Curated News
By: NewsRamp Editorial Staff
June 12, 2026
Helix BioPharma Reports Reduced Loss, Builds Cash for U.S. Listing
TLDR
- Helix BioPharma raised $3.7M and plans a U.S. exchange listing, boosting access to capital and investor base.
- Helix reduced net loss to $671K for Q3 2026, raised funds via convertible debentures, and advanced L-DOS47 towards clinic.
- Helix aims to make hard-to-treat cancers vincible with innovative therapies like L-DOS47 and oral prodrugs.
- Helix is developing an oral gemcitabine prodrug, GEMCEDA, with bioavailability comparable to IV administration.
Impact - Why it Matters
This news matters because Helix BioPharma is advancing promising cancer therapies like L-DOS47, which could transform treatment for hard-to-treat cancers such as non-small cell lung cancer. The company’s improved financial health and plans for a U.S. exchange listing signal potential growth and increased access to capital, which could accelerate clinical development. For investors and patients, this represents a step toward bringing innovative oncology solutions to market, potentially expanding treatment options and improving outcomes for those with limited alternatives.
Summary
Helix BioPharma Corp., a clinical-stage oncology company listed on TSX under “HBP,” OTC PINK as “HBPCD,” and FRANKFURT as “HBP0,” has announced its financial results and filed its unaudited interim financial statements for the three- and nine-month periods ended April 30, 2026. The company, led by CEO Thomas Mehrling, MD, PhD, reported a net loss of $671,000 for the quarter (down from $1,544,000 in the prior year) and $2,374,000 for the nine-month period (vs. $4,255,000 previously). The reduced loss was attributed to lower R&D expenses and the closure of the LDOS006 study. Cash reserves rose significantly to $2,842,000 from $65,000 at July 31, 2025, bolstered by $3,673,000 in proceeds from a private placement of unsecured convertible debentures, which carry 25% annual interest and mature in July 2027. The principal is convertible at $1.42 per share, and accrued interest is convertible at the greater of $1.42 or the 5-day VWAP less the TSX-permitted discount. The company is also exploring a U.S. exchange listing to broaden its investor base and access to capital.
Helix’s pipeline focuses on hard-to-treat cancers, with lead candidate L-DOS47, a Tumor Defense Breaker antibody-enzyme conjugate targeting CEACAM6-expressing tumors. L-DOS47 has completed Phase Ib studies in non-small cell lung cancer (NSCLC) and underpins next-generation bispecific antibody-drug conjugates (ADCs). The company also advances pre-IND candidates: LEUMUNA, an oral immune checkpoint modulator for post-transplant leukemia relapse, and GEMCEDA, a first-in-class oral gemcitabine prodrug with bioavailability comparable to IV administration. These innovations aim to expand treatment options for advanced cancers. The Interim Filings are available on SEDAR+ and the company’s website, as noted in the original release. Helix is working with legal advisors on a base shelf prospectus and engaging investment banking partners for future financing, while assessing opportunities to increase access to U.S. capital markets, including a potential listing on a U.S. securities exchange.
The company’s strategic priorities include advancing L-DOS47 toward the clinic and creating long-term shareholder value. The financial results demonstrate improved cash position and reduced losses, signaling progress toward operational stability. With the successful private placement, Helix aims to secure approximately twelve months of operating runway. The company’s focus on securing capital and expanding its investor base underscores its commitment to developing novel cancer therapies. For more details, the original release can be viewed on the NEWMEDIAWIRE.
Source Statement
This curated news summary relied on content disributed by NewMediaWire. Read the original source here, Helix BioPharma Reports Reduced Loss, Builds Cash for U.S. Listing
