now operating as Helus Pharma (NASDAQ: HELP), is a clinical-stage biopharmaceutical company developing psychedelic-based therapies for psychiatric disorders, with lead candidate HLP003 in Phase 3 trials for major depressive disorder.

Key risk: Clinical trial failure risk

8.9/10

BioSniper Score

Based on 2 of 6 signals

Limited data coverage

Market Cap

$889.9M

Cash Runway

Lead Asset

Financial data as of Mar 31, 2025.

Tracking 4 clinical trials · 3 catalysts for CYBIN INC..

AI OverviewAI overview is shown in English only.

Cybin Inc., now operating as Helus Pharma (NASDAQ: HELP), is a clinical-stage biopharmaceutical company developing psychedelic-based therapies for psychiatric disorders, with lead candidate HLP003 in Phase 3 trials for major depressive disorder.

  • Cybin rebranded to Helus Pharma and relisted on Nasdaq under ticker HELP in January 2026 [news · 2026-01-11].
  • Lead candidate HLP003 has FDA Breakthrough Therapy designation for major depressive disorder and is in Phase 3 trials [news · 2026-01-11].
  • Cash and equivalents were $135.0M as of 2025-03-31 [sec].
  • Shareholders' equity was $48.2M as of 2025-03-31 [sec].
  • The company filed a $100,000,000 at-the-market follow-on equity offering of common shares [news · 2026-01-11].

What works

  • HLP003 has FDA Breakthrough Therapy designation, which may expedite development and review [news · 2026-01-11].
  • The company has a cash position of $135.0M as of 2025-03-31, providing runway for ongoing Phase 3 trials [sec].
  • Jefferies initiated coverage with a Buy rating, highlighting psilocybin therapies as key growth drivers [news · 2026-02-19].

What to weigh

  • The company has an accumulated deficit and is not yet profitable, typical for clinical-stage biotechs [sec].
  • Phase 3 topline results for HLP003 are not expected until September 2026 at the earliest, creating a long wait for potential catalysts [catalyst].
  • The company faces competition from established players like Pfizer and Eli Lilly in the major depressive disorder space [competitor_trial].
  • The stock dropped 9.1% after the rebranding and Nasdaq relisting, suggesting market skepticism [news · 2026-01-11].

From the filings

Quoted directly from source documents.

  • Cybin rebranded to Helus Pharma and relisted on Nasdaq.

    Cybin Inc., now operating as Helus Pharma, has rebranded and moved its U.S. listing from NYSE American to Nasdaq under the ticker HELP

    News · January 11, 2026

  • HLP003 has FDA Breakthrough Therapy designation.

    FDA Breakthrough Therapy-designated Phase 3 candidate HLP003 for major depressive disorder

    News · January 11, 2026

Catalyst timeline

  • 2026-09-01 · Phase3_ToplineTopline results from a Phase III placebo-controlled trial of CYB003 (HLP003) for major depressive disorder, measuring MADRS endpoint.
  • 2027-05-08 · Phase3_ToplineTopline results from a second Phase III study comparing HLP003 to control in major depressive disorder, measuring MADRS.
  • 2028-03-15 · Phase3_ToplineTopline results from a long-term extension trial of HLP003 assessing safety and optional additional doses.
Risks & what to watch (4)

Key risks

  • Clinical trial failure riskPhase 3 trials for HLP003 may fail to meet endpoints, leading to significant stock decline [catalyst].
  • Cash burn and dilutionWith $135M cash but no revenue, the company may need further financing, diluting shareholders [sec].
  • Competitive landscapeMajor depressive disorder is crowded with competitors like Pfizer, Eli Lilly, and Biohaven [competitor_trial].
  • Regulatory and market adoptionPsychedelic therapies face regulatory hurdles and stigma, potentially limiting commercial uptake [news].

What to watch

  • Phase 3 topline results for HLP003 expected September 2026 [catalyst].
  • Additional Phase 3 readouts for HLP003 in May 2027 and March 2028 [catalyst].
  • Progress of HLP004 for generalized anxiety disorder [news · 2026-01-11].
  • Any updates on the at-the-market equity offering and cash runway [news · 2026-01-11].

Sources: Catalysts · Competitor trials · News · Generated August 20, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 2 of 6 signals · derived from public data

No clinical pipeline tracked — this score reflects financial & catalyst signals only.

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.7

D/E 0.09

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum8.0

3 upcoming, next in ~2d

Insider SignalN/A

No insider transactions in the last 180 days

Catalysts

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

79

Total value held

$92.0M

Showing top 10 of 79 institutional holders of CYBIN INC.. Open the full 13F history after sign-in.

Frequently asked questions

What is the AI investment thesis for CYBIN INC.?

Cybin Inc., now operating as Helus Pharma (NASDAQ: HELP), is a clinical-stage biopharmaceutical company developing psychedelic-based therapies for psychiatric disorders, with lead candidate HLP003 in Phase 3 trials for major depressive disorder.

What is CYBIN INC.'s next catalyst?

CYBIN INC.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A Phase III, Placebo-Controlled, Randomized, Double-Blind Trial of Oral Doses of CYB003 to Assess Co" — expected September 1, 2026.

Who is the CEO of CYBIN INC.?

Mr. Michael I. Halstead J.D. is the chief executive officer of CYBIN INC. (HELP).

Where is CYBIN INC. headquartered?

CYBIN INC. (HELP) is headquartered in Toronto, ON, Canada.

What therapeutic areas does CYBIN INC. focus on?

CYBIN INC. develops therapies across Neurology, Psychiatry.

925 companies232,681 SEC filings21,419 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.