Welcome to our dedicated page for Hemostemix news (Ticker: HMTXF), a resource for investors and traders seeking the latest updates and insights on Hemostemix stock.
Hemostemix Inc. (HMTXF) generates news that spans biotechnology, clinical development, and commercialization of autologous stem cell therapy for ischemic disease. The company’s updates frequently center on its VesCell (ACP-01) platform, a patient-derived blood-based stem cell therapy that Hemostemix reports has been studied in multiple clinical trials for peripheral arterial disease, chronic limb threatening ischemia, cardiomyopathies, congestive heart failure, angina, total body ischemia, and vascular dementia.
Investors following HMTXF news can expect regular announcements on clinical milestones, regulatory interactions, and physician-led initiatives. Hemostemix has reported the completion of a Phase II clinical trial in chronic limb threatening ischemia, publication of results in peer-reviewed journals, and presentations of long-term outcomes such as limb preservation, wound healing, and mortality data in severe ischemic patient populations. News items also describe plans for a basket protocol Phase I trial in ischemia-related conditions and a scheduled FDA Pre-IND meeting to review the company’s proposed trial design and regulatory pathway.
Corporate developments are another recurring theme in Hemostemix’s news flow. The company issues releases on non-brokered private placements, stock option grants, and capital raises intended to fund regulatory, clinical, and commercialization activities for ACP-01. It also reports on strategic moves such as a clinic roll-up strategy, including letters of intent to acquire cardiology practices that have experience treating patients with ACP-01, as well as the build-out of patient care and clinical operations roles.
Sector-specific coverage includes Hemostemix’s participation in conferences focused on wound healing, diabetic limb salvage, and regenerative medicine, where the company highlights its CLTI and cardiovascular data. For readers tracking HMTXF, this news page offers a consolidated view of scientific, regulatory, financial, and operational updates related to Hemostemix’s autologous stem cell therapy platform.
Hemostemix (OTCQB: HMTXF) has announced an oversubscribed private placement, raising $2.7 million through a non-brokered offering, exceeding the initial target of $2.5 million. The company is issuing units at $0.10, with each unit comprising one common share and one warrant exercisable at $0.15 for two years.
Chairman Peter Lacey led the placement with a $1.5 million subscription. Additionally, the company has negotiated a debt settlement of $400,000 at $0.20 per share. Proceeds will be used to repay CD#1 and support working capital, including marketing and sales of VesCell™.
Hemostemix (OTCQB: HMTXF) has successfully closed a non-brokered private placement offering, raising CAD $469,366 through the issuance of 3,911,385 Common Shares at CAD $0.12 per share. The TSX Venture Exchange has granted conditional approval for this offering.
The funds will be directed towards general working capital, operational expenses, and business development activities. The issued securities are subject to a four-month hold period under Canadian securities laws. The investor is confirmed to be arm's length to the company and not a Related Party.
Hemostemix (OTCQB: HMTXF) has published its 10th scientific paper detailing ACP-01's molecular strategy for treating heart failure, specifically focusing on non-ischemic dilated cardiomyopathy (DCM). The publication highlights how ACP-01's unique characteristics differentiate it from traditional bone marrow-derived cell therapies.
The company's previous studies demonstrated that cardiac function improved by up to 47.1% after one ACP-01 treatment in DCM patients. ACP-01's effectiveness is attributed to three key mechanisms: precise migration to injured tissue through CXCR4 expression, attraction of Natural Killer cells to reduce inflammation and fibrosis, and improved microcirculation through angiogenesis.
Following Florida's new law permitting non-FDA approved stem cell treatments, Hemostemix is now offering ACP-01 therapy to no-option DCM patients in Florida.
Hemostemix (OTCQB:HMTXF) announced the appointment of Croom Lawrence as Chief Commercialization Officer. The company has partnered with Lawrence to offer MCI Screen, an FDA-approved and insurer-reimbursed advanced cognitive test for Vascular Dementia. The company noted that their ACP-01 treatment has shown clinical success in reversing vascular dementia in one patient for over ten years.
Hemostemix (OTCQB: HMTXF) announced a significant financial restructuring, with Chairman Peter Lacey providing a $1.5 million lead order for a non-brokered private placement at $0.10 per Unit. Each Unit includes one Common Share and one Warrant exercisable at $0.15 for two years. $1.25 million will be used to fully repay a $2.5 million Convertible Debenture.
The placement is part of a larger offering totaling up to $2.5 million. The company also confirmed the conversion price of previously announced ACP-01 Therapy Convertible Debentures (TCD) at CAD $0.155, relating to the March 5 sale of 15 TCDs for $708,605.
Hemostemix Inc. (HMTXF) presented its clinical trial results at the TERMIS 2025 World Congress in Freiburg, Germany. The company showcased its Phase II clinical trial findings, published in JBRES, demonstrating significant improvements in ischemic tissue perfusion, pain reduction, wound healing, and limb salvage in no-option CLTI patients. The presentation also highlighted data from five heart studies investigating ACP-01 in various cardiac conditions.
CEO Thomas Smeenk emphasized the company's revenue generation of >$1 Million to date and discussed their strategy of using therapy convertible debentures sales to fund their phase III clinical trial. The company's autologous blood-based stem cell therapy, ACP-01, has completed seven clinical studies with 318 subjects, showing promising results for various cardiovascular conditions, with notably 0% mortality and 83% wound healing rates in CLTI patients.
Hemostemix (OTCQB: HMTXF) has completed a non-brokered private placement of USD $336,500, issuing 1,634,466 common shares at CAD $0.295 per share to CytoImmune Therapeutics LLC. The proceeds will be used for general working capital and business development activities.
The company is an autologous stem cell therapy platform developer that has completed seven clinical studies involving 318 subjects. Their lead product, ACP-01, has shown significant results in treating various conditions including peripheral arterial disease and chronic limb threatening ischemia (CLTI). Notable results from their Phase II CLTI trial showed 0% mortality and wound healing in 83% of patients, compared to the typical 60% five-year mortality rate.
[ "Successful completion of USD $336,500 private placement for working capital", "Strong clinical trial results with 0% mortality rate in CLTI patients vs. industry standard 60%", "83% success rate in wound healing for patients followed up to 4.5 years", "Extensive clinical experience with 7 completed studies involving 318 subjects" ]Hemostemix Inc. (HMTXF) will participate in Invest Stuttgart 2025, Germany's leading finance and investment conference, from May 9-10, 2025. The company specializes in autologous stem cell therapies, with its flagship product ACP-01 treating various cardiovascular conditions. The therapy has demonstrated safety and efficacy across 498 patients and seven clinical studies.
The company has introduced ACP-01 Therapy Convertible Debentures (TCDs) as an innovative financing instrument, offering 6% annual interest payable in shares. TCDs can be converted into either ACP-01 therapy or common shares. Hemostemix has already sold over CAD $1.14 million of TCDs, supporting revenue forecasting and treatment scheduling.
Hemostemix Inc. (TSXV: HEM) (OTCQB: HMTXF) has partnered with PatentVest, a subsidiary of MDB Capital, to strengthen its global patent portfolio in autologous stem cell therapy for cardiovascular diseases. PatentVest will provide comprehensive IP support including:
- Evaluation and optimization of existing patents
- Identification of new patentable therapeutic innovations
- Development of global filing strategies
- Enhancement of company value for strategic partnerships
PatentVest will accept partial payment in equity, aligning with shareholder interests. The partnership aims to extend patent terms based on ongoing FDA studies and leverage the company's automated bioreactor technology license to reduce production costs and improve treatment accessibility.