Northwire Canada EditionFriday, July 10, 2026
Northwire
FCI 0.400 −9.1% GR 0.075 +0.0% AII 22.35 +7.5% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0% OGN 3.45 +2.1% MSA 6.28 −2.3% SGZ 0.045 +0.0% S 0.135 +12.5% GRSL 0.310 −3.1% DEX 0.390 +1.3% WMS 0.040 +0.0% EMPR 0.840 +2.4% SAGA 0.480 +0.0% ABX 51.59 −1.2% FCI 0.400 −9.1% GR 0.075 +0.0% AII 22.35 +7.5% TUNG 1.72 +1.8% LGO 1.01 −2.9% EMM 0.080 +0.0% OGN 3.45 +2.1% MSA 6.28 −2.3% SGZ 0.045 +0.0% S 0.135 +12.5% GRSL 0.310 −3.1% DEX 0.390 +1.3% WMS 0.040 +0.0% EMPR 0.840 +2.4% SAGA 0.480 +0.0% ABX 51.59 −1.2%
Earnings Routine +

Helus Pharma Reports Recent Business Highlights and Fiscal Year 2026 Financial Results

Helus Pharma burns cash faster in Phase 3 ramp but secures $50M runway as HLP003 nears topline readout

Executive Summary
  • Helus Pharma reported audited financial results for the fiscal year ended March 31, 2026, showing a net loss of $148.0 million ($47.0 million in Q4), compared to $81.6 million in the prior year.
  • Cash-based operating expenses (R&D, G&A) rose to $131.7 million for the year ($42.6 million in Q4), reflecting the operational scaling required for Phase 3 execution.
  • Cash flows used in operating activities were $133.3 million for the year ($37.3 million in Q4).
  • The company closed a $50 million underwritten equity offering on June 25, 2026, at $4.85 per share, bringing total cash to $157.3 million as of March 31, 2026.
  • Pipeline updates indicate the HLP003 (MDD) APPROACH Phase 3 trial has surpassed 88% enrollment, maintaining the Q4 2026 topline data timeline.
  • HLP004 (GAD) reported positive Phase 2 signal detection results, showing clinically meaningful improvement over standard of care.
  • Leadership transition: Eric So returns as Interim CEO following Michael Cola's departure in April 2026.
Material Impact
  • The $50 million capital raise is a standard, expected financing move for a clinical-stage biotech funding pivotal trials. It extends the cash runway but introduces near-term dilution.
  • The widening net loss ($148M vs $81.6M) and accelerated cash burn are consistent with the planned ramp-up of Phase 3 clinical operations and do not indicate operational mismanagement.
  • HLP003 enrollment at >88% de-risks the Q4 2026 catalyst and confirms execution capability. HLP004's positive Phase 2 data provides a secondary commercial option but does not alter the primary valuation driver.
  • The CEO transition introduces governance uncertainty, but the return of the co-founder mitigates immediate strategic disruption.
HELP · Price
Company Overview
  • Helus Pharma (formerly Cybin Inc.) is a clinical-stage pharmaceutical company developing proprietary novel serotonergic agonists (NSAs) for mental health conditions, primarily Major Depressive Disorder (MDD) and Generalized Anxiety Disorder (GAD).
  • Lead asset HLP003 is in Phase 3 development for MDD, holding FDA Breakthrough Therapy designation.
  • HLP004 is in Phase 2 for GAD, utilizing an intramuscular delivery system optimized for clinical scalability.
  • The company operates under a rebranded identity, trading on Nasdaq under the ticker HELP, with a strong IP portfolio protected through 2041.
Read the original news release →

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