Northwire Canada EditionWednesday, July 15, 2026
Northwire
EFF 0.030 +20.0% W 0.500 +1.0% RDG 0.160 +0.0% ARIC 0.780 +4.0% VROY 3.44 +5.2% ROCK 3.81 +3.0% APMI 0.120 +0.0% EM 3.58 −4.8% ALS 66.04 +6.8% MEK 0.065 +44.4% TLO 6.00 +13.0% ADE 0.045 −66.7% FAIR 0.060 +33.3% SVRS 0.420 −2.3% RES 0.050 +42.9% CYG 0.120 +0.0% EFF 0.030 +20.0% W 0.500 +1.0% RDG 0.160 +0.0% ARIC 0.780 +4.0% VROY 3.44 +5.2% ROCK 3.81 +3.0% APMI 0.120 +0.0% EM 3.58 −4.8% ALS 66.04 +6.8% MEK 0.065 +44.4% TLO 6.00 +13.0% ADE 0.045 −66.7% FAIR 0.060 +33.3% SVRS 0.420 −2.3% RES 0.050 +42.9% CYG 0.120 +0.0%
Earnings

Helix BioPharma Corp. Announces Fiscal 2025 Year-End Results

HBP · Price

Executive Summary

  • Helix BioPharma reported FY 2025 net loss of $5.205 M (loss per share $0.09), an improvement from the prior year’s $9.264 M loss.
  • The company refocused its pipeline on L‑DOS47 combined with pembrolizumab for first‑line NSCLC and terminated collaborations outside this scope.
  • Completed a non‑brokered private placement of 2,222,333 shares at $0.75 (gross proceeds $1.667 M) and closed a $3.0 M private placement earlier in the year; also issued 125,000 shares for option exercises ($113 k).

Key Details

  • Financial Results FY 2025 (ended July 31, 2025)
  • Net loss: $5,205,000 (vs. $9,264,000 in FY 2024)
  • Loss per common share: $0.09 (vs. $0.21 loss/share FY 2024)
  • Working‑capital deficiency: $2,807,000
  • Shareholders’ deficiency: $15,586,000
  • Accumulated deficit: $215,876,000

  • Research & Development

  • R&D expense FY 2025: $3.558 M (down 40% YoY) – reflects completion of Phase Ib/II pancreatic study and reduced third‑party collaborations.
  • Ongoing clinical programs:

    • LDOS006 (Phase Ib/II in metastatic pancreatic adenocarcinoma) completed Oct 2024; CSR expected Fall 2025.
    • LDOS007 – new Phase Ib/IIa NSCLC study planned; FDA written feedback received Aug 8 2025, allowing the company to skip the scheduled videoconference and proceed with CTA preparation.
  • Strategic Refocus

  • Decision to concentrate on L‑DOS47 + pembrolizumab for first‑line NSCLC, based on unmet need and shortest path to FDA approval.
  • Terminated research collaborations with University of Tübingen (Aug 9 2024) and Peter Mac (Aug 13 2024).
  • Closed Edmonton laboratory (Oct 31 2024) and liquidated equipment; retained samples/documents with third‑party storage.

  • Corporate Development & Financing

  • Equity Draw‑down Facility: Announced on Sep 5 2025 that the previously announced GEM facility will not be pursued.
  • Private Placement (Aug 22 2025): 2,222,333 common shares @ $0.75 → $1.667 M gross proceeds.
  • Earlier Private Placement (Jan 8 2025): 4,000,000 common shares @ $0.75 → $3.0 M gross proceeds, with a 10% finder’s fee paid.
  • Option Exercise (Apr 21 2025): Issued 125,000 common shares for cash $113,000.

  • Acquisitions

  • Laevoroc Asset Acquisition (May 20 2025): Acquired assets & certain liabilities of Laevoroc Immunology AG and Laevoroc Chemotherapy AG in exchange for:

    • 11,555,076 common shares (fair value $9.88 M)
    • 9,454,153 common shares (fair value $8.083 M)
  • Leadership Changes

  • CEO appointment: Thomas Mehrling, MD, PhD (effective Apr 10 2025).
  • COO appointment: Veronika Kandziora (Apr 24 2025).
  • CFO appointment: Rohit Babbar (Jun 2 2025), replacing James B. Murphy.

  • Liquidity Outlook

  • Cash on hand as of July 31 2025: $65,000, insufficient to fund working capital and R&D for the next twelve months; management prioritizing additional equity financing.

Notable Quotes

“Our strategic refocus on L‑DOS47 combined with pembrolizumab positions us to address a critical unmet need in NSCLC while accelerating our path toward FDA approval,” – Thomas Mehrling, CEO.

Read the original news release →

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